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Collection of 900+ MCQs based on NCERT Bl an CHEMISTRY improves | CY 0 | =m by at least eee ey cen 0, based — 20% |e DAILY PRACTICE PROBLEM DPP CHAPTERWISE CCO1 - CHEMISTRY 2 Total Questions Total Marks © |Attempted Correct = Incorrect Net Score 5 Cut-off Score 37 Qualifying Score a Success Gap = Net Score — Qualifying Score Net Score = (Correct x 4) — (Incorrect x 1) Bl a CHEMISTRY Dae Daily Practice Problems Collection Improves ae of 900: your Score CHEMISTAY Ve Qs by at least Chapters TS any based 2 0 % apie on NCERT ILY PRACTICE PROBLEM DPP CHAPTERWISE CCO SUAS 2 Total Questions 30 Total Marks 120 Attempted | [correct [Net Score Incorrect Cut-off Score Scoring G + Corporate Office : 45, 2nd Floor, Maharishi Dayanand Marg, Comer Market, ‘Malviya Nagar, New Delhi-110017 Tel. :011-49842349 / 49842350 De ers[e] cy ‘Typeset by Disha DTP Team DISHA PUBLICATION ALL RIGHTS RESERVED © Copyright Publisher ‘No part ofthis publication may be reproduced in any form without prior permission of the publisher. 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For further information about books from DISHA, Log on to www.dishapub! cation,com or email to info@dishapublication,com GP_3371 INDEX/CHAPTE Page No, BASIC CONCEPTS OF CHEMISTRY ca - ca ATOMIC STRUCTURE cs - 6-8 DEE cuSsIricaTion OF ELEMENTS AND PERIODICITY IN PROPERTIES c9- 0-12 CHEMICAL BONDING AND MOLECULAR STRUCTURE c13_- 6-16 STATES OF MATTER c-17 ~ c-20 THERMODYNAMICS cn - 624 BGM counsrum 6-25 - ¢-28 REDOX REACTIONS 6-29 - 0-32 HYDROGEN 6-33 - 6-36 S-BLOCK ELEMENTS c-37 ~ ¢-40 BLOCK ELEMENTS (Gp-13 414) coat = Coad GENERAL ORGANIC CHEMISTRY cas ~ c-48 HYDROCARBONS c-a9 ~ 6-52 ENVIRONMENTAL CHEMISTRY c-53 - 6-56 SOU STATE c-87 - €-60 SOLUTIONS C-61 - C64 ELECTROCHEMISTRY C65 ~ ¢-68 CHEMICAL KINETICS c-09 - ¢-72 SURFACE CHEMISTRY c-13 ~ 6-76 GENERAL PRINCIPLES AND PROCESSES OF ISOLATION OF ELEMENTS c-17 ~ ¢-80 THE p-SLOCK ELEMENTS (GROUP 15. 16, 17 & 18) c-01 ~ c-84 THE d-AND F-BLOCK ELEMENTS C05 - c-88 COORDINATION COMPOUNDS c-09 - c.92 HALOALKANES & HALOARENES 6-93 - ¢-96 ALCOHOLS, PHENOLS, ETHERS €-97 - ¢-100 ALDEHYDES, KETONES AND CARBOXYLIC ACIDS €-101 = ¢-104 AMINES: €-108 - ¢-108 BIOMOLECULES c-109 - 6-112 POLYMERS c-118 - 6-116 CHEMISTRY IN EVERYDAY LIFE c-117 - ¢-120, Solutions To Chapter-wise DPP Sheets (1-30) S-1 - S-64 MOCK TEST FULL SYLLABUS 1-8 ic] Purchase BONNE e<25/- Visit : http://bit.ly/2ZA5UqWt Pease . A Cnn es ONC m el Mock Tests Key Features : Online Mock test on Exam Format + Instant Result + Detailed Analysis Performance Tracker Improves strike rate! speed + Gives Real Exam-like feeling Purchase BONNE @25/- Visit : http://bit.ly/2A9DCfc BITSAT Exes once ae a emery SEs Mock Tests Key Features : Online Mock test on Exam Format + Instant Result Detailed Analysis Performance Tracker Improves strike rate/ speed + Gives Real Exarr-like feeling GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time = End CHEMISTRY (Cco1 ‘SYLLABUS : Some Basic Concepts of Chemistry Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Daly Practice Problem Sheet contains 30 MCQ's, For each question only one option is correct Darken the correct cicle/ bubble in the Response Grid provided on each page, 1, In compound A, 1.00g of nitrogen unites with 0578 of oxygen. In compound B, 2.00g of nitrogen combines with 2.248 of oxygen In compound C, 3.00g of nitrogen ‘combines with 5.11g of oxygen. These results obey the following aw (@ law of constant proportion (b) law of multiple proportion. (©. lawof reciprocal proportion (@) Dalton’ aw of partial pressure 2. 10° molecules are removed from 200mg of CO,. Themes oF CO, let re (@) 288109 () 288x103 (©) 288x108 @ 88x10" ‘What volume of hydrogen gas, at 273 K and | atm. pressure will be consumed in obtaining 21.6 g of elemental boron (atomic mass = 10 8) from the reduction of boron trichloride by hydrogen ? @ OL © 4aL © 2aL © 96. [Number of of oxygen in 32.2 gNa,S0, 10H,Ois @ m3 2% © 24 © 208 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work s. 10. 6.02 x 10° molecules of urea are present in 100 ml ofits solution. The concentration of urea solution is @ 00M ©) 001M © 001M @ 01M (Avogacocanctant, N= 6.02 102? mot-!) I we consider that 1/6,in place of 1/12, mass of carbon stom istaken tobe the relative atomic mass unit, the mass of one mole ofthe substance wil (@) bea function ofthe molecular mass ofthe substance (©) remain unchanged (© increase two fold (@) decrease twice ‘The weight of NaCl decomposed by 4.9g of H,$0,.if6 of sodium hydrogen sulphate and 1.825 g of HCl, were produced in the reaction is @ 6921 ©) 4658 © 2925¢ @ 14g Which one ofthe following isthe lightest? (@) 0.2 mole ofhydrogen gas (©) 6.023% 1022 molecules of nitrogen © Ol gofsitver (@) 0.1 mole of oxygen gas How many moles of magnesium phosphate, Me,(PO,), will contain 0.25 mole of oxygen ators? (@) 125102 ©) 25x10 © 0@ (@ 3125x102 ‘The density (in gmL~! of 3.60 M sulphuric acid solution that is 29% H,$0, (molar mass= 98 go! by mas willbe 2 DP C01 @ 14s ) Lot © 188 @ 12 AL. A gas occupies a volume of 300 ce at 27°C and 620 mm, pressure, The volume of gas at 47°C and 640 mm pressure (@) 260ce ©) 310ee (©) 390ce @ 450ce 12, Haemoglobin contains 0.33% of iron by weight. The ‘molecular weight of haemoglobin is approximately 67200. ‘The numberof iron atoms (at. wt. of Fe = 56) present in one molecule of haemoglobin is @ 6 m1 ©2 @ 4 13, The volume of 20 volume H,O, required to get Slitres of O, atSTPis (@) 250ml © 100ml 14, Inthereaction, &) 125ml (@) 50m 2Al(s)+ 6HCI(aq) > 2AK**(aq) +6CT” (aq) +3H2(8) (@) 112LH,e) atSTPis produced for every mole HCKaa) consumed (©) 6LHCIag) is consumed frevery 3 Hyg) produced (©) 33.6LH,6)is produced regardless of temperature and Pressure for every mole Al that reacts (@) 672118) at STP is produced for every mole Al that reacts an 5. @0O@ 6 @OO@ 1.@@O@_U.@OO@ 7. @0O@ §& @O0OOO % Q0O@ 12.@@O@_13.©@OOO_14. @OOO ‘Space for Rough Work GP_3371 DPP/ CC01. ———— asl 18. 16. aw. 18. 1». 20. 20.@@O@_21.©@OO@ 2.@©OO_23.@OOO@_¥%4. @OOO “Theconcentrated sulphuric acd thats peded commercial On complete eaction with excess HCI, one kilogram ofthe is 959 H,SO, by weight Ifthe density ofthis commercial __ washing sod wil evolve ‘acids 1.834 gor, the molarity ofthis solution is (@ SmolefCo, ©) L6molofco, @ 178M © 120M © 17molefCo, @ 18moloéco, © 105M @ 157M 21. Arrange the numbers in increasing no. of significant figures. What isthe mass of precipitate formed when SOmLof 169% "Goongang, 2460240 solution of AgNO, is mixed wih SOmLof5.8% NaCI solution? (Ag= 107.8, N= 14,0= 16, Ne 3, C1= 35.5) ed @ Be ©) 358 (©) 2.6000<26.<0.002600.<0.250 Os @ us (©) 0260<2.6<0.0m600.<2.6000 ‘Number of valence electrons in 42 gram of N;~ionis (©) 0.002600 <0.260<2.6<2.6000 @ 42Nq (©) ON, 22,_ Dissolving 120 of compound (mol wt. 60) in 1000 g of © isn, @ 32N, ‘water gave a solution of density 1.12 g/mL. The molarity of Atransition metal M forms a volatile chloride which has a pe eolurioe is ‘vapour density of94.8 Iitcontains 74.75% ofchlornethe _-(@)_-1.00M © 200M formula of the metal chloride wil be © 250M (® 400M @ MO; ©) MC, 23, gaseous compound of nitrogen and hydrogen contains © MO, @ MO, 12.5% (by mas) of hydrogen, The density ofthe compound ‘A gaseous hydrocarbon gives upon combustion 0.72 g of relative to hydrogen is 16. The molecular formula of the ‘water and 3.08 g. of CO>. The empirical formula of the ‘compound is: hydrocarbon is @ NH, ©) NH @ CM, © CH, © NI, © Ny © Cells @ GH, 24, The amount ofBaSO, formed upon mixing 100ml of 20.8% Following isthe composition ofa washing soda sample BACI, solution with 50 mL. of 9.8% H,S0, solution with “Substance ___Molecular Wt. __ Mass percent 50 mL of 9.8% H,SO, solution will be: NaC, 1050 us (Ba=137,C1=355,5=32,H= 1 andO=16) NaHCO, 840 84 @ 238 ©) 1165 Nc. sas 68 © 3068 © 3328 5.@OQO@ 6.@OOO 17.@O0OO 18.@OQO@ VY. @O0OO@ ‘Space for Rough Work bes ——— DPR CC 25, 2g ofa mixture of CO and CO, on reaction with excess 1,0, produced 2.54 g of Ip. What will be the mass % of CO, in the original mixture? @ 3s © » ©» @ o 26, 7.5 grams of a gas occupy 5.6 litres of volume at STP. The gas is @ NO ©) NO © co @ ©, 27. Number of moles of KMnO, required to oxidize one mole of Fe(C,0,)in acidic medium is (@) 0167 ©) 06 © 02 @ 04 28. What is the weight of oxygen required for the complete ‘combustion of 2.8 kg of ethylene ? 29, (@) 28kg ©) 6tkg © 96kg @ 96kg ‘A gus mixture of 3 lites of propane (C;Hg) and butane (CHjo) on complete combustion at 25° C produced 10 lie CO. Find out the composition of gas mixture (Propane : Butane) @ 2:1 © 1:2 © 15:15 @ 05:25 ‘An organic compound contains 49.3% carbon, 6.84% Ihydrogen and its vapour density is 73. Molecular formula ofthe compound is (@) C\H,O, (b) CH yO, © CoH @ CHO, LE OOOO %©OQOO 27.@OOO BOOOO % OOOO @QO@ PROBLEM Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 37 Qualifying Score 52 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time = End Time : CHEMISTRY (Cco2 ‘SYLLABUS : Structure of Atom Max. Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. Among the following groupings which represents the 3. The de-Broglie wavelength of an electron in the ground collection of isoelectronic species? state of hydrogen atom is : (KE, = 136 eV: leV = @ NO*,CH.03,CO ©) Np, C},CO,NO Pee @) 328m (b) 3328nm © CO, NO*, CN-,C} @_NO,CN~,N>,03 (© 03328nm (@) 00332nm 4. The frequency of light emitted for the transition n = 4 t0 n= 2 of the He* is equal to the transition in H atom, corresponding to which of the following ? (@ n=2t0n=1 @) n=3t0n=2 © n=4t0n=3 @— n=3t0n=1 2 Thecompound in which cation i isoelectronic with anion @ Na () CF © Nal @ KS 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work bes ——— —. DPR C02 5 2 9% 10. ‘The first emission line in the atomic spectrum of hydrogen in the Balmer series appears at TR ogy hl © Rem aR SR Row @ Ben In hydrogen atomic spectrum, a series limit is found at 12186.3 cm”, Then it belong to @ Lyman series (b) Balmer series (© Paschen series (@) Bracket series ‘Two fast moving particles X and Y are associated with de Broglie wavelengths 1 nm and 4nm respectively. mass ‘Xin ine mes the mass OFY, the ato of kinetic energies of Xand ¥ would be © @ 31 ©) 9:1 © 5:12 © 16:9 ‘Theratio of magnetic moments of Fe) and Co(tis @ 73 () 3:7 © WB @ Viv ‘The values of Planck's constant is 6.63 x 10 Js, The velocity of light is 3.0 108 ms, Which valueis closest to the wavelength in nanometre of a quantum of light with frequency of 8 1015 s-!9 @ 5x10 @) 4x10! © 3x10 (@ 2x10 Li and a proton are accelerated by the same potential, their de Brogiewavdengths 2, and 2, have the ratio (assume ms=9m) @ 1:2 © 14 Oe @ 1:33 U1, Energy levels, 4, B, C, of a certain atom correspond to increasing values of energy Le. 4 < By < EI. hy are the wave lengths of radiations corresponding to the transition from Cto B, Bto A and CtoA respectively, which of the following statements is correct?” a (@) 15=%y4%q © yey @ 321203 12. Iuncertainty in position and momentum are equal, then ‘uncertainty in velocity is wo tf 7 of h ® oe ; of 13. Theelectrons, identified by quantum numbers n and 1) .1= 1 Gi) n= 4,1=0 Gi) n= 3,1=2Gyyn=3, 1 I can be placed in order of increasing energy, from the lowest to highest as @) G Mg? > AP* eee 2. The van der Waal and covalent radii of fluorine atom << respectively from the following fgureare © FsOhSe> Te;electronegativi 8pm Tap a ee 1. @0OO_2 @©OOO_3. OOOO _4 OOOO ‘Space for Rough Work 1¢-10- —————_—_—________________- DPP/ CC03 5 2 In which ofthe following arrangements, the order is NOT ‘according tothe property indicated against it? (@) LiS0,>CO>CO, (6) N0,>80,>C0, >CO (© 80,>CO,>CO>N,0, (@_0,>N,0,>CO>CO, ‘The correct order of ionization energy for carbon, nitrogen ‘and oxygen atoms is: (@) C>N>0 ) CoN0 @ CF>F>0 () F>0*>F>0 © OF >0>F >F @ OF > >05F 11. Whichofthe following has the maximum number of unpaired electrons? (@) Mg © TH ow @ Fe 12, Theincorrect statement among the following is (@) Thefirst ionization potential ofl sess than the ist ionization potential of Mg (©) The second ionization potential of Mis greater than the send ionization potential of Na (©) Thefistionization potential ofNaislessthan the ist ionization potential of Mg (© Thethird ionization potential of Mgis greater than the third ionization potential of AL 13, According to the Periodic Law of elements, the variation in properties of elements isrelate to their (@) nuclear masses ©) atomic numbers (©) nuclear neatron-proton number aos (@)_stomic masses 14, Identify the correct order ofthe sizeof the following (@ Ce @ Ce eK cares Ci>Br>1 (b) Cl>F>Br>1 @ OF ) OF

(©) Br>Cl>I>F @) [>Br>Cl>F @ N3<0%

Oe Ay 141 Kira these are respectively O° (@) +e 0% (@; AH? =+780 KI mor! (@ Tand ©) Vanat “Thus proces of formation of O in gas phaseis unfavourable (©), Wand (®) andy ‘even though OF- is isoelectronic with neon, It is due tothe 29+ Consider the following statements aces (0 Atomic radi decreases across row of the periodic table when we move from left o right Atomic radii increases down the column as we move, fiom top to bottom. (@) Electron repulsion outweighs the stability gained by achieving noble gas configuration (&) ©" ier has comparatively smaller sizethan oxygen atom jy_Although the order of elements is based on atomic ©) Oxygen is moreclectronegative numbers, vertical families share similar chemical (@ Addition of electron in oxygen results in larger size of properties, theion, Which ofthe satement) given above iae conse? 27, Which of the following statementsis wrong ? @ @anaciy () @andGid (@) vander Waa'sradiusofiodineismerethanitscovalent (©) Gi)and Gi) (@ @.Giand Gi radius 30, Match Colum with Columa-tt and selet the correct, ) Al soeeot telong to same period of the answer bythe given codes, perio table Calaroe-L Colurntt (©) TE, of Nis higher than that of O while LE. of is (Atoms) (Properties) higher than that of N e (> Hie ckroneznve ) F @)_ Most clectropositive (d)_ The electron gain enthalpy of N is almost zero while Si thaofPis7431d mol" © (©) Swongest reducing agent 28. The first (A\H,) and second (A,H) ionization enthalpies by Highest ionisation energy Gin kJ mot!) and the electron gain enthalpy (S,yH) ; Goan aceaain nwa one) a 8 OE BES ES PI 25.O00O0 2%. OOOO 27.O0O0O 8OOOO 2 OOOO cr 30.©OOO Raa Nees Total Questions Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 38 Qualifying Score 55 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End CHEMISTRY (cco4 ‘SYLLABUS : Chemical Bonding and Molecular Structure Max. Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 11. Which ofthe following does not contain coordinate bond? @ BAY NEY © cof @ 10° 2. Which ofthe following has the highest dipole moment? cH i. b N ti @ —e-0 ® C=C He Tt ch eh © ¢ ¢ @ ere (Of the folowing hydrides which one has the lowest boiling point ? (@) ASH; —() SbH; (© PH; — @ NH; In compounds of type ECI,, where E = B, P. As or Bi, the angles Cl-E- Cl for different Earein the order. (@) B>P=As (©) B>P>As>Bi (©) B&P=As=Bi (@) BePeAs the dissociation energy of 0-O bond, G@) increases, decreases () decreases, increases (©) decreases in both cases (@ increases in both cases 8% According to MO theory which ofthe following lists ranks the nitrogen species in terms of increasing bond order? @ NE bondir~ 9, The dcresing vals of tnd anges tom NH 106) 0 nd pair ‘SbH, (101°) down group-15 ofthe periodic table is due to Jone pair- lone psi > bond pir -bondpair> lone pair (© lene ir tone pair-bondpuir>lonepair 4) “Yereasng ip-bp repulsion (© bond pair - bond pair > lone pair - bond pair > lone pair (b) decreasing electronegativity lone pair (©) increasing bp-bp repulsion (@ lone pair bond pair > bond pair -bond pair > lone pair (@)_ increasing p-orbital character in sp? lone pai 23, Which on ofthe following pairs of species have the same Inwhich of the following speciesthe interstomicbondangle bond order? is 109928"? (@ CNandNot (6) Cand CNY @) NH, BP; (©) NH,.BF, (© O;amaCN- ———(@)_NOtand CN ©. NH Bry @ NH. BR, 24, Ny and 0, are converted into monocations, Nf and In XeF,, XeF and XeFy the number of lone prs on Xe are respectively Of respectively. Which ofthe following statements is @ 231 ©) 1.23 ae © 412 @ 321 Hybridisation of the underline atom changes in: @ In Nj,N-Neond weakens (@) Allchanges to Aig (©) In 0§, the O- Obond order increases 0 oer (© in O$. paramagnetism decreases (© Nf becomes diamagnetic 5.@OQO@ 6.@OOO 17.@O0OO 18.@OQO@ VY. @O0OO@ 20.@@QO@O_1.©@OOO_2OOOO_3.@OO@_¥4. @OOO ‘Space for Rough Work 1o-16_ -————________________—_ DPP/ CC04 25. The bond dissociation energy of B ~ F in BF, is (646 kJ mot whereasthat of C—F in CF is 515 J mot“, The correct reason for higher B ~ F bond dissociation energy as compared to that of C- Fis, (@) stronger 6 bond between B and Fin BF, as compared tothat between Cand Fin CF (&)_ significant pr printeraction between B and Fin BF, whereas there is no possibility of such interaction between Cand Fin CF, (© lower degree of px—pr interaction between Band Fin BF, than that between C and Fin CF, (smaller size of B-atomas compared t that of C-atom. 26. Ortho-Nitrophenol is les soluble in water than p- and m- Nitrophenols because (@)_o-Nitrophenol is more volatile steam than those of m- and peisomers. (©) o-Nitrophenol shows intramolecular H-bonding (©) o-Nitrophenol shows intermolecular H-bonding (@)_ Melting point of o-Nitrophenol is lower than those of ‘me and p-isomers 2. 2. Amongst LiCl, RECI, BeCl, and MgCl, the compounds with the greatest and the leat ionic character, respectively are: (@) LiClandRbct () RbCland BeCl, (©) MgCl, andBeCl, —_(@) RbCland MgC, Bond order normally gives idea of stability of a molecular species. All the molecules viz. H, Lip and B, have the same bond order yet they are not equally stable. Their stability order is (@) Hy>By>Li, ©) Li>H>B, (© Li>By>H, @ By>H,>Li, ‘The shape of IF; is (2) Trigonally distorted octahedron (©) Pyramidal (©) Octahedral (@) Square antiprism ). Which one ofthe following molecules is paramagnetic? @ Ny ) NO © co @ 05 23@QO@O %@OO@ 30.©@0OO 21.@OQO@ BOOOO@ 2%. @OO@ AILY PRACTICE BLEM DPP CHAPTERWISE EMISTRY Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 35 Qualifying Score 50 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End Time : CHEMISTRY (Ccos SYLLABUS : States of Matter Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Daly Practice Problem Sheet contains 30 MCQ's, For each question only one option is correct Darken the correct cicle/ bubble in the Response Grid provided on each page, Which ofthe following volume (V) - temperature (T) plots represents the behaviour of one mole of an ideal gas at one atmospheric pressure ? vo G08 vw. vw 2a 52K) G06 ora) 2a sk) ean 73K) a0) oo @ = = o™ o™ 1. @©O@ ‘Space for Rough Work 1e-18 -————_—______________——— DPP/ CC 05 2 2 ‘The volume-temperature graphs ofa given mass ofan ideal ‘gas at constant pressure are shown below. ere} 7™— ‘What isthe correct order of pressures? @ py>73>P2 ©) py>P2>Ps © P2>P5>P, (@® P:>P,>Ps ‘Theinversion temperature 7;(K) ofhydrogen i (given van det Waal's constants a and b are 0.244 atm L? mol? and (0.027 L mot respectively) @ 40 © 2% © 10 @ w ‘Thetemperatue ofthe gasis raised from 27°C t0 927°C, the root mean square velocity is (a) JO27727 time the earlier value () same as before (©) halved @ doubled ‘Equal masses of methane and oxygen are mixed in an empty container at 25°C. The fraction of the total pressure exerted by oxygen is @ 2 © 23 1273 @ 1.23 @) 18. eo 7S @ ‘Theratio between the root mean square speed of H, at 50K ‘and that of, at 800 K is, @ 4 © 2 © 1 @ V4 Calculate the total pressure in a 10.0 Leylinder which contains 4g helium, 1.6 goxygen and 1.4 gnitrogen at 27°C. 9% 10. a. @ 04924 © 492m © 452am @ 00892am A bottle of dry ammonia and a bottle of dry hydrogen chloride connected through a long tube are opened simultaneously at both ends the white ammonium chloride fing frst formed will be (@) at the centre of the tube (b) near the hydrogen chloride bot. (©) near the ammonia bot. (@ throughout the length ofthe tube. ‘The rms velocity of CO, at temperature T (in kelvin) is x arms, At what temperature (in kelvin) therm, velocity ‘of nitrous oxide would be 4x ems"! @ 16T ) 27 © 4T @ 2T Armixtute of two gases A and Bin the mole ratio: 3is kept ina 2litre vessel. A second 3L. vessel has the same two gases inthe mole ratio 3:5, Both gas mixtures have the same tem= perature and same foal pressure. They are allowed tointer- ‘mix and the final temperature and the total pressure are the same as the inital values, the final volume being 5 litres. Given that the molar masses are My and Mg, What is the ‘mean molar mass ofthe final mixture? 5M4+8My TIM, +123M 5 @ © om ( Mas (@ 2MasTMy 250, 150 Atconstant volume and temperature conditions, the rate of diffusion D, and Dp of gases A and B having densities pg, and pg are related by the expression. 2 w2 @) >,=[D24] ) Depa B Pa (@ Dy=o( 28) an 2 @OO@ 3 @OO@ 4 OOO 5. @OO@ 6 OOOO 7. @OO@_8 @OO@_9 ©OO@ 1.@@O@_U. @OO@ ‘Space for Rough Work GP_3371 DPP/ CCO$ ttt 2 2B. 4 15, 16. For one mole of a van der Waals gas when b = 0 and = 300K, the PV vs, I/V plots shown below The valve ofthe iis @ 10 © “Asthe temperature i raised from 20°C to 40°C, the average kinetic energy of neon atoms changes by a factor of which of the following ? 45 © 15 @ 30 @ 313/293 © {GI37295 © 12 @2 “Maximum deviation from ideal gs is expected from @ N@ ©) Cy) © Ni@ @ Hye) Equal masses of H,,O, and methane ave been taken in a container of volume ¥ at temperature 27°C in identical conditions. The ratio ofthe volumes of gases Hy : Oy : methane would be: ° @ 8:16:1 () 16:8:1 TU 18. 19. ‘Which one ofthe following statements is NOT true about the effect of an increase in temperature on the distribution ‘of molecular speeds in a gos? (@)Thearea under the distibtion curve en asunder the lower temperature ‘The distribution becomes broader ‘The faction ofthe molecules with the most probable speed increases (@) The most probable speed increases ‘According to the kinetic theory of gases, in an ideal ga, between two successive collisions a gas molecule travels (@ ina wavy path (©) inastraight ine path (©) withan accelerated velocity (@ inacircular path For { mol of an ideal gas at constant temperature 7, the plot of log P) against (log V)isa(P: Pressure, V: Volume) (@) Straightline parallel tox-axis ©) Straightline witha negative slope. (© Curvestarting at origi. (0) Straight ine passing through origin. ‘When CO,(g) is passed over red hot coke it partially gets reduced 10 CO() Upon passing 0.5 Lot CO,( over red hhotcok, the total volume ofthe gases increased 0 700m. ‘The composition ofthe gaseous mixture at STPis ns the same o © 21, For gaseous state, if most probable speed is denoted by C*, One Ons Led average G and mean square speed by C, then for Equal moles of hydrogen and oxygen gases are placed in a ge speed by C Sauare sped by C. ‘container with a pin-hole through which both can escape. acl emule Of mcheciles tne ration Ol iene se ate ‘What fraction ofthe oxygen escapes in the time required for = (@)_C*: G +C=1.225;1.128:1 ‘one-half of the hydrogen to escape ? () C¥: C= 1.128:1.225:1 @ 1” ©) 14 (©) C#:G:C=1:1.128:1.225 © ® @ 12 (© CHG C=1:1225:1.128 2.@OQO@ B@OOO 4.@OOO 4.@OO@ 16. @©OO@ 17.@©QO@_B.@©OQOO_.©@OOO_2.@OO@_4. ©©OO@ ‘Space for Rough Work 1620-—$— i i —. DPR C05 22, Sulphur dioxide and oxygen wer allowed to diffse through 8 porous partition. 20 dm® of SO, diffuses through the porous partition in 60 seconds. The volume of in dn? ‘which diffuses under th similar condition in 30 seconds will be (atomic mass of sulphur = 32 @ 1 © MI © 100 @ 22 23, Byhow many folds the temperature ofa gas would increase ‘when the rot mean square velocity ofthe gas molecules in ‘container of fixed volume sinerease from 5 < 10¥emsto 10x 10%emis? (@ Two () Three © & (@) Four 24, The temperature at which oxygen molecules have the same ‘oot mean square speed as helium atoms have at 300 K is: Atomic masses: He=4.u,0= 16) (@ 30K &) GOK (© 120K, (@ 200K 25. 1fZ.is.a compressibility factor, van der Waals equation at low pressure can be written as: @ Z Zot o o vat Pb © z zeit © @ Fa 26. ‘The intial volume of a gas cylinder is 750.0 mL. If the pressure of gas inside the cylinder changes from 840.0 mm, Hg to 360.0 mm Hg. the final volume the gas willbe: @ 1750L () 300L, © 40x @ 7501. 27, 56g of nitrogen and 96 g of oxygen are mixed isothermally and ata total pressure of 10 atm, The partial pressures of ‘oxygen and nitrogen (in atm) are respectively oes ©) 55 © 28 @ 64 28, Two vessels containing gases A and B are interconected as shown in the figure. The stopper is opened, the gases are allowed to mix homogeneously. The partial pressures of A ‘and Bin the mixture will be, respectively Gas GB m1 SL (@) Sand aiom (&) Sand 4atm (©) 48and2atm @ 64and4atm 29. Anneon-dioxygen mixture contains 70.6 g O, and 167.5 g neon If pressure ofthe mixture of gasesin the cylinder is 25 bar. Whats the partial pressure of O, and Ne in the mixture respectively ? (@) 5.25bar, 10tar (b) 19.75bar,5.25bar (©) 197Sbar,1Obar —d)_‘5.7Sbar, 19-75 bar 30, Letthe most probable velocity ofhydrogen molecules at a temperature of ®C be Vp. When the temperature is raised to (2t + 273)°C the new tms velocity is (suppose all the molecules dissociate into atoms at later temperature) @ 2, ov o Kn a ee News | is 2.@0@Q@ 23.@@O@ 21.©OO@_B.@O0O@ A@OO@ 3@QOOQ@ %. OOOO 29.@OO@ _30.@OO@ DAILY PRACTICE PROBLEM DPP CHAPTERWISE 5 - CHEMISTRY Total Questions Total Marks Attempted Correct Incorrect Cut-off Score 38 Net Score Qualifying Score Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Start Time : End CHEMISTRY (ccoe ‘SYLLABUS : Thermodynamics Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1, Assuming that water vapour is an ideal gas, the internal energy change (AU) when I mol of water is vapourised at 1 bar pressure and 100°C, (given : molar enthalpy of vapourisation of water at I bar and 373K =41 KI mol and, R=83Jmol! K"} willbe (@)_ 41.001mor () 4.100khmor* (©) 37904 mor (@ 379041 mot 2 In-aclosed insulated container, a liquid is stirred with a ppadale to increase the temperature, which ofthe following is true? (@) AE=W20,9=0 (© AB=0,W=970 () AB=W=940 @ W=0,AE=420 3 ‘The maximum work which a system can perform at constant temperature and pressure equals (@) AH-AE @) CAG) © q-AE @ PAV-aG ‘The entropy change in the fusion of one mole of a solid melting at 27°C (Latent heat of fusion, 2930 I mol) (@) 9.773 mot ©) 10.735"! mot! (©) 29305! mol! (@ 10853K"! mol! men 41. ©QOOO_ 2 @OOO_3 @©O0OO_4 OOOO ‘Space for Rough Work 1622- —$< ——. DPR C08 s. 2 % ‘The enthalpy of vapourisation of water from the following, two equations is Hy@)+3029—> H,0 (1), AH=~286K0 245.5kI Hz (2) +402 (@)> H20 (A @ sow &) 4050 © @30 @ 1258 ‘The standard enthalpy of formation of NH, is -46,01I mob If the enthalpy of formation of H, from its atoms is = 436 kU mol"! and that ofN is -712 kJ mol! the average bond enthalpy of N~H bond in NH, is (a) -964kI mort (b) +352KImor"! (©) +1056K mot"! (@ -1102kI mor" Calculate enthalpy change for the change 85(—)43@S4(e), given that H,S3(g) —92H(g) +25(),AH = 239.0 kealmot™! H,S(@)—2H(g) +8(g), AH =175.0kcalmot! @ +5120keal (©) -5120keal © S080keal (@ ~5080keal From the following bond energies H—Hond energy: 431.37 KI mot! C= Cond energy: 606.10 mot! (C-Cond energy: 336.49 kJ mot! (C—Hbond energy: 410.50 KI mol? Enthalpy for the reaction, HH HH HH HH willbe: (@) -2436kImol" —(b) 120.055 mot! (©) 5530kmor! —@) 15236kI mot" ‘On the basis of the following thermochemical data : [SHAH =01 10. a 2 1B. 4 H0() +H" (ag) + OH (ag); AH = 57.324 stg) 8000; e282 ‘eval cena mation oH ona 28°C (a) -22888kI (b) +228.88kI_ 6 sau @ “zai Teraprl eecin npr, ad Selvinmdlo cba ne Wee angen sruium eesti wb one he @ nor Onn © tusimr ree Conte awn senate eon 2CgHjg(g) +25 02 (8) + 16C02(g) +18H20(s) Thesgnt a8 yee OS Cee Bie Bon {hea conn pn on ae (a) TAS> AH, AH (b) TAS > AH, AH: OS asaat a (TASH a ye, as tye, AS: -ve, AS: ye, AS: ‘The enthalpies ofthe following reactions are shown below. L 1 Hae) + 70x) OH) AH =42.09 kd mol! ‘Ha(g) > 2H(g); AH = 435.89 kJ mol-! 0;() 206) + AH=495.051 molt Calculate the O — H bond energy for the hydroxy aia @ BB18KImor! ) 42B38KI mor (©, 51328KImol!—@)11338KI nok When lites ofa gas mixture of methane and propane is perfectly combusted at OC and 1 atmosphere, 16 lite Of oxygen at the same temperature and pressure is consumed. The amount of heat released. from this combustion in KI (AHLag, (CH) = 890 KF mol, AH ap (CyH)= 22201 mols @ 2 &) © 37 om 1.®@@QO@O_U.@OO@ 5. @©OOO 6 @QO© 7. @OO@ & OOOO % OOOO 12.©©©@ 13.@©O@_14. @OOO ‘Space for Rough Work GP_3371 DPP/ CC06 — ——_ tics 15, 16. a. 18, 1. The heat of combustion of carbon to CO; is 393.5 kl/mol. The heat released upon formation of 35.2 g of | (@) 250K © -125K0 ©) +125K (a) +250K0 CO, from carbon and oxygen gas is 21, Standard entropy of X,, Y, and XY, are 60, 40 and @) -315KI (b) +315KI 50K“! mol", respectively. For the reaction, © -60K @ 3158 1d ‘Using the data provided, calculate the multiple bond energy “2+ 7 ¥2 > XYs-AH= -S30Kt tobeat equilibrium, the (GJ mol") of aC= C bond in C,H, That energyis (take the temperature will be bond energy of a C ~H bond as 350 kJ mol!) (a) 1250K (b) 500K 2C{s) + Hyg) —> HC=CHig), AH=2251d mol"! (© 10K (@ 100K 20%) —> 2049); aH1= 141010 mor! 22, Theenthalpy changes fr the following processes are listed H,(@) —> 2H); AH=330K mot! below 1 oan Oo C1@)>20K6), basis! aaa Och 1@)21@), 's1.0.smer"! TCle)>16g)+ C1, 2113 mot Fora givenreacton, AH=3551Umol! andas=8363K! (0 1 eee nmol Thereactionissponaneousat:(Assomethat Hand HOD? TRIN es ven thatthe standard states for iodine and chlorine are oa 1@)and Cp he standard ofan oI) (©) T>298K (@) T<425K o YI (@) 68kI mot IFan endothermic rection is non-spontancous at freezing 7 (©) 4248kImot tof water and becomes feasible ait boiling pont, then se (© -146KIm0r" (@) AH is-ve, as istve @ -1681) mot () AH and As both are Wve 23, Bond enthalpies of H, X» and HX arein the ratio2: 1:2. © AH and As both are-ve enthalpy of formation of HX is — 50 KI mo the bond (© ad is He, as is-ve enthalpy of Xs ‘The standard enthalpies of formation of CO,(g), H,0() and (@) 100kI mot"! (©) 300K mot lucoses) at 25°C are~400 k/mol,-300kVmoland=1300 —(¢) 2001 mot! (@ 400K mot! {/mol respectively. The standard enthalpy of combustion 24, Given that per gram of glucose at 25°C is . @ 29008 @) -2000K © dsH°of N20 is 82kI mot! (© —I6i1K @ Hen (@_ Bondenergies of N = N,N=N,O=OandN =O are Ifa 298K thebond energies ofC—H,C—C,C=CandH 946,418, 498and 607 kl mot respectively, —Honds are respectively 414, 47, 615and435kI mol", The resonance energy of NO is, the vale of enthalpy change forthe reaction @ -38 ©) ~603 H,C = CH, (g)+H3(g) > HxC—CH,(g) at 298K (© 620 @ 40 willbe SI F.OOOO 16.OOOO 17.OO0OO BOOOO V.OOOO uD 20.@@QO@ _21.©@OO@ 2.@©OO_23.@OO@_ 4. @OOO ‘Space for Rough Work 25. Given that bond energies of H- Hand Cl ~Cl are 4301 mol! ‘and 240 KS mol“! respectively and AH, for HCI is ~ 90 KI mot-!, bond enthalpy of HCIis, (@) 380k mot! () 425k mot! (©) 245k mot! (@ 290K mor! 5. Under isothermal condition for one mole of ideal gas what is the ratio of work done under reversible to irreversible process intially held at 20 atm undergoes expansion from ILto 21, at 298K, under external pressure of 10 tm? @ 17 ) 20 © 14 @ 10 . Temperature ofS moles ofa gasis decreased by 2K at constant pressure. Indicate the correct statement () Work done by gas is= 5 R (6) Work done over the gas is= 10. (©) Work done by the gas = 10R 30. (@) Work done=0 . For complete combustion of ethanol, CHIsOH( 1) +303 (s) 42002 (8) +3H0(0) the amount of heat produced as measured in bomb ‘calorimeter, is 1364.47 kJ mol-! at 25°C. Assuming ideality the enthalpy of combustion, AH, forthe reaction wil be: (R=8314K0 mot!) (@) 1366951 mot" © 1460.95 ks mor! (b) -1361.95 ky mor (@ ~1350.50k mor" 1626- $< —. DPP/ C08 29, Read the following statements carefully and choose the @ Expansion of a gas in vacuum (p., = 0) is called free expansion, i) Work is done during free expansion of an ideal gas whether the process is reversible or irreversible Gi Nowork is done during free expansion ofan ideal gas whether the process is reversible or irreversible (Gs). Nowork is done during free expansion ofan ideal gas when the process is reversible @) Only statement (ii) is correct ()_ Statements () and (ii) arecomect (©) Statements (i) and (iv) are correct (@ Statements (i) and (v) are correct ‘The (S*) ofthe following substances are: (CH, (@) 186.25K-! mot! 04 (g) 2052JK-! mor! €0, (g)213.65K"! mot H,0(@)69.9.K"! mor! ‘The entropy change (AS*) forthe reaction CHG) + 2048) > COs) +2H,Ois: (@) -31253K molt (©) ~24285K" mol (©) ~108.1K mol @ -3763K"' mot 30.©©O@ 3.@OO@ %OOOO 27.©O©OO BOOOO %. OOOO GP_3371 AILY PRACTICE PROBLEM DPP CHAPTERWISE Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 36 Qualifying Score 52 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End CHEMISTRY ([cco7 SYLLABUS : Equilibrium Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. K, forthe reaction Np (@)+0)(g) = 2NO@) 81300 K is 4.0 10-6, K, for the above reaction willbe (R=2eal mot! KF) (@) 24%103 @) 4x10 © 410° RTE @ 16x10? 2. AL1O0°C the, of water is 55 times its value at 25°C. What will be the pH of neutral solution? (log 55 = 1.74) @) 613 () 7.00 © 781 @ 513 3. Thedissociation constant ofa weak acids 1x 10-4. In order to prepare a buffer solution with a pH = 5 the [SaltJ/[Acid] ratio should be @ 1:10 © 4:5 © wr @ 84 ‘The exothermic formation of CIF, is represented by the equation: Ch(g)+3K(@) 220Fy@); AH =-32910 Which of the following wil inerease the quantity of CI, in amequlitrium mixture of C.F, and IF? (@) Adding Fy (©) Increasing the volume ofthe container (©) Removing Cl, (@) Tncreasing the temperature 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work 10-26 ——____________________——— DPP/ CC07 5. The Ky of Ag,CrO,,AgCl, AgBr and Agl are respectively, 9, Lt TO"2, 138% 10-1, 510 x 1073, 8.3 « 10-1, Which cone of the following salts will precipitate lst if AgNO, solution is added tothe solution containing equal moles of NaCl, NaBr, Nal and Na,CrO,? (@) AgCl () Agbr (©) Ag,CrO, @ Agl 6 MY andNY,, twonearly insoluble salts, have the same K,, values of 6.2% 10-! at room temperature, Which statement ‘would be true in regard toMY and NY, ? (@) The molar solubilities of MY and NY, in water are identical. (©) Themolar solubility of MY in wateris lessthan thatof 10. NY, (©) The salts MY and NY, are more soluble in 0.5 M KY than in pure wate. (The addition ofthe sat of KY to solution of MY and NY, will haveno effect on their solubilities 17. The following reaction i performed a 298 K. 2NO{g) +0518) = 2NO,(®) ‘The standard free energy of formation of NO(g) is 86.6 kj/mol ‘298 K. What is the standard free energy of formation of NO,(g) 31298 K?(K, = 6x 10"2) In (1.6 x10") @ 86600- “R298 (b) 052 86,600-R(298)In(.6 10)) (©) R298) In(1.6 10!) 86600 (@), 86600 + R98) In(1.6 102) 8. Consider the following liquid - vapour equilibrium, Liquid = Vapour Which ofthe following relations is correct ? dinG _ AH, afnP _ Ally 2 a ee © T,, the ‘yield of ammonia asa function of time is represented by @ © © @ 10.©©O@ 5. @©O@ 6 @OOO 7. ©O©O@ 8 OOOO % OOOO ‘Space for Rough Work GP_3371 DPP/ CCo? —— iii nL. 2 B. 4 18. ‘Concentration of the Ag* ions in a saturated solution of AQsC;0, is 2.2 « 104 mol Ll. Solubility product of ‘Ag;C,04i8 = @) 266 10-2 () 435x101 © 53x10 @ 242x104 16. @) 63am ©) 69320 © 63am @) 0.693aum ‘The first and second dissociation constants of an acid HA. are 1.0 x 10° and 5.0 x 10-1? respectively. The overall dissociation constant of the acid will be For the following reaction in gaseous phase Ci eyes CO(G) + 5.0368) COR) Ky K is © 50x:10!5 @ 50x10, fix io @ «en? © ey? 17, 2.5m of 2/5) M weak monaaciicbase Ky, =1 10-12 ° er 25?) is tivated with (2/15) M HCL in watet at 25°C. The © me « ‘concentration of H* at equivalence point is (K,,= 1x 10 ‘The degree of dissociation of PCIg(a) obeying the at25*C) ‘equilibrium PCls = PCI; +Clp isrelated tothe equilibrium @ 37x104M ) 32x107M pressure by © 3.2x10?M (@) 2.7x102M 1 18, Calculatethe pH of solution obtained by diluting I mL.of| @ act &) ax 0.10 M weak monoacidic base to 100 mL at constant rt temperature if Ky of the base is 1 x 10-5? © act @ aeP @ 8 9 P © 0 @u ee eee Soeaer Cos) =p prom " 19. Ina saturated solution of the sparingly soluble strong ‘The volume of the container is now decreased by moving lecralyte AgIO, (molecular mass = 283) the equilibrium the movable piston fitted in the container, The maximum which sets is AgIO5(3) ——= Ag*(ag)+105 (ag). Ifthe volume ofthe container, when pressure of CO, attains its solubility product constant Ky of AgIO at a given ‘maximum vale, willbe = temperature is 1.0 x 10°, what is the mass of AgIOS, (Given that : SrCO, (8) = S10 (s) + CO,(g), Kp= 1.6atm) a ® Ole @) Atie @ 10x104g () 283x102, (©) 2litre @) Slitre (©) 283x105 @ 10x1078. For the reaction Cy + CO) ->2COigy Kp =63atm at 1000 20. Species acting as both Bronsted acid and base is K. tf atequilibriam: Peo 10 Peo, hen'he total pressure (@)_(HSO" () NaC0, ofthe gases at equilibrium is © ™, ator 1.@Q@O@ L.@©OQOOO B@OOO H4.@OO@ 1. @OOO@ 16.@O©@O@_17.@OQOO_¥B.@OOO_Y.@OO@_20. ©©OO@ ‘Space for Rough Work 1628 -——_____________________—————- DPP/ CC07 21. Let the solubility of an aqueous solution of Mg(OH), be x then its K,, is @ 4c @) oR © me @ 9. 22, The Ky for COW, is 1.6 x 10, The solubility of this ccompotind in water is @ fea ©) Vex 27 @ Vie © 16x10" 23, Which equilibrium can be described as an acid-base reaction using the Lewis acid-base definition but not using the Bronsted-Lowry definition? (@)_2NH, +H,S0, = 2NH," +S02- (©) NH +CH,COOH = NH," +CH,COO- (©) H,0+CH,COOH = 1,0" +CH,COO- (@ (Cultt,0),?-+4NH, = [Cu(NH) 7 +4H,0 24, Which one ofthe following statements is not true? (@)_ pl + pOH= 14 for al aqueous solutions () ThepHofl x10 MHClis8 ©) 96,500 coulombs of electricity when passed through a CuSO, solution deposits 1 gram equivalent of copper at the cathode (@) The conjugate base of HPO; is HPO 25. How many ites of water mustbe added to 1 tre an aqueous solution of CI with a pH of I tocreate an aqueous solution with pH of 2? (@ OIL) 09L 26. Forthereacton 2NOgle) —* 2NOKE) + 028), (© 20L @ 90L (K, = 1.8 x 10° at 184°C) (R= 0.0831 k/ (mol. K)) When Ky, and K, are compared at 184°C, itis found that (@) Whether K, is greater than, less than or equal to K, depends upon the total gas pressure ©) K=K, (©) K, istess than K, (@ XK, is greater than K, 27. Zitconium phosphate (Z:,(PO,),] dissociates into three ‘irconium cations of charge +4 and four phosphate anions of charge 3. Imola solubility of zirconium phosphate s denoted by S and its solubility product by Ks then which ofthe following relationship between S and Key is correct?” (@) S=(K,/(6912!7)() S=(Ky/ 144}! © S=(K,/6912)!7_— @)_S={K 6912)" 28 The pK, ofa weak acid, HA is 480. The pK, ofa weak bas, BOH, is 4.78. The pH of an aqueous Solution of the correspondng salt, BA willbe @ 958 © 49 © 701 @ 92 29. Which one ofthe following arrangements represents the correct order of solubilities of sparingly soluble sats Hg,Cl,, Cr(S0,);,BaSO, and CrCl respectively ? (@) BaSO, > HexCly > Cry($04)3 > CrCl, (©) Ba80, > He,Cly > CrCl > Cy(SO4), (©) Ba8O, > CrCl, > Hg3Ch > Ca (S04), (@_Hg,Cly > BaSO, > CrCl; > Cr (80,)s 30. Calculate the pH of 0.5 M aqueous solution of NaCN, the pK, of CN~ is 4.70 @ 470 o7 @ us @ 65 21.@©O@ 2@OO@ 2%.@OO@ 27.©@0OO Resroxse Grip B.@OOO 4.©@OOO 25. @OOO B@OOO Y@©O0OOO W. @OOO Total Questions Attempted DAILY PRACTICE PROBLEM DPP CHAPTERWISE 7 - CHEMISTRY Total Marks Incorrect Cut-off Score Correct Net Score Qualifying Score 50 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End CHEMISTRY (ccos ‘SYLLABUS : Redox Reaction Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. Inwich ofthe following pairs, here is greatest iferencein Several locks of magnesium are Fixed to the botiom of a theoridaton number ofthe underined elements? ship (@) NO; and NO, () Py 0s and PO (@)_ make he ship lighter ee! oR {© prevent eta of water ad sak © N,0 and NO (@) SO, and SO, (©) prevent puncturing by under-sea rocks {@) Keepaway te sharks (@) NaCl+KNO, NaNO, +KCI 4. When KMnO, reacts with acidified FeSO, : (@) FeSO, is oxidised and KMnO, is reduced (b) CaCO, +2HC1 CaCl, + H,C,0, (only KM, soxiised (©) Mg(OH), + 2NH,CI — MgCl, + 2NH,OH © nly FeSO, boxed @) Zn 2AG0N ~> 28g +71CN)y (@) None ofthese 2. Which of the following is a redox reaction? 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work {e390 ppP/ CC08 58. 9. Which of the following chemical reactions depict the ‘oxidizing beahviour of ,SO,? (@) NaCl + H,S04—> NaHiSO 4 + HCL ©) 2PCIs +1150, —> 2POCI, +2HC1+S0,C1, © 21 +H,804— 1p +807 +240 (@) Ca(OH), + HO, —> CaSO, +2130 Which of the following statements are correct concerning redox properties? @ A metal M for which E° for the half life reaction MP + ne == Mis very negative wll be a good reducing agent. Gi) The oxidizing power ofthe halogens decreases from chlorine iodine Gi) The reducing power of hydrogen halides increases from hydrogen chloride to hydrogen iodide © @.civandiy ©) @anddi © (only @) Gi)and Git) Inthe following balanced reaction, XMn0j +¥ C03 +ZH" 2 == Mn +270) +5420 values of X, Yand Zrespectively are @) 25,16 ) 8, © 5,216 @ 5,84 ‘Arrange the following in the order of their decreasing electrode potentials: Mg, K, Ba and Ca SR CouaK em otuiscerel (©) CaMg,K.Ba (@) Mg,Ca, Ba,K Given XNa,HAsO, + YNaBrO, + ZHCI > [NaBr + HyAsO, + NaCl 2 1B. M4 ‘The values of X, Y and Z in the above redox reaction are respectively @ 212 © 213 © a16 @ 314 Oxidation state of suiphur in anions $O3°, $,03° and '$,02° increases inthe orders. @ 8,0} <8,0} 208° 7H0 + 3NP* a @ HO oN (©) 1,80, is the reducing agent because it undergoes eae ow @ G,0F (@ HO, isthe reducing agent because it undergoes 23. Which of the folowing reactions depict the oxidising reduction behaviour of H,S0, 17. The species hat undergoes disproporionaioninan alkaline @)2pCIg +4%,S0y—>_ 2POCy +2HC1+03C, medium are @ a © Mnof- (©) 2NOH + H,80, —+Na,S0,+H,0 (©) NO, (@) All of these (©) NaCl +H SO, —+NaHSO, + HCI 18. How many electrons are involved in the following redox ena (© 216 H,80, —r1, +80, +241,0 cos es $0} 3c?" Fe" c0, Ua) 24 Which oe of the folowing resco involves @ 3 @ 4 (@) 2H,S0, +Cu—> CuSO, +2H,0+S0, © 6 @ 5 A805 34,5 —»As,S, + 3H,0 19, HSactsonlyasareducing agen vhileSO,canact bothas ——@)_ KOHL G29 KCL ROCA 0 ‘Teducing and oxidizing agent because {@) CaP, 68,0» 3Ca(OH), 27H, 5.@OQO@ 6.@OOO 17.@O0OO 18.@OQO@ VY. @O0OO@ 20.@@O@_21.©@OO@ 2.@©OO_23.@OOO@_¥%4. @OOO ‘Space for Rough Work fe ppP/ C08 25. Point out the correct statement of the following about Na,SO, (a) Average oxidation numberof $ atom is +2 (©) Oxidation number of two S atoms is zero each and that of other two is +5 each (©) Oxidation number of twoS atoms is+1 each and that of| other two is-+4 each (@) None of these 26. ‘The pair of compounds in which both the metals are in the highest possible oxidation state is (@) [Fe(CN)g1* [CCC ©) Cx0,Cl, MnO (©, Ti0s, MnO, @ [Co(CN)g]*, M03 27. Thicsulphate reacts itferently with iodine and bromine in the reactions given below. 25,0} +1, -»8,02° +2" 8,0} +2Br +5H,0-» 250} +2Br- +1081" ‘Which of the following statements justifies the above dual tehaviour of thiosulphate? (@) Bromineisa stronger oxidant than iodine (6) Bromine is weaker oxidant than iodine 28. 2. (©) Thiosulphate undergoes oxidation by bromine and reduction by iodine in these reactions (@ Bromine undergoes oxidation and iodine undergoes reduction in these reactio ‘Standard reduction potentials of the half reactions are given below: Fy(g) +269 2F-(aqy Lye) +26 > 2C1(aq); E° Br,() +26 2Br (aq) 1,6) +26 2F-(ag) The strongest oxidi (@ Fant () Br, and © Chand Br (@) Chand, A mixture of potassium chlorate, oxalic acid and sulphuric acid is heated. During the reaction which element undergoes ‘maximum change n the oxidation number ? @ s @ H © cl @c ng and reducing agents respectively ). Zn gives H, gas with H,SO, and HCI but not with HNO, because (@) Znactsasan oxidising agent when itreacts with HNO, (©) HNO, is weaker acid than HSO, and HCL (©) Inelectrochemical series, Zn is above hydrogen (© NO; is reduced in preference to hydronium ion 3#0.@0O@ 3.@OQOO WOOOO 27.©OOO B@OOOO %. OOOO TANT ase AON eos @)>] NOP ee alas UN cee Ld Total Questions Total Marks Attempted Correct Incorrect Cut-off Score 40 Net Score Qualifying Score Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End Time : CHEMISTRY (Cco9 SYLLABUS : Hydrogen Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. Which ofthe following will not displace hydrogen 3. The adsorption of hydrogen by metals i called @ B (@) Dehydrogenation (b) Pb (0) Hydrogenation © He (©) Occlusion: @ Sn (@)_ Adsorption 2. Which statement is correct for hydrogen ? 4. The low density af ice compared to water is due to, (@ Tehas avery high ionisation potential (@) hydrogen bonding interactions () tis always collected at cathode (©) dipole dipole interactions (©) Itcan exists both in +1 as well as —1 oxidation state (©) dipole — induced dipole interactions (d)_ It has same electronegativity as halogens (@) induced dipole ~ induced dipole interactions 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work fe, ——_—_—_—_—_——_________ pP/ CC09 5 1 9% Which ofthe following terms is not correct for hydrogen ? @Ismolecul is dstomie (b) It exists both as Hand H- indifferent chemical compounds (© tis the only species which has no neutrons in the nucleus (© Heavy water is unstable because hydrogen is substituted by its isotope deuterium Hydrogen canbe fused to form helium at (@) High temperature and high pressure (©) High temperature and low pressure (©) Lowtemperature and high pressure (@) Lowtemperature and low pressure ‘The hydride on, i stronger base than the hydroxide ion, OFF. Which one ofthe following reactions will occur if sodium hydride (NaH) is dissolved in water? (@H°(@g)+H,0(0 + H,0°(aa) ©) Haq) + ,0(0 > OF (a4) + Ha(8) (© 1 (aq)+H,0(0) > OH (ag) +24" (aq) +20 (@ _H(aq)+H,0(0 No reaction Blackened ol painting can be restored into original form by the action of (@ Chlorine () Bad, © 10, @ Mn0, Which of the following reactions is an example of use of ‘water gas in the synthesis of other compounds? mK (@) CH, (2)+ H,0(2) 3+ CO(2) + Hp (2) (©) CO(g)+H,0(e) S5S>CO> (2) + Ha (z) © CyHags28H0(@)—2™® 5 nC0-+(2n-+1)Ha (© CO(g)+2Ha(s) See CH OH) 10. Elementsof which ofthe following groups) of periatictuble do not form hydrides? Groups, 8,9 (6) Group 13 © Growps15.16,17 —(@) Group id 11. Which one ofthe following pairs of substances will not produce hydrogen when reacted together? (@) Copper and conc nitric acid (©) Ethanol and metallic sodium (© Magnesium and steam (©) Phenol and metalic soium 12. Which of the following is not a use of dihydrogen ? (©) eased in fuel cells for generating electrical energy. (©) Atomic hydrogen and oxy-hydrogen torches are used for cutting and welding purposes. (©) Teused in the synthesis of hydroquinone and tartaric sid (© Both (b) and (e) 13, Calculate the normality of 10 volume H,0,? @ 17N © BN (@ 303N @ 0.0303N 14, _Acits melting point iceis lighter than water because (@)_ H,O molecules are more closely packed in solid state (©) ice crystals have hollowhexagonal arrangement of HO molecules. (©) onmelting ofice the HO molecule shrinksin size (@ ice froms mostly heavy water on fist melting. 5. @0OO@ 6 @OO@ 1.@@QO@_U.@OO@ 7. @0O@ §& @O0OOO % Q0O@ 12.@@O@_13.©@OOO_14. @OOO ‘Space for Rough Work GP_3371 DPP/ CCO9 —_$ A i tt 18. 16. aw. 18, w. Identify x and y in following reaction: 20, Hydrogen molecules differs from chlorine molecule i the 7 electrolysis nycrolysis following respect PESO Coa * (@)Hydeogen molecule is non-polar but chlorine molecule y+ 2H%ag) + H,O,f09) an 'e (@)_x= H,SO, (aq), y = 2HSO4(aq) (@) Hydrogen molecule is polar while chlorine molecule is () ¥=HO,$0080;1aq), » = 2405 aa) non-polar (© x= HO,SOOSOsH (aq), y = H,S0,(a9) (©, Rydoge mesa farm inermoeariopn (@_x=H,S0jaq) , y= HO,S00S0;Hlaa) Ss but chlorine molecule dows Which of the following species is diamagnetic in nature? @ aaa ee in coordination @ HD ©) HY 21, Which of the following chemicals is not present in clear © @ tes hard water? (@) Mg0O, (b) Mgso, ‘The number of moles of H, in 0.224 litre ofhydrogen gos a ‘atSTP(273K, 1 atm)is: © MgtHCo;), @ GC, @ a 22, Trueperoxideis ©) 01 @ Bx) () MnO, fa ae (© Po) (No, Hydrogen is not obtained when Zn react with 35. Vey pare drogen (99:9) can be mae by which of the (a) cold water S) Renttoat methane with pana (@) Reaction of methane with steam c n (©). Mixing natural hydrocarbons ofhigh molecular weight © dun Sn (©) Electrolysis of water “ (© Reaction of salts like hydrides with water Which of the following statements in relation to the trogen atom is conees? 24, An inorganic compound gives off O, when heated, turns an acidic solution of KI violet and reduces acidified (@) 35, 3pand 3d orbitals all have the same energy nico Tica (©). 3sand3p orbitals are of lower energy than 3d orbital a x (© 3portital islowerin energy than 3d orbital (@ 80, ) KNO, (@)_ 3s orbital is lower in energy than 3p orbital © 10, (@) All ofthese 5.@OQO@ 6.@OOO 17.@O0OO 18.@OQO@ VY. @O0OO@ 20.@@O@_21.©@OO@ 2.@©OO_23.@OOO@_¥%4. @OOO ‘Space for Rough Work GP_3371 fe36_-_————__—_————————____________ DpP/ CC09 25, Hydrogen peronie acts both as an oxidising and as a 28, From the following statements regarding H,O>, choose the reducing agent depending upon the nature of the reacting incorrect statement species. In which of the following cases HO, acts aS @ (a) thas tobe stored in plastic or wax lined glass botles in reducing agent in acid medium? dark @ M0; ©) cao (©) Ithas tobe kept away fom dust (© ean act only asan oxidizing agent © soe © sof a (@) Tedecomposes on exposure to light 26. Choose the correct statement 29. When zeolite (hydrated sium aluminium silicate is teated ‘The reason for use of polyphosphates as water softening withhhard water the sodium ionsare exchanged with agents i, that . " coe (@) Htions () Cations (@)_ they form soluble complexes with anionic species (©) they precipitate out cationic species © 8042 ions (@ OFF ions (©) they precipitate out anionic species 30, Identity and yin following reaction, What isthe mixture (@)_ they form soluble complexes with cationic species of x and y called? 27, Which statement is wrong? CH) + HOG) Myx ry (@) Ordinary hydrogen isan equilibrium mixture of ortho and para hydrogen (@ x= CO,,y=HL0, water gas (©) Inorthohydrogen spin of wonucteisin samedirecion ©) * 0, sym gus (© Ortho and para forms donotresemblein theirchemical ©) water gas properties (@ x= Op y= Hy 9m gas (@ In para hydrogen spin of two nuclet is in opposite direzsion LEE 2 ©20OO B6O@OOO 27.@O0OOO BOOOO %. OOOO #.@O@O@ Gr DAILY PRACTICE PROBLEM DPP CHAPTERWISE 9 - CHEMISTRY Total Questions 30 Total Marks 120 Attempted [Correct Incorrect [Net Score Cut-off Score 40 [Qualifying Score 60 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End Time : CHEMISTRY (cc10 ‘SYLLABUS : The s-Block Elements Max, Marks : 120 Marking Scheme : (+ 4) for correct & (~1) for incorrect, Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. Alkali metals are generally extracted by 3. Strongest bond isin between (@) reduetion methods (@) CF () double decomposition methods ®) Na (©) displacement methods (©) Both (a) and (b) (@ electrolytic method's (@ None of above 2. Which ofthe following represents a correct sequence of 4 A metal salt solution forms a yellow precipitate with reducing power of the following elements? potassium chromate in acetic acid, a white precipitate with (@) Li>Cs>Rb il H,SO,, but gives no precipitate with NaCI. The metal 4b) Rb>Cs>Li salt solution will consist of (©) Cs>Li>Rb (@) PCO, ©) BCO, (@) Li>Rb>Cs (©) MgCO, (@) CaCO, 1. @0OO_2 ©OOO_3. OOOO _4 OOOO ‘Space for Rough Work 138. -_——<$NA DP PI CC10 5 10. Which ofthe following has lowest thermal stability ? @ LiCo; (©) NaxCOs (©) K,CO; (@_Rb:CO; ‘The first (IE, and second (IE) ionisation energies (kJ/mol) ‘of afew elements designated by Roman numerals are given. below. Which ofthese would be an alkali metal? E, E, @i BR oI © 1 7300 om % na, @ NV i633 ‘The solubilities of carbonates deerease down the magnesium ‘group due to a deerease in {)_hyeiration energies of cations (6) inter-ioni attraction {©)_ entropy of solution formation (@)._latice energies of solids KO, (potassium super oxide) isusedin oxygen cylinders in space and submarines because it {@)_ absorbs CO, and increases O, content (©) ciminates moisture (©) absorbs CO, (@)_ produces ozone. ‘Which one ofthe following slts doesnot impart colour to theflame ? @ KI ®) ia © Gc, @ Mec, ‘Amongst LiCl, RBCI, BeCl, and MgCl, the compounds, with the greatest and least ionic character respectively are: (@) LiCland REC (© RbCland BeCl; LL. Which of the following statements about Na;O, is not correct? (@)_Itis diamagnetic in nature (@) Itisderivative of HO, (©) Na,0 oxidise Cr to C103" in acid medi. (@) Its the superoxide of sodium 12. All ofthe following substances react with water. The pair that gives the same gaseous product is (@) KandKo, (@) NaandNa,0, (©) Caand Catt, @ Baand Bao, 13, Which is not correetly matched? (Basic strength Cs,0< Rb,0AlAl>Ga>Tl (©) B>Ga>Al>T1 (@ B>Gacal—F (6) —NR,>—OR>—F (©) 2 methyl-5-hydroxy-3- pentanone (© —NR,OR—ORGin>O>G, © G>Giy>@>6y ©) @>Gid>G>O) © G>@>iin> Gi 11, Thereason forthe loss of optical activity of lactic acid when (OH group is changed by His that (@) Chiral centre of the molecule is destroyed (©) Molecule acquires asymmetry (©) Dueto change in configuration (@ Structural change occurs 12, In Duma’s method for estimation of nitrogen, 0.25 g of an ‘organic compound gave 40 mL of nitrogen collected at 300 K temperature and 725 mm pressure. Ifthe aqueous tension at 300 K is 25 mm, the percentage of nitrogen in the ‘compound is @ 180 () 1676 © 1576 @ 1736 13. Sodium nitroprusside, when added to an alkaline solution of sulphide ions, produces purple colour ion due to the formation of (@)_NafFe(H,0), NOS} (©) Nag{Fe(EN),NOS] (©) Na,{Fe(H,0), NOS} (@)NaFe(CN),NOS] 14, The most satisfactory method to separate mixture of sugars, (2) fractional crystallisation (©) sublimation (©) chromatography (@ benedict reagent DPP/CC12 an 5. @0O@ 6 @OO@ 1.@@O@_U.@OO@ 7. @0O@ §& @O0OOO % Q0O@ 12.@@O@_13.©@OOO_14. @OOO ‘Space for Rough Work GP_3371 DPP/ CC12 18. 16. a. 18. 1». iH Tee ote eee eee med paadam ct ge (ely active compound Oy sega isi gem (© sracnic ine (0 adiceromete mite Base senso Hand (©) H-C W HCH, B) Hy cary “The staggered conformation of ethane is less stable than eclipsed conformation, because staggered conformation has torsional strain “The eclipsed conformation of ethane is more stable than staggered conformation, because eclipsed conformation has no torsional tain ‘The eclipsed conformation of ethane is more stable than staggered conformation eventhough the eclipsed conformation has torsional strain ‘The staggered conformation of ethane is mor stable than eclipsed conformation, because staggered conformation has no torsional stan, ‘The numberof asymmetric C-atom crated and number of posible stereoisomers when benl (PRCOCOPR) seduced with LAI, (a) 23 © © @ ) 2.2 24 32 isinthe order of 21, "The most suitable method of separation of 1: | mixture of @ B>A>O — %) ©>B>-~ axthoand ere ntoptencs i (©) (A)>(©>B) @) (A)>B)>© fa) romatography Which ofthe following biphenyls is optically active ? oa "OOD i: (@)_ Sublimation 22, InKjeldahl's method nitrogen present is estimated as @ @ Ny ©) NA, © No, (None of these 23, Which ofthe following sequence of T and F is correct for given statements. Here T stands for correct and F stands for false statement {© The more the number of contributing structures, the CO more is the resonance energy. Which ofthe fttowing compounds does not show ie eee Lasaime'stetornivogen) Gio The energy of aca arcte of te oul (he {© Phenyiydacine —(@)_Azohenzene ee et ‘The correct statement regarding the comparison of staggered and eclipsed conformation of ethane, is tre oars 15.@OQO@ 6.@OOO 17.@O0OO 18.@OQO@ 1. ©OOO 20.@@O@_21.©@OO@ 2.@©O@O_23.@OO@ ‘Space for Rough Work GP_3371 Ic DPP/CC12 24, Which ofthe following compounds undergoes nucleophilic 27, A similarity between optical and geometrical isomerism is substitution reaction most easily ? that (@) each forms equal number of isomers for a given : 0, (@_theyhave no similarity. 28, Arrange the carbanions, 1 (CHy)5C, Ec, (CH,),CH CHEM, (@) (CHy:CH > CCI, > CCH > (CH),C OcH, (b) CCI > CgHsCH, > (CH3)CH > (CH3)C 25, The stably of carbanions in the following (© (CHy,T> CHHy,CH> CGH, >Tc, @ ROC @ (@ CgHgCH, > Cer, > (CHy)sC> CH) 5H - 29, Chlorine in vinyl chloride is ess reactive because ) R,C= CH ™) Ric: (a) sp? - hybridised carbon has more acidic character than isin the order of: ‘sp? - hybridised carbon @ @>d>a>av) —&) ah>a>avy>) (©) C-C1bond develops partial double bond character © AVy>a>a>m —_ @) @>a)>ay>0V) (©) of resonance 26, The percentage ofsulphurin an organic compound whose (@) Allarecarrect O30 products 0233 of BaSO,{AL wt. Bae 137,S 32} 30 A.compound contains 38.8% C, 16% Hand 45.2% N. The is formula of compound would be @ 10 ©) 100 (@) CHNH () CHEN © 2s @ 21 (©) CyHgcN (@ CHYNH), 4@OQO@ 4@OQO@ %@O@OOO 27.©OOO 2%. @OO@ 26.@OO@_ W.©@OO@ Total Questions Attempted Incorrect [Net Score Cut-off Score Qualifying Score Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) [Correct ‘Space for Rough Work DPP - Daily Practice Problems Chapter-wise Sheets Start Time : End Time : CHEMISTRY (cc13 ‘SYLLABUS : Hydrocarbons Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. Inthe given reaction cH,CH,CH=cHcH; > CH CH,COOH +CH,COOH TheX is (@)CaHsONa (©) Cone. HCI +Anhy ZnCl, (©) Anh.AICl, (@) Kano OH" 2. Ethyl hydrogen sulphate is obtained by reaction of H,SO, (@)_Bihylene (©). Ethylchloride (®) Ethane (@) Ethanol 3 ‘One mole of a symmetrical alkene on ozonolysis gives two ‘moles of an aldehyde having a molecular mass of 44 u, The alkenes (@)_propene ©) Lbutene (©) 2batene (@) ethene Benzene on reaction with ozone forms (@) 2molecules of aldehyde and I molecule of ketone (@) 2 molecules of ketone and 1 molecule of aldehyde (©) wiozonide (@) hexaozonide 1 QDOO _2 ©OOO_3. OOOO _4 OOO ‘Space for Rough Work [oso 2 9% When neo-pentyi bromide is subjected to Wurtz reaction, the product formed is G@) 2.24-teramethyihexane (©) 2,244-tetramethylpentane (© 2255-teramethylhexane @ 2233-eramethyhexane ‘Which one ofthe following reactions is expected toreadily givea hydrocarbon product in good yields ? lecrolytie ©) RCO" Ag*—B2> @ RCOoK (@ CHsCHy;—S @ (CH3),¢c. ‘What wil be the product inthe following reaction? co sas Br cut, “de + Br on, © cr © Oo Be ‘A hydrocarbon contains 10.5 gcarbon and I ghydrogen. Is (0.36 has UL volume at 1 atm and 127°C, hydrocarbon is: @ CH, ©) CH, © CH (@ None of these ‘The conversion of 2, 3-dibromobutane to 2-butene with Zn and alcohol is (@) redox reaction (© Beelimination (©) ceelimination (@) Both (@) and (b) DPP/ CC13 10. 1,2-Dibromocyclohexane on dehydrobromination gives “oO oO “O (@ None of these AL C(H,CH, S22 7, In the given sequence Zs: (@)_ benzaldehyde (©) toluie acid (©) phenyl acetic acid (@) benzoic acid 12. Acid catalyzed hydration of alkenes except ethene leads to the formation of| (2) mixture of secondary and tertiary alcohols (©) mixture of primary and secondary aleahols (©) secondary or tertiary alcohol (© primary aleohol 13. Which of the following organic compounds has same hybridization as its combustion product (CO,)? (@) Ethane (&) Ethyne (© Bshene (@) Ethanol 14, In reaction sequence pecs CH;0H cH, prot 80, o 20, @ ALHC-C=CHB on 80, () ALHLC-E=CHyB:YC-C= CH Ea © © A:HyC-C=CHB: HC-C= cH, on ° (-ALH.C-C= CHB: HyC-C-CHy i 80 ————— oa | A group wi coil fu deactivates the benzene ring towards electrophilic substitution but which directs the {incoming group principally othe o- and p-pesitions is @ -NH, co © -No, @ CH, Inthe reaction jy QNANH. /ligNHs _ ()NaNHy /tig NH (QCH:CH Br Q)CH;CH3Br XandY are @ (b) X=2-Butyne; ¥ =3-Hexyne X= I-Buyne; ¥ =3-Hegne L-Butyne: ¥ =2-Hexyne "The main product of the reaction is Na.NHsCO R MMO Product cucu ocr wa OWED AN ES, ce f GP © Ss is obtainalefrom azanlisof which ofthe following ete ‘compounds ? 23. Inthe following reaction, the major product is "Sy Hye lh cH, ® ® cH, ne wa sive ey cu, a 6 OCD des af cit @ He » & p-PF ‘Which of the fottowing reagents convert propene to a net anuoTnso! (©) Aqueous KOH cH, B (©) MgSO, NaBH/H,0 (@) ByHy.H,0,,OH- © © : raat one ee ero acAAw © ye-Ns 24, Which ofthese wil nt react wth acetylene? ® © oS (@ NaOH (@) ammonical AgNO, © MN @ ma PR 15.000 6OOOO 17.0000 B.OOOO Y. OOOO fern 20.@OOO_11.©@0OO_2O©0OO_23@0@O@_ 4 OOOO ‘Space for Rough Work Jos DPP/ CC13 CH, -CH=CH, cit, CH =, 2. * on mercuration-demercuration 28. +HCL—> x, Xis produces the major product: ca, eC CH, -CH-CH, CH) ~CH,~CH,CL ® on a @ © © uci, chy cit, -CH=CH, © bn On J “Oo EN oh EOL TTL ee) 30, For the Sess ofthe following compound _ won, san oe HjC-C=CH cH,08 CHCA, HOW CaCl ons ‘Which method is best? ® ® cuts cacH cH, NBS. Cte), _NwOHE oy cA sta TL, ea an oO a'eS 7 27. The gas liberated by the electrolysis of Dipotassium Tat nd he ei Dio ene nara (@) Ethane ©) Eihyne Ho" © Ethene (@, Propene r 28, 1, 3-Butadiene when treated with Br, gives 5 iibromo-2-butene 3 dibromo-2-butene (a) Method 1 (b) Method It PO eee meen oto anteeae aes {© Bosh) and {@) Neither) nor (©) 3,4-dibeomo-L-butene (@) 2,3-dibromo-2-butene ey 3@QO@ WOOOO 27.©OOO BOOQOO %. OOOO 30.©@OO@ DAILY PRACTICE PROBLEM DPP CHAPTERWISE 13 - CHEMISTRY Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 35 Qualifying Score 50 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Max, Marks : 120 L Start Time : End CHEMISTRY [cc14 ‘SYLLABUS : Environmental Chemistry Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, High concentration of which ofthe following in atmosphere leads to stiffness of flower buds which eventually fall off from plants? (@) NO, ©) $0, © oe (@ Smeg Green house gases (@) allow shorter wavelength to enter earth's atmosphere while doesn't allow longer wavelength to leave the carth’s atmosphere, (b) allow longer wavelength to enter earth atmosphere ‘while doesn't allow shorter wavelength to leave the surface (©) don't have wavelength specific character. (@)_ show wavelength specific behaviour near the earth 3 4 while far from earth these have wavelength independent behaviour. ‘What is the concentration of dissolved oxygen in cold (@ Sppm (©, 200,000 ppm Sci is polluted by 1 pesticides IL synthetic fertizers ML green manure ‘Choose the correct option. (@) Landi (© Mandal (©) 10ppm (@ 10pm @) Tana (@ 1.Mand Mt men 41. ©QOOO_ 2 @OOO_3 @©O0OO_4 OOOO ‘Space for Rough Work 1054 -—————————_—_______________——_ DPP/ CC 14 5 2 9% 10. Water soften treated with chlorine to (@) remove hardness (©) increase oxygen content (©. killgerms (@) remove suspended particles ‘The substance which isa primary pollutant? @) H,SO, &) © ( FAN (@. Aldehydes ‘Which of the following is/are the hazardous pollutants) present in automobile exhaust gases? © N, @ © Gi) CH, (iv). Oxides of nitrogen @) Gianaciiy (© Giana iv) “Reducing potentially hazardous waste through smarter production”. ‘This represents a great step forward for (@) green revolution (b)_ green chemistry (©) industrial revolution (@)_ green biotechnology ‘When rain is accompanied bya thunderstorm, the collected ‘ain water will havea pH value @) slightly lower than that of rain water without thunderstorm (©) slightly higher than that when the thunderstorm is not there (©) uninfluenced by occurrence of thunderstorm (@) which depends upon the amount of dust in air ‘The irritant red haze in the traffic and congested places is due to presence of which of the following ? Oxides of sulphur 4) Oxides of nitrogen (Gi) Carbon dioxide un. 2. 13. 4 (iv) Mists, smoke and dust (9) Smog. (@ G@.Gvyand(v) ——@)_iidonly (©) Gi)only @ Gand Formation of photochemical smog takes place in (@) winter during day time (©) summer during morning time (©) summer during day time (@) winter during morning time 'B.OD. test or biochemical oxygen demand testis made for ‘measuring (@)sirpolluion (©) water pollution (©) noise pollution (@)_ sil pollution ‘The smog is essentially caused by the presence of (@) Oxides of sulphur and nitrogen (b) O,and Ny (© O,ando, @ Osan, ‘Which of the following statements about the depletion of ‘ozone layer is correct? (@) The problem of ozone depletion is les serious at poles because NO, solidifies and is not available for ‘consuming CIO" radical. (©) The problem of ozone depletion is more serious at poles because ice erystals in the clouds over poles act as catalyst for photochemical reactions involving the ‘decomposition of ozone of CI* and CIO" radicals. (©) Freons,chlorofluorocarbons, are inert. Chemically, they ‘do not react with ozone in stratosphere. (@)_ Oxides of nitrogen also do not react with ozone in stratosphere. an 5. @0O@ 6 @OO@ 1.@@O@_U.@OO@ 7. @0O@ §& @O0OOO % Q0O@ 12.©@©©@ 13.@@O@_14. @OOO@ ‘Space for Rough Work GP_3371 DPP/ CC14 A Aa ot 15, Ozone layer of stratosphere requires protection from indiscriminate use of (@) balloons (b) pesticides (©) atomic explosions (@) aerosols and high flying jets 16, Identify the incorrect statement from the following (a) Ozone absorbs the intense ultraviolet radiation ofthe Depletion of ozone layer is because of its chemical reactions with chlorofluoro alkanes. (©) Ozone absorbs infrared radiation. (@ Oxides of nitrogen in the atmosphere can cause the depletion of ozone layer. ‘Which of the following statements about polar stratosphere clouds (PSCs) is not correct? (a) PSCs do not react with chlorine nitrate and HCL (b) Type I clouds are formed at about -77°C and contain, solid HNO, .3H,0 (© Type tl clouds are formed at about ~85°C and contain, Atight whiripool of wind called Polar Vortex is formed Which surrounds Antarctica 18, Which ofthe following practices will not come under green chemistry? () If possible, making use of soap made of vegetable oils, instead of using synthetic detergents Using H,0) for bleaching purpose instead of using chlorine based bleaching agents (©) Using bicycles for travelling small distances instead o 1”. @ © @ 19. Phosphate fertilizers when added to water lads to (a) increased growth of deomposers (b) reced algal growth (© increased algal growth (@) tient enrichment (eutrophication) “Thermal pllcon affects mainly ~ (vegetation (aquatic erature © rocks @ ae 21. Roasting of sulphides give the gs Xa aby product. Tisis colekss gas vith coking smell oft sulphur andcaused reat damage to respiratory organs as result of acid ain. Its aqueous sluion is acd, acts as a reducing agent and its cid bes never been solted. The gas Xia «@) 80, © C0, © 80; @ Hs Scvnge waters poritied by (@) aquatic plans (0) micro-oganems © taht @ fishes Carbon monoxide (CO) isharmful to msn becase (@)itforms carblicacia (bit generates excess CO, (© itiscateinogenie (@) competes with O, fr haemoglobin Which on ofthe following statements sno tue? 6) Dissolved oxygen (DO) in cold water can reach a concetration upto 10 pp. (&) Clean water would havea BOD vale ofS ppm (©) Fiveride deficiencyin drinking water shart Soluble fhoride soften vod to bring is concentration wp Pom. of using petroV diesel based vehicles (©) When the pH of rain water is higher than 65, itiscalled Using plastic cans for neatly storing substances acid rain, .@OO@ 16.@OQO@ 17.@02OO 18@©OQO@ 19. @OOO 20.@@O@_21.©@OO@ 2.@©OO_23.@OOO@_¥%4. @OOO ‘Space for Rough Work 1656 -—_—_———_—______———— DPP/ CC 14 25, Frequent occurrence of water blooms in alake indicates 28. Which one ofthe following statement isnot true? (@) nutrient deficiency (@) pHofdrinking water should be berween 55-95. (©) oxygen deficiency (©) Concentration of DO below 6 ppm is good forthe (©) excessive nutrient availabilty stowth of fish @ ahuence of herbivores in the lak (©) Clean water wouldhavea BOD value oflessthan 5 ppm. (@) Oxides of sulphur, nitrogen and carbon are the most 26, Which of following no common component of Seaeett ai Photochemical smog! 29, A dental disease characterised by mottling ofteeth is due to (@) Ozone presence of a certain chemical element in drinking water. () Acrolein ‘Which is that element? (©) Peroxyacetyl nitrate (@) Boron (©) Chlorine (@) Chloroftuorocarbons (©) Fluorine (@ Mercury 27. Which ofthe following isa sink for CO? 30, Minamata disease is due to pollution of (a), Microorganism present inthe soil (a) aresenic into the atmosphere (b) Oceans, (©) organic waste into drinking water (©) Plants (©) oilspill in water (@) Haemoglobin (@) industrial waste mercury into fishing water Pe 25.©O00O U@OOO 27.©OHOO B.@OOO Y%. O@OOO 30.@OOO a DAILY PRACTICE PROBLEM DPP CHAPTERWISE 14 - CHEMISTRY Total Questions Total Marks Attempted Correct Incorrect Net Score Cut-off Score 40 Qualifying Score 60 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Max, Marks : 120 Start Time = End CHEMISTRY (cc15 ‘SYLLABUS : The Solid State Marking Scheme : (+ 4) for correct & (~1) for incorrect answer Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. 1fGermanium crytallises in the same way as diamond, then “which ofthe following statement is not correct? @ o © @ Every atom in the structure i tetrahedrally bonded to atoms. Unit cell consists of Ge atoms and co-ordination number is 4 All the octahedral voids are occupied. All the octahedral voids and 50% tetrahedral voids ‘remain unoccupied. 2 Thecubic uni cell ofa metal (molar mass = 63.55z mot") has an edge length of 362 pm. Its density is 8.92g om ‘The typeof unit cell is (@) primitive (©) face centered (©) body centered (@) end centered Doping of AgCl erystals with CdCI, results in (a) Frenkel defect (b) Schottky defect (©) Substitutional cation vacancy (@) Formation of F-centres ‘A metal crystallizes in 2 cubic phases foc and boc whose unit cell lengths are 3.5 A and 3.0A respectively. The ratio (oftheir densities is @ 07 () 208 © 146 @ 32 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work 88 A Aa$a —_ DPR CIB 5. Coordination numbers of Zn®* and S* in the crystal structure of wurtzite are @ 44 © &4 6 The coordination number X (. hanged t0Y (BY. @ () X=8toY = 6applying high pressure (©) X=6toY =8 applying high pressure (@) None of these © 66 @ 38 ) of each ion in KBr is oY =8 applying higher temperature 7. ‘The radius of Li* ion is 60pm and that of F- is 136 pm. ‘Structure of LiF and coordination number is (a) LikeNaCl,CNo.=6 — (b) Like CsCl,C.No.=8 (©) Anti fluoride, CNo.=8_ (@) None of these ‘8 Thenumber of carbon atoms per unit cel of diamond unit cell @s ©) 6 o1 @4 9. The pyknometric density of sodium chloride crystal is 2.165x 10 kg nr whileitsX-raydensityis 2.178 10° kg ‘The fraction of unoccupied sites in sodium chloride crystal (@) 596% 10% ©) 596108 © 596% 107 @ 596x104 10, Which of the folliowing metal oxides is anti-erromagneticin, nature? (@) Mn0, ©) To, © VO, @ 0, AL, Which ofthe following soldsisnot an electrical conductor? @ Mee © TOS © 40 @ 406 12, Ther, /1_ratio of ZnS is 0402. Pick out the false statements ofthe following (@) Zn$is4:4 coordination compound, (b) ZnS does not crystallize in rock sal type lattioe because +. /1_istoo small to avoid overlapping of $2 ions, (© Zx?* ions too small to fit precisely to the octahedral voids of ions. (@)_ Zn? ion is too large to fit into the octahedral voids of ‘sions. 13, Theunit cell dimensions ofa cubic lattice (edges, b, cand, the angles between them, a, B and) are @ arbeca 14, The pure crystalline substance on being heated gradually first forms a turbid liquid at constant temperature and silat higher temperature turbidity completely disappears. The behaviour isa characteristic of substance forming. () Liquid erystals (@ Isomorphous crystals (@) Allocropic erystals (©) Isomeric crystals an 5. @0O@ 6 @OO@ 1.@@O@_U.@OO@ 7. @0O@ §& @O0OOO % Q0O@ 12.@@O@_13.©@OOO_14. @OOO ‘Space for Rough Work GP_3371 DPP/ C15 —— tcc 15. 16. aw. 18. 19. 20, ‘To get a n-type semiconductor from silicon, it should be doped with a substance with valency @ 2 1 © 3 @s ‘The second order Bragg diffraction of X-rays with = 1.04 from a set of parallel planes in a metal occurs at an angle of 660°. The distance between the scattering planes inthe crystal (@) 0575A (b) L004, (©) 2004 @ 11sA ‘Which of the following oxides shows electrical properties likemetals ? @ SiO, (>) MgO © 80,6) @ GO, Al (at. wt 27) crystallizes in the cubic system with a cell edge of 405 A. Is density is 2.7 g per em’, Determine the unit a. (@) 041s ©) oss © >0731 @ 0731 “The incorrect statement forthe sulphur stom of ZaS is ‘As S® is larger than Zn?* only 4 rather than 6 oF 8 'S?> can be packed around Zn?* Its structure is similar to diamond except that alternate atoms are Zn and S @ © (©) As Sis larger than Zn?* only 6 rather than 8 oF 4 sulphide ions can be placed around Za?* ions (@) ZaSisa covalent compound 22. AB; crystallizes in a body centred cubic lattice with edge length ‘a’ equal to 387 pm. The distance between two ‘oppositely charged ions in the lattice is (@) 35pm —(b) 25pm (©) 20pm (A) 00pm aac ne mies CSAS 23, How many unit cells are present in a cube-shaped ideal yen een expt of NaC of mass 1.00 7 (©) bee, 1.432A @ fee, 1432 A [Atomic masses : Ni 3, C1=35.5) ‘The ratio of inner planar distances of three types of planes. (@) 5.14 10" unitcells (b) 1.28 x 10 unitcells (j09-4y 10-411) for simple cubic lattice are (©) 1.7110" unitcells (@) 257 10" unitcells : 24, Theimterone distance forcesium chloride ery Wil be @) 1: = a OB BE" @s ¢ © Bea Bi Vie 2a © o % Fora cubic geometyheimitn B@OOO 6OODOO 17.9GHOO 4%OOOO 1. OOOO 20.@@QO@O_1.©@OOO_2OOOO_3.@OO@_¥4. @OOO ‘Space for Rough Work 60. A —_ DP PI CCB 25, Forfecif ABis jus like the rock slike structurethen, A° __(a)_Na* ions are packed in ocshedral holes between the ‘and Bare located at~ planes of close-packed Cl-ions. @)_A*-Tetrahedral voids ;B--Comer (©) Za? ions are packed in tetrahedral ho (&)-A*-Comer and faces ; B-- Octahedral voids (© Cs* ions are packed in a simple cubic array of (© A*-Octahedral vids ; B-- Corner and faces crt (@)_A*-Comer and faces :B~-Octahedral and tetrahedral (Allo these voids 29, What ype of crystal defect is indicated in the diagram below? 26. Which of the following exists as covalent crystals inthe solid Na*Cl-Na*cr-Na‘ Cr state ? crO crn Nr (@) Todine () Silicon Na’ DICH Na*ct (© Sulphur (@) Phosphorus CE-Nat CrNa* [] Nat 27. ‘The packing fraction fora body-centred cubic is (@) Interstitial defect (@) 092 ©) 083 (b) Schottky defect © 068 (@ 082 (©) Frenkel defect 28. Consider the radii 0.095 nm (Na*), 0.181 nm (CI) (@) Frenkel & Schottky defects 0.074 nm (Za*), 0.184 nm (S*), 0.068 nm (Ti), 39, Whatis the coordination number of sodium in Na,O? 0.140 nm (O*>), 0.169 nm (Cs*). Choose the correct option, @ 6 4 : from among the following. (Use radius atiorules) one ane roe 25.©QOO© %@OOO@ 27.©@OOO B%OOOOD %. @OOO ol 30.OO0OO DAILY PRACTICE PROBLEM DPP CHAPTERWISE 15 - CHEMISTRY Total Questions Attempted [Correct Incorrect [Net Score | Cut-off Score 35 [Qualifying Score Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time = End CHEMISTRY (cc16 ‘SYLLABUS : Solutions Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Daly Practice Problem Sheet contains 30 MCQ's, For each question only one option is correct Darken the correct cicle/ bubble in the Response Grid provided on each page, 1, Thesolubilty of solidin aliguidis significantly affected (4) atc sluilty 7 stemperature t by temperature changes 2. The vapour pressure of a solution of the liquids A Solute + Solvent = Solution (p°=80mm He and x, =0.4) and B(p°= 120 mm Hg and ‘The system being in a dynamic equilibrium mus follow xy ~ 06) is fund to’be 100 mm Hg. It shows that the Le-chatelier’s principle. Considering the Le-chaeler’s solution exhibits Principle which ofthe following iscoret? (@) positive deviation fom ideal behaviour G@) AH) >0: solubility 7; temperature | (b) negative deviation from ideal behaviour () AH,.,<0; solubility | ; temperature T (©) ideal behaviour (© Att,y>O;solbiiy | :temperaturet (@ positive deviation for lower cone. and negative for higher 1. @0OO_2 @O@OO@ ‘Space for Rough Work be. -_—<$A A —— DPR CCB 2 1 Vs 5 (Xa mole ration ofA in Higud state and yg in vapour stat) is linear whose slope and intercept respectively are given Plot of = ope , PB @ ph sp, PRoPA * P Coolent used in car radiator is aqueous solution of ethylene slycol. In order to prevent the solution from freezing at =0.3°C. How much ethylene glycol must be added toS kg of | wwater?(K,= 1.86 K kg mot!) (@) 50 kg ©) 50g © 42 © 48 ‘A solution contains non-volatile solute of molecular mass. My. Which of the following can be used to calculate the ‘molecular mass of solute in terms of osmotic pressure ? @ M (22 )ver (My =(%2) 8 mm) (Win Henry's law constant of oxygens 14% 10-? mo. ic! atm! 1298 K. How much of oxygen is issolvedin 100ml at 298 when the partial pressure of oxygen is 0.5 atm? @ 14g ®) 328 © 24mg (@ 224mg ‘Whatisthe degre of disociation of sodium chloride, ifthe ‘molar mass determined bya eryosopie method was found to be 31.80 g mol [Atomic mass Na= 23 g mol! C1=35.5 g smot!}? (© M,=(™2 © m-[% er wm (@ 088 () 073 © a8 (@os2 8 Asolution containing components A and B follows Raoul’s awwhen (@) A—Battraction force is greater than A~Aand B-B (6) A~Battraction force is less than A—Aand B-B (©) A~Battraction force remains same as A~A and B-B (@) Volume of solution is different from sum of volume of. solute and solvent 9. ‘Two Itt flask Aand B are connected to each other by a valve which is closed. Flask A has benzene in equilibrium with ts vapours at 30°C. The flask B, is evacuated, and the valveis opened. Which ofthe following istrue temperature is kept constant.” @) Some of the benzene molecules would move to flask B from flask A. (©) Vapour pressure will be half the initial value (©) The vapour pressure remains unchanged (@ Some more of the liquid benzene in flask A would evaporate. 10, For a solution of two liquids A and B it was proved that .A(°4 ~P'p)+ P’p. The resulting solution will be (@) Non-ideal ©) ideal (©) semiideal (@) None of these 11, A 0.0020 m aqueous solution of an ionic compound ‘Co(NH),(NO,IC freezes at ~0,00732 °C. Number of moles ‘of ons which T mol of ionic compound produces on being issolved in water will be (Ky/=~1.86°C/m) @ 3 4 o1 @ 2 12, A solution of urea (mol. mass 56g mol“! boils at 100.18°C at the atmospheric pressure. If Ky and Ky, for water are 1,86 and 0.512 K kg mol respectively the above soltion will freeze at (@) 0658C &) -0654C (©) 658C @ ~654C an 3. @0O@ 4 OOOO 8 @OQO@_9 ©OO@ 5. @0O@ 6 @OOO 7. OO0O@ 1.©©O@_U.@OOO_V2. @OOO ‘Space for Rough Work GP_3371 DPP/ CC16 ——— ices 13, In mixture A and B components show-ve deviation as @ AV pin 0 ©) Api <0 (©) A~'B interaction is weaker than A - A and B~ B (@ A~B interaction is stronger than A ~ A and B~B interaction. All form ideal solution except (@) GHeand CH, CH, (©) GH, and 3H (©) GUsCland CgHBe (a) CoH, Land C,H, OH, ‘binary liquid solution is prepared by mixing n-heptane and ethanol. Which one of the following statements is correct regarding the behaviour of the solution’? (@) The solution is non-ideal, showing ~ ve deviation from Raoult’s Law, (©) The solution is non-ideal, showing + ve deviation from Raoult’s Law, (© mheptane shows + ve deviation while ethanol shows ve deviation from Raoult’s Law. (@) The solution formed isan ideal solution Ty 18. wv. a= Mole action 3-0 m=O ened Inthis figure, lines Iand II pass through the point for which. @* ‘Which ofthe folowing modes ofexpressing concentration is independent oftemperatre? @ Molarty () Molaliy (© Formality (@ Normality ow many grams of oncentated nic acid sltion should te tse toprepare 250 mL of 20M HNO, "The concentrated midis 708 HNO, {@) 900gco. HNO, ©. 340 geome HNO, (@) 70.0gcone. HNO; (@)_ 45.0gcone. HNO, 16, Wehave three aqueous solutions of NaC labelled as ‘A,B’ 21. Which among the following will show maximum axmotic and ‘C’ with concentrations 0.1M, 0.01M and 0.00iM, pressure? respectively. The value of van't Hoff factor for these (@) I MNACl & IMMgcI, solutions willbe in the order © LM(NH) PO, @) IMNayS0, @ igsipcic © igripric 22, The boiling point Of 0.2 mo kg solution of Xin water is (© inig=ic @) igsip>ic seater than equimoal solution of in water, Wich one of 17, During depression of freezing point in‘a solution the the following statements struc in this case? following ae in equilibrium (@) Molecular mass of Xs greater than te molecular mass (@) liquid soivent, oid solvent oY, (6) liquid sovent, soi solute (©) Molecular mas of Xis ess than the molecular mas of (©) liquid solute, slid solute ¥ (6) liquid sot, slid solvent (©) ¥ is undergoing dissociation in water while X 18. A plotof py orp, vs the mole rations x, and xis given undergoes no change se 5 (© Xisundergoing dissociation in wate. B@QQO@ M4.@OO@ 145.@OOO© 6 @OQO®@ 17.@O0OO 8.@OOO_19.©OOO _20.©OOO _21-©OOO_ 22. @O©OOO ‘Space for Rough Work be —<$N —_ DP PI CCB 23. Which ofthe following 0.10m aqueous solutions will have the lowest feezing point? @ ALSO) ©) Cyl. 0, © Ka © CH), 24. If sodium sulphate is considered to be completely lissociated into cations and anions in aqueous solution, the change in freezing point of water (A7), when 0.01 mol ‘of sodium sulphate is dissolved in 1 kg of Water, is (K,= 1.86 Kkgmd-!) @) 037K (@) 00558K (© 0omaK (@ 00186K 25, Which one ofthe following sls will have the same value of van't Hoff factor (as that of Kal Fe(CN). @ AlsSO., ® Na © ANO,); (@ NaSO, 26. Mole fraction ofthe solute in a 1.00 molal aqueous solution, (@) 0170 (6) 0017 © oon @ 1.7100 27. 253g of sodium carbonate, NayCO; isdissolved in enough water to make 250 mL of solution, If sodium carbonate lissociates completely, molar concentration of sodium ions, Nat and carbonate ions, CO} are respectively (Molar mass of Na,CO, = 106 g mol) (@) 0955Mand 910M (©) 1.910Mand0.955M (© 190Mand 1910M (@ 0877 Mand0477M 28, Azeotropic mixture of HCl and H,Ohas @ 48%6HO ) 22%HO (© 36%H8C1 (@ 22%HCL 29, Freezing point of an aqueous solution is ~ 0.186°C. If the values of K, and Ky of water are respectively 0.52 Kk mol"! and 1.86 K kg mot! then the elevation of boiling point ofthe solution in Kis @ 052 ©) 104 © 1s (@ 0052 30. Which of the following statements, regarding the mole fraction (x) of acomponentin solution, i incorrect? @ O05Ky>1 © AG*<0:Ky<1 (@ AG?>0:Ka<1 10. Standard "elgctrode potentials are “| Fe'/Fe [E*= 0.44]; Fe°¥VRe®? E° = + 0.77 : If Fe, Fe and Fe blocks are kept together, then (@)_ Fe’? increases () Fe? decreases Fe? © 7 remains unchanged (@ Fe? decreases electrolytic cell contains a solution of Ag,S0, and has platinum electrodes. A current is passed until 1.6 gm of O, hasbeen liberated at anode. The amount of silver deposited at cathode would be (@) 10788m ©) Légm (©) 08gm (© 21.60gm 12, IF @ denotes reduction potential, then which is true? ) Era = Voge Fen O) Ean = ren + Pipe ©) Frey Pin~ Vign — @ Eean =~ ent ¥ 13, Ina fuel cell methanol is used as fuel and oxygen gas i Used san oxidizer. The reaction is CH,OH() +320,(@)—> CO2(g) + 2H,000 ‘At 298 K standard Gibb's energies of formation for CH,OH(), H,0() and and CO, (g)are~1662-237.2 and-394.453 mot! respectively. Ifstandard enthalpy of combustion of methonal is~ 726K) mol, efficiency of the fuel cell willbe: @) 8% ) 90% © 9% © 9% 14, Forthe cell reaction, Cu Cy, aq) + Zs) = Zn** (Cy, ag) + Cu(s) of an electrochemical cell, the change in free energy, AG. ata given temperature isa function of @ Inc) ) n(Cyey © Inc) @ Inc +e) (©) AG*<0:Ky>1 a. 5. @QO@ 6 @OQO@ 0.@0@O0@ _1.@OO@ 7. @QO@ 8 @O0O@ 9% OOOO 2.©@@OO _B.@OO@_4. @©O@ ‘Space for Rough Work GP_3371 DPP/ C¢42] —— iii ter 15. 16. 1”. 18. 1. When electric current is passed through acidified water, 112 ml of hydrogen gas at STP collected atthe cathode in 1965 seconds. The current passed in amperes is @ 10 @0s @Ol @20 ‘The electrode potential , of a zinc electrode at (ca? fam) 25°C with an aqueous solution of 0.1 M ZnSO, is 2303RT (Eg pa) =~ O76. Assume =0.061298K} @ +073 ©) -079 © ~082 (@) -070 A gas Xat | atm is bubbled through a solution containing a mixture of 1M Y-and MZ>at25°C. Ifthe reduction potential ofZ>Y>X, then, (a) ¥ will oxidize X and notZ, (6) ¥ will oxidize Zand notX (©) ¥ will oxidize both X and Z. (a) will reduce both X and Z Fortheclactochemical ell, MM" |X" |X, E°M* /M=004Vand E° (XX)=033V. From this data one can deduce that (a) M+X-9M"+X- is the spontaneous reaction 21, Conductance of 0.1 M KCI (conductivity (©) MaQ; can be used in aqueous H,SO, (@) Cx0F can be used in aqueous H,S0, ‘Ahypatetical elecrcchemical cells shown below AJAT (xM)|IBY (yM)IB ‘Theemfmeasured is +0.20. The cell reactions @) Ate OAc oB (b) The cell reaction cannot be predicted (©) A+BYoA'sB @ A+BOASBY ‘Ohm fem filled in a conductivity cell is ¥ Ohm". Ifthe conductance of0.1 MNaOH filled in the same cells Z Ohm’ the molar conductance of NaOH will be XZ @ 2 © Zo 0% @ oF Y Y (On the tusis ofthe following E™ values, the strongest oxidizing agentis Feige IFN) +6035 Fore be: (©) M's 9M+X isthe spontaneous reaction © TCM OL (©) Eg=071V @ Fe (@ [FeCN @ Exy=-077V 23, The mathematical expression for law Of independent ‘Standifd cleewoae potential data are useful forunderstanding“~" gaigration of ions and Ostwald’ dilution law are given by {he suitability ofan oxidantin aedox tration. Some half cell ° reactions and their standard potentials are given below: @ A=A%,-BC* ©) Av =F, + UL) ‘M0 j(aq) +8H" (ag)}+5e” -> Mn?*(aq)) +4400) . Ao Age Beisiv © Ab=watv © AOAC ASe 2 . > 208" 24, The variation of equivalent conductance of strong (Cr0F (aq,)+ 14H" (aq.) + 627 > 2Cr** (ag) + 7H, 200) electrolyte with (concentration)" is represented by Fe (ag) +e" > Fe (ag) E°=07V vw, WZ Chi(g)+2e $2C1(aq)E*= 140 @* 4 Identify the only incorrect statement regarding the quantitative estimation of agueous Fa(N (2) MnO can be used in aqueous HCL 1 1 LL (b) Cr0}" can be used in aqueous HC] © all @ Ko Eo = PI OOOO KOOO@ 17.000@ B.OOOO 1. OOOO 20.@OQO@_21.©OOO 2.@OO@ B@©OOO@ 4. @OOO ‘Space for Rough Work hydrogen and methane, directly into electrical energy is known as: @) Electolyticcell (6) Dynamo (© NeCdcetl (@) FuelCell 5. Inacidie medium MnO, isan oxidant as MnO (3) +4H* +2e”——>Mn?* +20 If the pH of solution is decreased by one unit, the electrode potential of the half cell Pt: MnO, Mn?* will change by @ 0236V (b) -0236V © -0118v @ o118v Consider the following cell reaction: 2Fe(s)+Oy(g) + 4H (ag) > 2Fe™ (aq) +2H040:] At [Fe] = 103M, p(O,) = 0.1 atm and pl the cell potential at 25°Cis @ 1a1v © Lv © 187V @ 151V . In a hydrogen-oxygen fuel cell, combustion of hydrogen ‘occurs to (@) produce high purity water (b) create potential difference between two electrodes 1668. DPP/ CC 17 25. A device that converts energy of combustion of fuels like (©) generate heat (© remove adsorbed oxygen from electron surfaces ). Consider the following relations for emf of a electrochemical call: )emfofcell= (Oxidation potential of anode) — (Reduction Potential of cathode) (i) emforcell= (Oxidation potential of anode) + (Reduction potential of cathode) (Gi)_emfof cel = (Reduction potential of anode) + (Reduction potential of cathode) (Gv) emfofcell= (Oxidation potential of anode) — (Oxidation potential of cathode) Which of the above relations are correct? @ Gandy ©) Gidand © @ andi @ GivandGv) 1. Alydrogen gas electrode is made by dipping platinum wire {in a solution of HCI of pH = 10 and by passing hydrogen ‘208 around the platinum wire at one atm pressure. The ‘oxidation potential of electrode would be ? (@) 059V ©) ulsv. © Lsv @ 0059v B@OQOO %. OOOO 27.O@O0OO BO@O0OO %. @OOO Per 30.@OO@ GP_3371 PROBLEM DPI JAPTERWISE 17 Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 37 Qualifying Score 53 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work DPP - Daily Practice Problems Chapter-wise Sheets Start Time = End CHEMISTRY (cc's ‘SYLLABUS : Chemical Kinetics Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. The temperature dependence of rate constant (K) of @ chemical reactions written in ems Arthenius equation, k= Ae} Activation energy (E,) ofthe reaction canbe calculated by ploting 1 1 © WRF ) log k vs L © Wek Ge | @ kwT 2, Therateconstant ofthe reaction A> Bis046> 10-8 mol L~!S“ If the concentration of A is 5 M then concentration of B after 20 minutes is: @ 108M © 036M @) 360M @ 07M 3 ‘Thehal lif period for catalytic decomposition of AB at SO sm Hg is hrs and at 100 mm Hg tis 2 rs. The order of @1 @2 For the frst order reaction CyH,O(g)> CHa(g)+COG) the initial pressure of C,H,0() is 80 tore and total pressure atthe end of 20 ‘minutes is 120 tor. The time needed for 75% decomposition OR @o ‘of CHO would be : (@) 20minutes ©) 40minutes (©) 80minutes @ 120minutes 1. @0OO_2 @O@OO@ 3. @0OO@_4 ©©OO ‘Space for Rough Work 1¢-70-——_________________—— DPP/ CC18 5. ‘When a biochemical reaction is carried out in laboratory in the absence of enzyme then rate of reaction obtained is 10° times, then activation energy of reaction in the Presence ofenzymeis 6 om ()_ Different from E, obtained in laboratory (©) Pisrequired (@) Can't say anything In a reaction A —» Products, when start is made from 8.0% 10 MofA,halfifeis found tobe 120 minute. For the initial concentration 4.0 10-?M, the half-life ofthe reaction ‘becomes 240 minute. The oder ofthe reaction is @) 20 () one (©) two (a 05 Ina first-order reaction A — B, if kis rate constant and inital concentration ofthe reactant Ais 0.5 M., then the half- lites log 2 log? a eee eee ° k kos tno 0.693 Oe © OK ‘The rate expression forthe reaction A(G) + B(g)-2C1Q) is rate= KCl. What changes the nial concentrations ofA and B will cause the rate of reaction to increase by a factor of ight? a) C,x2;Cy2 (b) Cyx2; Cy (©) Cx: Cyd @) Cyx4sCyxd ‘The reaction A(g) + 2B(g) — C(g) + Dig) is an. clementary process nan experiment involving his eatcn, te Partial pressures of Aand Bare , ~ 0.60 atm and Eimrespectively When p= 0.20 am, teratof the reaction relative tothe inital ates 10, Select the rate law that corresponds to data shown for the following reaction A+B —> products. Ep (Al B)_ Initiatrate 1 012 oss = Od 2 0024 00m a8 3 oom 003 =O 4 0012 00m = a8 @ rate=KIBP o (©) tate=K{A][BP (@) rate=k[AP BE. 11, Arradicactive element gets spilled over the floor of room. Is, halflife periods 30 days. Ifthe initial velocity is ten times the permissible value, after how many days will it be safe toenter theroom? G@) 100days (©) 300 days () 1000 days (@) 10 days 12. "The energies of activation fr forward and reverse reactions for Ay + By = 2AB are 180 mot! and 200 k3 mol! respectively The presence ofa catalyst lowers the activation energy of harvard and ees) reactions by 10013 ‘The enthalpy change of the reaction (A, + By ® 2AB) in the presence of catalyst wll be (in KJ mol") @ » © © @ % 13, Consider the reaction Cls(aq) + H2S(ag) > $(s)-+211* (ag) +2CF (ag) ‘The rate equation for this reaction is HICH IHS} ‘Which ofthese mechanisms isare consistent with this rate equation? A. Cl +H > H* +CP +CI* + HS” (Glow) @ v6 @ v2 (©) 136 @ vig Ch AHS SHTSCr +S Gasty RESPONSE 5. @©O@ 6 @OO@ 7. ©OO@ 8 @OO@ % OOOO Gre 1.@0QO@O _1.©O@OO_2.OOOO_B.O0OO ‘Space for Rough Work GP_3371 DPP/ CC18 —— SA eri os 18. 16. 1. Bo HyS 2 Ht +HS"(astequilbsium) Cl +HS 42Cl +H" +S low) ©) Both AandB @ Acaly (@ Bonly (© Neither AnorB ‘The initial rates ofreaction 3A + 2B + C —> Products, at different initial concentrations are given below: Initialrate, —[AlyM_— [BlyM_— [ClyM Ms! 530x103 0010000510 50x10 010 ames 10x10? 00100010010. 125103 ons ons 010. ‘The order with respect to the reactants, A, B and C are respectively @ 32,0 @) 3,21 © 2,20 @ 21,0 In a reversible reaction the energy of activation of the forward reaction is 50 kcal. The energy of activation forthe reverse reaction will be (@) 50kcal Halflife period of fistorder reaction is 1386 seconds. The specific rate constant ofthe reaction i: (@) 05x10%s1 — () 05x 10354 © S0x10%s! — @ 50x10354 can be taken as the time taken for the concentration of a reactant to dop 0 3 ofitsinial value. the rate constant 18, Activation energy (E,) and rate constants (k, and ky) of a chemical reaction at two different temperatures (T, and T,) are related by fo k 119 @) in? =~ ) ink $ on Om iT 78 @ wha Foft 19 RE, hb 49. Consider a reaction aG + bH -> Products. When concentration of both the reactants G and His doubled, the rate increases by eight times. However, when concentration of G is doubled keeping the concentration of H fixed, the rate is doubled, The overall order ofthe reaction is @ 0 1 ©2 @ 3 20, ‘The rate law fora reaction between the substances A and B is given by Rate=k [AP [B]" On doubling the concentration of A and halving the concentration ofB, the ratio ofthe new rate tothe earlier rate (ofthe reaction will be as @ tn) © @-m 1 () 3 = @2 ©) avar 2, The rate constants k, and k; for two different reactions are 1089-2007 and 1085 e107, respectively. The temperature at which k, for a first order reaction is k, the ‘4 ‘can be written as 2000 1000, @ 079% ©) 069% © 100K ©) Z3q3% © AHOK Dy aq5K © 029k @ 010k H.@ODOOD B.OOOD 16.OOGOO 17.OOOO 18. OOOO V.@OOO _2.©OOO _21.©O0OO ‘Space for Rough Work 172 ——_______________——— DPP/ CC18 22, Match the columns @ k= 2M8jog!Rol Gq) Rate constant for 210 eR) order reaction (© Valueof kforfirst k= Ro 22 order reaction when ‘= a= lo ” mae (8). Rate constant for frst Wetrrtcdonien © Rasa te tygan = BD (a) A~(s),B-(q),C~(p),D-() 0) A-@.B-(),C-(p),D-@ (© A-@,.B-(),C-G),D-@ (@ A-@.B~(),C-(),D-@) 23, The slope in Arthenius plot, is equal t: z, E, @ - Ea y 2.303R oO R R © aes (@ None of these 24, Forthe reaction A+B —> products its observed that: (1) On doubling the initial concentration of A only, the rate of reaction is also doubled and. @)_Ondoubling the initial concentrations ofboth A and B, there isa change by a factor of8in the rate of the reaction. ‘The rate of this reaction is given by G@) rate=K{A}[BP(b) rate=K (A)? [BP (© rate=k(A}[B] @ rate=k(AP(B) rate and rate 2S. For the reaction 2Nz05 ->4NOz +03 , ‘constant are 1,02 x 10- mol lit" sec“! and 3.4%10° sec“! respectively then concentration of NO, at that ime will he (@) L732M (© 34x10 () 3M @ 102%104M 26. 30. “The given reaction 2FeCl; +SnCl; —9 FeCl +: isan example of (@) firstorder reaction (©) third order reaction SnCly () second order reaction (@ None of these Consider the reaction Ny(@) 13H, @) > 2NH,(@) espa atntipbawes AMES! yg Hal i k 4, SINH3]__ 20H} 4, dINHs) __ 3 ditty) o) dt dt dt go SMHal, Ha) ANH] a at as a Which ofthe following statements is incorrect? (@) Activation energy for the forward reaction equals to activation energy for the reverse reaction (b) For a reversible reaction, an increase in temperature increases the reaction rate for both the forward and the backward reaction (©) The larger the initial reactant concentration fora second ‘order reaction, the shorter sits half-life. (® When Atis infinitesimally small, the average rate equals the instantaneous rate 3A +B +C, it would be a zero order reaction when (@)_ the rate of reaction is proportional to square of ‘concentration of A (©) therate of reaction remains same at any concentration of (©) the rate remains unchanged at any concentration of B and C (@) the rate of reaction doubles if concentration of B is increased to double ‘The decomposition ofa substance follows first order kinetics. Its concentration is reduced to 1/8th ofits inital value in 24 ‘minutes, The rate constant ofthe decompexiton process is 0.692 int 2692 sin @ 12min w 230 6(2)in! gy 228 oO A @ Ss (§) aie Pere fer 2.@@O@ 23.@@O@ 27.©OO@ _2%.O@0@O@ DAILY PRACTICE PROBLEM DPP. ZOOOO 3@OO@ 2%. BOOS 29.@OOO _30.©@OOO CHAPTERWISE 18 - CHEMISTRY Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 38 Qualifying Score 56 Success Gap = Net Score — Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End CHEMISTRY (cc19 ‘SYLLABUS : Surface Chemistry Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, L_ Which of the following electrolytes is least effective in coagulating ferric hydroxide solution? (@) KBr () K,S0, © K,C10, (@ Kg(PACNg) 2 CodLivercilis (@) fat dispersed in water (b) water dispersed in fat. (©) water dispersed in oil (0) fat dispersed in fat 3. One desires to prepare a positively charged sol of silver iodide. This can be achieved by (@) adding small amount of AgNO, solution to KI solution (©) mixing equal volumes of equimolar solutions of AgNO, and KI (@_ None of these ‘Which ofthe following statements is no true about the oil: in-water type emulsion? (@) Onaddltion of small amount of water, no separate layer ‘of water appears (©) Onaddition of oi, separate layer of oli formed (©) Addition of an electrolyte causes the conductivity of inslight excess the emulsion to increase (@) adding small amount of KI solution AgNO, solution (@ Addition of small amount of oil soluble dye renders in light excess the entire emulsion coloured. Peau | ©OOO 2 @O0©OO 3 @0OO 4 OOOO ‘Space for Rough Work lor S. Freundlich equation fr adsorption of gases (in amount of) ‘on solid Gin amount of mg) at constant temperature canbe expressed as x 1 x 1 (@) Wop%=togp+Liogk (>) tog+=togk +t p © Sap" @ 6 Thesize of colloidal particles is ofthe order (@) >O1n (6) Impt00.2,. © <1mp (@ >10mp 7. Which of the following constitutes irreversible colloidal system in water as dispersion medium? (@) Chay () Platina (©) FeOH), (@ Allofthese 8 Which ofthe following forms cationic micelles above certain ‘concentration’? (@) Sodium dodecyl sulphate ©) Sodiumacetate © Urea (@_Cetyltrimethy| ammonium bromide 9. Position of non-polar and polar pat in micelle is (@)_ polar atouter surface and non-polar at inner surface (®) polar atinner surface and non-polar at outer surface (©) distributed all over the surface (@ present in the surface only 10. ‘The cause of Brownian movement is (a) Heat changes in liquid state (©) Convectional currents (©) The impact of molecules ofthe dispersion medium on the colloidal particle. (@) Attractive forces between the colloidal particles and molecules of dispersion medium. DPP/ CC19 AL, Which of the following curves is in accordance with Freundlich adsorption isotherm ? @ © @ Tee > Tap 12. A colloidal solution is subjected to an electrical field. The particles move towards anode. The coagulation of same sol is studied using NaCI, BaCl, and AICI, solutions. Their coagulating power should be (@) NaCI> BaC, > AIC, (6) BaCh,> AIC, > NaCl (©) AICI, >BaCl, >NaCl (@ BaCl, >NaCl>alC, 13, Which of the following is most effective in causing the coagulation of ferric hydroxide sol? @ ka ©) KNO, © KO, (@) K,IFACN)) 14, Alum helps in purifying water by (@) forming Si complex with clay particles (b) sulphate part which combines with the dirt and removes, (© aluminium which coagulates the mud particles (@) making mud water soluble 3 QOOO 6 OOOO 1.@@O@_U.@OO@ 7. @0O@ §& @O0OOO % Q0O@ 12.@@O@_13.©@OOO_14. @OOO ‘Space for Rough Work GP_3371 DPP/ CC19 ——— ers 18, 16. a. 18. 9. 20. ‘Which is not correct regarding the adsorption ofa gas on, surface of solid? (@) On increasing temperature, adsorption increases continuously (b)_Enthalpy and entropy changes are ~ve (©) Mixing the sols has no effect (©) Sodium sulphate solution causes coagulation in both sols (@) Magnesium chloride solution coagulates, the gold sol ‘more readily than the iron (I) hytroxide so. (©) Adsorption is more for some specific substances 21. Which ofthe following will show Tyndall eect? (@ This phenomenon isreverble (@) Aqueous solution of sap below critical micelle The hats of adsorption n physiorption ein the angen coacentation ial) (©) Aqueous solution of soap above critical micelle (a) 40-400 (b) 40-100, ‘concentration. © 10-0 @ 1-10 (©. Aqueous solution of sodinm ehlride, Example fintrnsc colloids (@) Aqueous solution of sugar. (a) glue (®) sulphur 22, If.x is amount of adsorbate and m is amount of adsorbent, © Fe @) As,S; which of the following relations is not related to adsorption Foradsrpion ofa gas on asolid theplotoflog/mvslog process? Pis linear with slopeequalto(abeing whole numb) ©. /m=f(p)atcostaneT @ er ©) ek ©) x/m=fCtyat constant. on a (© p=f(T)at constant (x/ m). Which of the following statements is incorrect? es (@) Colloidal gids used fr intamscularinjection, 23. Tn Langimis mode of adsorption oa gas on solid urace (©) Colloidal solution of latex is used in preparation of (the mass of ps srking a given area of snice is rubber proportional tothe presse ofthe zs (© Photographic films are prepared by coating an (b) the mass of gas striking a given area of surface is emulsion of AgBr in gelatin over glass plate. independent of the pressure of the gas (© Tannin used in leather industry contains positively _-©_the rate of dissociation of adsorbed molecules fom ae the surface doesnot depend onthe surface covered ‘The disperse phase in colloidal iron (III) hydroxide and (@) the adsorption at a’ cingle site’ on the susface ny colloidal gold i positively and negatively charged, 44, tvoWemuline moeclesathesanetine Ce ay erat . Which ofthe following gus molecules have maximum value tepals Wn he wing sateen s NOT 2% Whe wings (@) Coagulation in both sols can be brought about by ® Call ) Ne electrophoresis © Ho ow B.@ODOO 6.OOOD 17.OOGOD BOOOO 1. OOOO 20.@@O@_21.©@OO@ 2.@©OO_23.@OOO@_¥%4. @OOO ‘Space for Rough Work 16-76 -—________________——_ DPP/ CC 19 25. Which one of the following statements is not correct?” 28, At high pressure, the entire surface gets covered by a (@)_ The value of equilibrium constant is changed in the monomolecular layer ofthe gas follows presence of catalyst inthe reaction at equilibrium (@) three-halvedorder(B) second-order (b) Enzymes catalyse mainly bio-chemical reactions (©) firstordee (@) rero-ocder (© Coenzymes increase the catalytic activity of enzyme 29, Atthe Critical Micelle Concentration (CMC) the surfactant (@ Catalyst does no initiate any reat molecules 26, Among the electrolytes NaS0,, CaCl, Al(S0,), and _(@)- decompose NH,Cl, the most effective ing agent for SbyS3 sol (@)_ dissociate is (© associate (@) Na,S0, © GC, (@)_become completely soluble © AlxS0y), @ Nia 30. Peptization involves 27. Which ofthe following is not a favourable condition for (precipitation of colloidal particles physical adsorption ? (b) disintegration of ol (@) High pressure (©) evaporation of dispes (0) Negative AH (@) impact of molecules ofthe dispersion. medium on the (© Higher critical temperature of adsorbate colloidal particles (@)_ High temperature Resrows QQO@ % OOOO 7.O©OOO BOOOO %. OOOO 3#0.@OQOO DAILY PRACTICE PROBLEM DPP CHAPTERWISE 19 - CHEIMISTRY Total Questions 30 Total Marks Attempted [Correct | Incorrect [Net Score Cut-off Score 40 [Qualifying Score Success Gap = Net Score ~ Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End Time : CHEMISTRY (cc20 ‘SYLLABUS : General Principles and Processes of Isolation of Elements Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. Identity x,y 2 forthe following metallurgical process. ‘Metal sulphide _*, Metal oxide Impure metal 2 Pare metal x yand zare respectively (@) roasting, smelting, electrolysis () roasting, calcination, smelting (©) calcination, auto-eduction, bassemerisation (@)_ none of the above is correct 2, Bronzeisa mixture of (@) Po+Sn (©) Cu+Sn © Cu+Zn © Po+Zn ‘Which reagent is used in Bayer's process? (@) Na,CO, ©) Carbon (© NsOH @ Silica ‘Thomas slag is (@) CaPO), ©) CASIO, (©) Mixture ofa) and (6) @ Fs0, 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work 1678 - —. DP PRP CC20 5. 2 10. Which ofthe following condition favours the reduction of ‘ametal oxide tometal? G@)_AH= +ve, TAS = + veat low temperature () AH= +e, TAS =~ veat any temperature (©) AH=-ve, TAS =— veat high temperature (@)_ AH=-ve, TAS = + veat any temperature ‘Which of the following fluxes is used to remove acidic impurities in metallurgical process? (a) Silica (b) Lime stone for the reaction 1 @ Mgt 50, > Mg0 1 (©) 2Ag+ 502 > A830 1 @) C+5024CO © C+302 L @ 0+ 50) > 00, (© Sodium chloride 12, Which of the following elements is present asthe impurity (©) Sodium carbonate ‘othemaximum extentin the pig iron? ‘A basic lining is given toa furnace by using (@) Manganese (&) Carbon {@) Caleineddalomite (© Silicon (@) Phosphorus () Limestone 13. Among the following statements the incorret one is (©) haematite (@) Calamine and siderite are carbonates @ silica (©) Argentite and cuprite are oxides Electromagnetic separation is used in theconcentration of) Zinc blende and iron pyites are sulphides (@) copper pyrites (b) bauxite (@) Malachite and azurite are ores of copper (©) cassiterte (® cinnabar 414, Match list I with list I and select the correct answer using Extraction of gold and sive invalves leaching with CN the ees ven below theists: i ee 1 Cyanide process A Ultrapure Ge @ disitation IL Floatation process B. Pinecil (©) zonerefining Ml, Electrolyticreduction __C. Extraction of Al (©) displacement with Za 1. Zone refining D. Extraction of Au (@) liqution Codes: Which ofthe following eactionsisanexampleforcalcination —(@®) FG IFA,IIED,IV-B—(b) FDJLBIILCIV-A coca © ECIRILDIV-A —— (@) EDIFAIKCIVB Go) 2Ag+2HC1+(0)-> 2AgC1+450 3S: coupled antons tates place a flow (©) 2Zn+0, +2200 D+E—>F for the spontaneity of reaction A+ B-+E > C+, (©) 22n8+303 + 22n0+ 250, which of the following is correct? (@) MgCO; + Mz0+-C0: @ wey ) xy ° 2 @ xy (@ x=Q)«Tas A.G* vsTplotin the Ellinham’s diagram slopes downvard 16, _Aluminiumis extracted from alumina AI,O; )by electrolysis — 5. @©O@ 6 @OO@ 7. @O0OOO© 8% OOOO % OOOO W.@OOO U.OOOO 2.OOG0OO BOOGOO 4. OOOO 5.@OOO ‘Space for Rough Work GP_3371 DPP/ CC20 ————— oor ‘ofamolten mixture of ore, the oxidising and reducing agents used are ANO, NA, Gy” Oyand Coreen (b) AIO, +CaF, + NaAI, (@) 0, and Zn dust respectively (© AIO, +Na,AIF, + CaF, (©) HNO, and Zn dust respectively (@) MORE NS Ary (®) HNOSandCOrepetney 17. Wale oft faving rattnenis st he avenge of 21. Theme iienhich anotberedcedto meal byaatn ronnie oe tetas sn? i (@) FeO, ©) ALO; (The of oft supidesgreaerthan hoe fr CS, wo eee ants 22 Which flowing rein es plas in as uae Singer cer? 0) The AGP neve froasingotaipiteeewoxde. — AMMESKEaCtmotsme? (©) Roasting of the sulphide to the oxide is thermodynamically_ (bo) 2FeS +302 —> 2FeO + 280 tee (© 2ca0+Cu58—6C0+50, (@ Carbon and hydrogen are suitable reducing agents for (@)_ All ofthese reduction of metal sulphides. 23, Which process represents the change, 18 tatccurstonseper om spies heealis— T2 +, 92 fnlycined bythe ceases Gy Code (0 Copper saphie cn) ere () Sulphur dioxide ($0) (© Polling ©) ena) i ing oles aaecaey a meta ptt 19. The method of zone refining of metals is based on the Se Garni SEE Tat Te ol oe tt anette ee ean ee (a) Greater solubility of the impurity in the molten state ae Paar (1043048103 0 ey05.220 (Grater mosty afte pre meal than a ofthe Cad.K0 ince my (©, Higher weiog ponte impute hotihe 2S Wish ofthe lowing sof msi pried by ran nome (a) GaandIn (b) Zrand Ti (@) Greer characte tthe said ta han at of a © AgiAn—G@) NiandFe 20. tothe cj xan poses five om agente REI D059 1.ODOD BOOST V.DOOD % GOOD ferry 21.@@O@_2.©@@O@ 23.@©OO _4@OO@ _%. @OOO ‘Space for Rough Work 880.-_$@$Aj iia __€_———- PP? C020 26. Which of the following reaction(s) occur in temperature range 500 - 800 K in blast furnace @ Fe0;+CO—42Fe0 + CO, Gi) Fe0,+4CO—>3Fe + 460, Gi) Fe0+CO—+Fe+C0, iv) C+#CO,—+20 @ @amadi ©) @,Gianadiiy © Giiyanaivy @ Gvyonly 27. Which ofthe following pairis incorrectly matched ? (@) MagnetiteFej0, (b) Copper glance ~Cu,S (© Calamine-ZnCO; —(@).Zincite~ZnS 28, Before introducing FeO in blast furnace, itis converted to Fe,0, by roasting so that (@) itmay not be removed as slag with silica (b) it may not evaporate inthe furnace (©) presence oft may inerease the m.pt. of charge (@) None of these. 29. Which of the following statements is correct ? (@) Ganguesare crefilly chosen o combine withthe slag preset inthe oreo produce easily fusible ux tocarry away the impurities (©) Stags are carefully chosen to combine withthe fx present in the ore to produce easily fusible gangue to carry avay the impurities (©) Ganguesare carefully chosen to combine with the ux present in the ore to produce easily fusible slag to carry avay the impurities (©) Fluxes are carefully chosen tocombine wit the gangue present in the ore to produce easily fusible slag to carry away the impurities 30, The val of AG for formation of Cr, is S40 kImot and that of AI,0,is-827 kJ mol, What is the value of 4,6" for the reaction? £ ate) <2 c,0,09) + 2 ao309)+ Sex) FANG) + ZCh050) > [A030 +4 287K mol! 287k mol! (@) 574K mot" © (© +5744 mo! © 2%6.@QO@_27.©O0OO RID Total Questions 30 DAILY PRACTICE PROBLEM DPP Total Marks 28.@OO@ 2.@OO@ _3. ©OO@ OAL Oe Attempted [Correct Incorrect [Net Score Cut-off Score 38 Qualifying Score Success Gap = Net Score — Qualifying Score 56 Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End CHEMISTRY (cc21 ‘SYLLABUS : The p-Block Elements (Group 15, 16, 17 and 18) Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1L. The oxyacid of phosphorous in which phosphorous has 3. Thedeep blue colour produced on adding excess of ammonia thetowex oxidation stata to cope supe de to pesnce oF a) ypophosphoros aid " ©) ebephoporc sis @ a © cuovenys {© yrophoshore aid © cucntty3* © cant? (@)_metaphosphoricacid 2. The decreasing values of bond angles from NH, (106") to ‘SbH, (101°) down group-15 ofthe periodic table is due to (@) decreasing ip-bp repulsion ae (©) 6 double bonds; 6 single bonds a (©) 3 double bonds; 12 single bonds (@) increasing p-rbital character insp* ON a haa) 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work 4. Inacyclotrimetaphosphoricacid molecule, how many single ‘and double bonds are present? (@) 3 double bonds; 9 single bonds In nitroprusside ion, the iron and NO exist as Fe"? and NO" rather than Fe'** and NO. These forms can be differentiated by () estimating the concentration of ion (b) measuring the concentration of CN~ (©) measuring the solid state magnetic moment (@) thermally deccmpcsing the compound ‘The brown ring test for NO; and NO} is due t the formation of complexion with a formula (@) [FeO (b) [FaNO\CN),) (©) [Fe(H,0).NO}* (a) [Fe(H,OXNO),* Which compound is used in photography? (@) NaSO, () NayS,05 (© Na,S,0, (@ Na,S,0; Concentrated hydrochloric acid when kept in open air sometimes produces a cloud of white fumes, The explanation for tis that (@)_ oxygen in air reacts with the emitted HCI gas to forma cloud of chlorine gas (©) strong affinity of HCI gas for moisture i si results in forming of droplets of liquid solution which appears ike cloudy smoke, (© due to strong affinity for water, concentrated hydrochloric acid pulls moisture of air towards itself, ‘This moisture forms droplets of water and hence the cloud. (@ concentrated hydrochloric acid emits strongly smelling HCI gasall thetime. 1¢82-——$<<$< __—_—_————————____—_——— DPP/ €C21 9. Thehybridization in ICI, is @) spb &) dsp) © spd @ sp 10. The compound of sulphur that can be used as refrigerant is, (@ $0, () $0, © SA, @ 10, AL. Which ofthe following isa saline oxide ? (@) Na0, () Bao, © Nao @ FeO, 12. Which one of the following substances has the highest, proton affinity ? @ HS ()NH, © PH, @HO 13. Which one ofthe following statement regarding helium is, incorrect?” (@) It is used to produce and sustain powerful superconducting magnets (0) It is used as a cryogenic agent for carrying out ‘experimentsat low temperatures (©) Its used to fill gas balloons instead of hydrogen because itis lighter andnon-inflammable (@ tis used in gas-cooled nuclear reactors 14, Caro’saci (®) 1,80; (©) H;S,0, (© H,S0, © HS,05 an 5. @0O@ 6 @OO@ 1.@@O@_U.@OO@ 7. @0O@ §& @O0OOO % Q0O@ 12.@@O@_13.©@OOO_14. @OOO ‘Space for Rough Work GP_3371 DPP/ C¢214. ——RRA-p.T€_ A —_— Ht 18. The acid which forms two series of sats is (@) HPO, ©) HPO, © HBO, (@) HPO; 16, Which of the following species is nota pseudo halide @ NO () RCO © ON @ NNN 417. Gaseous HCL is a poor conductor of electricity while its aqueous solution is a good conductor this is because (@) HO is a good conductor of electricity (©) a gas cannot conduct electricity but aliquid can (©) HCI gas does not obey Ohm’s law, whereas the solution does (@ HCl ionises in aqueous solution 18. The number of hydrogen atom(s) attached to phosphorus atom in hypophosphorous acid is. @) three ©) one © two © 20 19. What products are expected from the disproportionation reaction of hypochlorous acid? (@ HClandc,0 (©) HClandHC1O, (©) HCIO,and,0 (@_ HCO, and HCIO, 21, Yellowammonium sulphideis @ (NHA)25, (©) (NH,)3S (© (NHy)25y (© (NH4)2Ss 22, Thecorrect order of increasing bond angles inthe following species are (@ C1,0< C10, < C103 (@) ClO, 2Xe+XeO3 +12HF +150, (©) 2Xek, +2H;0——+2Xe+4HF 40, (© XeFy+RBF—>RbIXeF)) (@) Xe03 +6HF—>XeF, +3430 24, Trigonal bipyramidal geometry is shown by: 20. Shape of XeOF, is (@) XeOsF, (@) octahedral () Xe0,F, (©) square pyramidal (© Fxe0S0,F (© pyramidal @ (XerP (@) Tshaped 5.@OQO@ 6.@OOO 17.@O0OO 18.@OQO@ VY. @O0OO@ 20.@O@O@ _21.@O0OO_2.@0OO_3.@O0@OO@_ 4. ©OOO ‘Space for Rough Work 1684. ___—_—————____—____——— DPP/ €C21 2S, Which of the following is used to produce and sustain (a) HOCIO.< HOC < HOCIO, < HOCIO, powerful superconducting magnets toforman essential part (6). HOCIO, < HOCIO, < HOCIO< HOC ‘of NMR spectrometer ? (©) HOCIO, Tit (0) Ma? > Mn+ (©) actinides (© Fe >Re © Curscue (@ transition elements 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work 86 _——<$mN —_ DP PI CC22 ‘5. Which one of the elements with the following outer orbital ‘configurations may exhibit the largest number of oxidation states? @ Sus! (35452 © 344s? @ 3a%4st 6 The catalytic activity of transition metals and their compounds is mainly due to (@) theie magnetic behaviour (©) their unfilled orbitals (©) theirabilty toadopt variable oxidation state (@) their chemical reactivity 7. Arrange Ce",La"?, Pm and Yb in increasing oder of their ionicradi. @ Yor I>m>Iv ( ieMemivon @ W>I>1ven “The value ofthe “spin only’ magnetic moment for one ofthe following configurations is 2.82 BM. The correct one is (@) Gin strong ligand field) (©) (in weak as well asin strong fields) (©) Gn weak ligand fields) (@ din strong ligand fields) In neutral or faintly alkaline medium, thiosulphate is ‘quantitatively oxidized by KMn0, to @ So, ) S02 © $0, @ so arke’s process is used (@) toextract Ag using NaCN () toextract Cu using CuFeS, (©) toextract Ag from argentiferrouslead (@ toextract Ag by forming amalgam ‘A metal which is not affected by conc. H;S0,,HNOs or alkalies forms an compound X This compound X can be used to givea complex which finds its application for tonning 17.@QO@ 18.@0@OO 2.@@O@ 23O@0OO 27.©©O@ SCN Gr 9.@@O@ 2W@OQO®@ 21. ©OO@ A@OOO 3OOQOO 2%. OOOO ‘Space for Rough Work 88. $A DP PI CC22 in photography. The metal is @ Au ® Ag © He @a 28. Ammonia forms the complex ion [(Cu(NH,,}* with copper ions in alkaline solutions but notin aciie solutions. What is the reason for it? (@)_Inacidic solutions protons coordinate with ammonia molecules forming NH; ionsand NH, molecules are not available (©) Inalkaline solutions insoluble Cu(OH),is precipitated hich is soluble in excess of any alkali (©) Copper hydroxide isan amphoteric substance 2. (@ In acidic solutions hydration protects copper ions ‘Ared sold is insoluble in wate, However it becomes soluble iff some KI is added to water. Heating the red solid in ates, tube results in liberation of some violet coloured furmes and droplets of a metal appear on the cooler parts of the test, tube, The red solid is @) Hel; © Pb,0, ©) HO @ (NH),Cr0, ). Four successive members ofthe first series ofthe transition metals are listed below. For which one of them the standard prtenil (Ey2jyq) value has postive sign? (@) CoZ=27) ) NiZ=28) © Cuz=29) @ FeZ=26) B@OOO YOOOO 3B».OOOO DAILY PRACTICE PROBLEM DPP CHAPTERWISE 2. Total Marks Correct Total Questions Attempted HEMISTRY Incorrect Net Score Cut-off Score 38 Qualifying Score 52 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time : End CHEMISTRY (cc23 ‘SYLLABUS : Coordination Compounds Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, 1 Which of the following is incorrect regarding 3 An example of doublesaltis spectrochemical series? (@) Bleaching powder (@) NH,>H,0 ) F>c,0F ©) Kal FCN] (© _NCS->SCN- (@) en>edta © Hypo (@_ Potash alum ‘Nickel (Z = 28) combines with uninegative monodentate ligand X- to form a paramagnetic complex [NiX,]>. The ‘number of unpaired electron(s) in the nickel and geometry 2 CggHlggCoN, 0, ,Pisthe formalae ofthe Cyanocobalamine, 4. (itamin B,.) it contain CN~ and CN is very poisonous, ‘than why this compound does not prove to be fatal for ‘us? (it inhibit the electron transport chain ? ofthis complex ion are, respectively: (@)_ CN" forms covalent bond (@) one, square planar () CN is coordinating tothe cobalt as the Tigand (©) two, square planar (©) CN hydrolysis immediately (©) one, tetrahedral (@ All of these (@ two,tetrahedral 1. @O0OO_2 @OOO_3. ©OOO_4 OOOO ‘Space for Rough Work £0. -A@$3a4_iI$Ii| i i i i PP C023 ‘5. The crystal field splitting energy for octahedral (Ao) and 10, Which ofthe following is organo-metallic compound ? tetrahedral (A) complexes is related as @ THY, & THOC HH), ® w & (© TWOCOCH), @ TWOCH), AL, Which isnot x- bonded complex ? ro canes (@) Zeise’s salt (b) Ferrocene (© Dibenzenechromiun —(@) Tetraethyl lead 6 —A-squareplanarcomplexisformed by hybridisation of which 12, A solution containing 2.675 g of CCl. 6 NH, (molar mass atomic enbitls? =261.5 g mol!)is passed through cation exchanger. The chloride ions obtained in solution were treated with excess © Per Prd ye of AgNOs to give 4.78 g of AgCl (molar mass = 1435 g © 8 PePyd2 © SPy-Prrdy ‘mol-!, The formula ofthe complexis : (At-mass of A= 1080) @ 5. Pp Py dye 7. Consider the following complex [Co(NH,),CO,|CIO, The coordination number, oxidation number, number of d- (@) [Co(NHs)6}Cg (6). [CoCI, (NH), C1 electrons and number of unpaired d-electrons on the metal (© [CoCI(NHs)5] — @_[CoCKNHS)51Clp are respectvel cone 13. Thetype ofisomerism present in Pentaminenitrochromium () 6.3.6.0 ©) 7.2.71 amass © 1164 @ 6.2.7.3 (@) optical (©) linkage 8 How many EDTA (ethylenediaminetetraacetic acid) (©) ionisation (polymerisation. molecules are required tomake an octahedral complex with 14, Red precipitate is obtained when ethanol solution of Ca? ion? dimethylglyoxime is added to ammoniacal Ni(II). Which of @ One ©) Two the following statements isnot true ? © sx (@ Three (@) Red complex has a square planar geometry 9. Which of the following are inner orbital complex (ie., (©) Complex has symmetrical H-bonding involving sp? hybridisation) and is paramagnetic in (©) Red.complexhas tetrahedral geometry. nature? (@) Dimethylglyoxime functions as bidentate ligand. (@)_ [Mn(CN)g]*, [Fe(CN) I, [ColC,04)5)- oH (b) [MnCig]*, (FeF}*, (CoF]> H,C—C=N~ (©) [Mn(CN)F>, (FelCN) timethylelyoxime = H,C—C=N (@) [MnCIg} , (Fe(CN),}*, [CofC,0,),]>- "OH Se > OOOO 6 @OO@ 7. ©OO@ 8 O©OO@ % OOOO 1.@QOO_U.@OOO_122.©OOO_13.©@OOO_14. ©OOO ‘Space for Rough Work GP_3371 DPP/ CC23 ———— tt 15, Amexcess of AgNO, is added to 100 mi of 20.01 Msolution of dichorotetraaquachromium (ii) chloride. The number of ‘moles of AgCl precipitated would be (@) 0002 () 0008 © oo @ 0001 16. Magnetic moment of Gd ion (Z= 64) is (@ 302BM &) 9.72BM © 798M (@) 10608M 17. Which of the following species represent the example of dsp? - hybridisation ? (@) [Fe(CN_)~ @) INKCN © [Ag(CN),1 (@ [CaCN),* 18. Which one of the following has largest number of (@) [IPR3).H(CON —(b) [Co(NH) C1” (© [RU(NH3)4CJ" —— @ (Colen),Ch,J* 1B, InFHCO), he Fe-C and posses (@ ioniecharacter (b) -character only (©) m-character (@) both o and x characters 20. the comet strstr of etylneamineetrancetic aid (EDTA)is HOOC 1 ct4- coon a DNC cH NCEE Hooc - Hc cit,-cooH Coot HoOC, N- CH, -CH, -Nt » HoOOc” HCH, COOH £00 a, LO, A N-CH-CHLN’ wr ENC, coon (@ HOOC-H, cH, 7 HOOC ‘The structure of which of the following chore species can be explained onthe basis of dsp? hybridization ? a. @ pack © Feit © coe @ Nice ‘The octahedral complex of a metal ion M?* with four monodentateligand,, >, and L, absorb wavelengths in the region of red, green, yellow and blue, respectively. ‘The increasing order of ligand strength ofthe four ligands @ WehCH,OH + Br (b) CHs-CH-CHy +H" — CH; ~CH-CH Br on © cHycH,on #2 5cH, =cHty @ (CHy)C-Br+ OH” —9(CH,),COH+ Br 6& Thereaction of CgHsN3CI- with CuCl gives @) CHCl ©) Colts (©) Cols ~ Cols @ CoH«Ch 7. On sulphonation of C,H,Cl (@)_m-Chlorobenzenesulphonic acid is formed (6) Benzenesulphonic acid is formed (©) 0-Chlorobenzenesulphonic acid is formed (@) 0-and p-Chlorobenzenesulphonic acid is formed ‘& —Thestructure ofthe major product formed in the following reaction CH ow DMF” is I cua on o cr ® cr io by } cue cH.ex © © ow I by 9. Which ofthe following will havea mesoisomer also? (@) 2,3 Dichloropentane (©) 2,3-Dichlorobutane (© 2-Chlorobutane (@)_ 2-Hydroxypropancic acid 10. The pesticide DDT slowly changes to (@) CC1,-CHO and chlorobenzene (©) p.p*Dichlorodiphenylethene (© p.p*Dichlorodiphenyldichloroethane (@ p,p*Dichlorodiphenyldichloroethene AL. o-Methoxybromobenzene is treated with sodamide and then with ammonia, The product formed is (@ oMethoxyaniline —— (b) Aniline (©) Methoxybenzene —(@)- m-Methoxyaniline 12. The starting substance for the preparation of iodoform is, any one ofthe following, except (@ CHjCHCOH)CH, —(&) CHjCH,OH (© HCH,OH @ CH;CocHs 13, Which of the following statements is wrong? (@) Ethyl chloride on reduction with Zn-Cu couple and. alcohol gives ethane. (©) The reaction of methyl magnesium bromide with acetone gives butanol-2. (©) Alkyl halides follow the following reactivity sequence ‘on reaction with alkenes. R-I>R-Br>R-C1>R-1 (@ C.H,C), may existin two isomeric forms 14, An organic compound A (C,H,CI) on reaction with Na/diethyl ether gives a hydrocarbon which on 'monochilorination gives only one chloro derivative, then A. (@) tert-butyl chloride (©) isobutyl chloride (©) sec-butyl chloride (@) n-butyl chloride 5. @QO@ 6 @OQO@ 1.@@O@ _U.@OO@ 7. @0©O@ & ©O0OOO % O0O@ 12.@@O@_13.©@OOO_14. @OOO ‘Space for Rough Work GP_3371 DPP/ C¢24 — iii el 15. Ifchloroformis left open in arin the presence of sunlight it gives (@) carbon tetrachloride (b) carbonyl chloride (©) mustard gas @) lewisite 16. The reaction oftoluene with Clp in presence of FeCl; gives "x and reaction in presence of light gives “Y" Thus, °X" and ‘Yar: (@) X=Benzal chloride, Y=0~Chlorotoluene () X=m-Chlorotoluene, Y= p~Chlorotoluene (© X=o-andp~Chlorotoluene, Y¥=Trichloromethylbenzene (@) X= Benzyl chloride, ¥ = m—Chlorotoluene 37. CHyBr+Nu—>CH3—Nu+Br- The decreasing ‘order of the rate ofthe above reaction with nucleophiles (Nw) AtoDis INU=(A)PhO™(B) AcO™ (©) HO”, (D) CHO") (a) A>B>C>D (b) B>D>C>A (© D>C>A>B @ D>C>B>A 18. The Wartz-Fittig reaction involves condensation of (@)_ twomolecules of aryl halides (b) onemolecule of each of aryl-halide and alkyl-halide (©) onemolecule of each ofaryl-halide and phenol (@)_twomolecules of aralkyl-halides. 19. ‘The major organic compound formed by the reaction of 1, 1, Ltichloroethane with silver powder is: 21, odoform can be prepared from all except (@) Ethyl methyl ketone (©) Isopropyl alcohol (©) 3-Methyl 2-butanone (@ Isobutyl alcohol 22, The reagent(s) for the following conversion, Br 2 . aN H H (@) alcoholic KOH (©) alcoholic KOH followed by NaNH, {© aqueous KOH followed by NaNH, @) ZvCHOH ‘Ina nucleophilic substitution reaction: R-Br+cr— PE 4k cls Br ‘hich one ofthe following undergoes complete inversion of coniguration? (@) CCUG HBr 0) CQHLCH,B © CHCHCHLBe Ge). CHGCCH,C HBr Chiorcbenzne reacts with tichloro acetaldehyde inthe eseice of HS, ° ll HO, cl+H-c-cc,——> 2 (a) Acetylene (>) Ethene Sa an ya ocean er eee a cH, a ® 6 HO OH I Resro 5.@OQO@ 16@OOO 17.©OOO 8.©OQOO 19.@O0OO@ fern 20.@OO@ _1-@OO@ 22.©0OO_3.©@OO_4. OOOO Space for Rough Work GP_3371 ed DPP/CC24 25, Benzene reacts with n-propyl chloride inthe presence of 28, Whats the product ofthe following reaction? anhydrous AICI, 0 give a (@) 3 ~Propyl1 ~chlorobenzene (b)_n-Propyibencene ccupns (©) Noreen SEN 2 (@)_Isopropylbenzene : 26, Replacement ofClofchlorobenzeneto give phenol requires __@)_N.N-timethyaniine drastic conditionsbut chlorine of 2 4-dinitroclorobenzene _() phenyllithium (CHgLi) (a) NOs makes ering lcwom ich at ortho and para) arachlro, Nima anne Seton * bs (@) metachloro-N.N-dimetyl aniline (0) NO, was fom meta pasion 28. Themajor produc formed whe I, 1, Ltichloropropaneis {© NO; donates eat mposition treated with aqueous poassiem hydroxide is 7 - a : (@ Propyne (b) L-Propanol (NO, withdraws € from ortho/para-psitions @ NO ean (©) 2-Propanol (d)_ Propionic acid 27. ‘Silver benzoate reacts with bromine to form 30, Consider the reactions coon © (cHy,cH- Higa CHO, (CHs)) CH -CH,OCyHs + HBr @ nan G_ (CHy)2CH-CHyBr—HO, (CHHy)CH~CH,OCaMs +B Goons “The mechanisms of reactions Gi) and (i) are respectively (@) Syl andsy2 ©) Syland yt 9 : © CoHsBr (© Sands? (@ Sy2andsyt 3.@OO@ 4@OOO 7.©OOO ¥%@OOO ». @OO@ 0.©@0OO PROBLEM DPP CHAPTERWISE 24 Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 37 Qualifying Score 54 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) Space for Rough Work DPP - Daily Practice Problems Chapter-wise Sheets Date Start Time : End ‘SYLLABUS : Alcohols, Phenols and Ethers Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. 1X INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, Lucas reagent is (@) Conc, HCland anhydrous ZnCl, (©) Cone. HNO, and hydrous ZnCl, (©) Conc. HCland hydrous ZnCl, (@)_ Conc. HNO, and anhyirous ZnCl Diethyl ether reacts, inspite ofits usual inert nature, with (@)_ Dilute suphuric acid (©) Dilute sodium hyeroxide (©) Boron trifluoride (@) Metallic sodium Vinyl carbinolis (@) HO-CH;-~CH=CH, (b) CHC(OH)= CH (© CHy-CH=CH-O# (® CH, -C(CH;0H) = CH, ‘Among the following compounds which ean be dehydrated very easily is cH, (@ CHCH,-C-—cH,cH, On on t (©) CH,CH,CH,CHCH, (© CH,CH,CH,CH,CH,OH (@ CH,CH,CHCH,CH,OH { cn rae @0OO_2 ©OOO_3. ©OOO_4. ©O0OO ‘Space for Rough Work £68 -_ $A DPR CC25, 5 a 8 (CH,CH,OH can be converted into CH,CHO by. (@) catalytic hydrogenation (©) eatment with LiAIH, (©) treatment with pyridinium chlorochromate (@ treatment with KMn Epichlorohyerin is, (@)3-Chloropropane (©) 3-Chloropropan-1-o1 (©) 3-Chloro-1, epoxypropane (@ None ofthese 2Phenylethanol may be prepared by the reaction of phenylmagnesium bromide with (@) HCHO ®) CHLCHO (©) CH,COCH, @ L\ HBr reacts with CH, = CH ~ OCH, under anhydrous conditions at room temperature to give (@) BrCH,~CH,-OCH, (©) H,C-CHBr—OCH, (©) CH,CHOand CH,Br (@)_ BrCH,CHOandCH,OH From amongst the following aleohols the one that would react fastest with cone. HC1 and anhydrous ZnCl, is (@) 2-Butanol (©) 2-Methylpropan- (©) 2-Methylpropano! (@1-Butanol 10. u. 2 3B. rr Which of the following cannot be made by using. Williamson's synthesis? (2) Methoxybenzene (©) Benzyl p-nitrophenyl ether (©) Methyl tertiary butyl ether (@ Ditert-buty ether Rectified spirits a mixture of (2) 95% ethyl alcohol + 5% water (b) 94% ethylaleohol + 4.53 water (©) 94.4% ethyl alcohol + 5.43% water (©) 95.87% ethyl alcohol + 4.13% water [Absolute alcohol (1009% alcohol is prepared by distiling rectified spirit over @ Na ©) Ger, © Me (©) MOC), Reagent used to convert allyl aleohol to acrolein is @ Mn0, © HO, (© 030, @ KMn0, In Williamson synthesis of mixed ether having a primary and a tertiary alkyl group if tertiary halide is used, then (2) Rate of reaction willbe slow due to slow cleavage of ccarbon-halogen bond. (©) Alkene willbe the main product (©) Simpleether will form instead of mixed ether. (@) Expected mixed ether will be formed. 5. @0@O@ 46 QOO@ 0.©0QOO@ _.©OOO 7. Q@QO® 8% @O0O@ 9% OOOO 12.©@©@OO 13.©@©OO_14. ©©OO@ ‘Space for Rough Work GP_3371 DPP/ CC25 ————— den 15. Arrange the following in increasing order oftheir acidity? 20. Williamson's synthesis is used to prepare ‘o-eresol(a), salicyeic acid), phenol) (@ c) CHMg! © m @a 17, When wine is putin ar, it becomes sour due to (@) bacteria (©) oxidation of ,H,0Ht0 CH,COOH © virus (@) formic acid formation 18, Osmium teraoxide isa reagent used for (@) hydroxylation of acetylenes (b) hydroxylation of olefins to give cis-diols (©) hydroxylation of olefins to form trans-diols (@)_ hydroxylation of carbonyl compounds 19. Sodium phenoxide when heated with CO, under pressure at 125°C yields product which on acetylation produces C “The major product C would be ‘9cocn, on COOH coc, @ o ‘CocH, oH ococh, ovo © OF © OD coon (@) acetone © PVC (©) diethyl ether (@) bakelite 21. Aspirin is an acetylation product of 6) pDiytontenzene (b) a Hydroxybenzoic acid (©) oDihydroxybenzene (© mien = Kylee ENS 4x The prod Ys (Pataca 0 opted (©, Phenol @)_o-Hydroxysulphonic acid Thefloing reaction 2nCh, ‘CHO; — (@) Peskin reaction (b) Gatterman-Koch Formylaton (©) Kolte's reaction (@ Gattermann reaction Denaturation of alcohol isthe (@)_ mixing of CuSO, (a foul smelling solid) and pyridine (Go give the colour) to make the commercial alcohol unfitfor drinking (©) mixing of CuSO, (to give the colour) and pyridine (a foul smelling solid) tomake thecommercalalobol unfit for drinking (© mixing of Cu(OAc), and ammonia to make the commercial alcohol unfit for drinking (@ mixing of Cu(OAc), and pyridine to make the ‘commercial alcohol unfit for drinking. re B@OO@ 16.@O@OO@ 1.@OQO@ BO©G@OO VY. @O0OO D 20.@OQO@_11.©OOO_2OOOO_23.@OQOO@_¥4. @OOO ‘Space for Rough Work GP_3371 [e-100 DPP/ CC25 2S, Formation of which compound given below from 27. Which one of the following sabtaens at por 6) CHLCHLCH CHB o ) CH,CH;CHACH=0 Cy © (CHCH,CH:CH:),0 chy ©) -0cH, @ ct,-cH,cn-cH, © coc, (ci What is Xin the following reaction ? 28. Williamson synthesis of ether is an example of (@) Nucleophilic addition oH OCH, (&) Eleetrophilic addition ° i! (©) Electrophilic substitution eae eee ee hile subs ae L We ols (@)_Nucleophilic substitution cH; cH; 29, Widespread deaths due to liquor poisoning occurs due to (@)_ presence of carbonic acd in liquor (a) CH;OH,H,S0, (@)_ presence of ethyl alcohol in liquor . (©) presence of methyl alcohol in liquor (©) CH,OH,CHO” Na (@)_ presence of lead compounds in liquor 30, Which ofthe following diols would cleave into two fragments (©) H,0/1,80, followed by CH,OH aoe (@) CH MgBr /etherfollowed by Hj0* (@) 1,3-hexanediol (©) 2,4-hexanediol (© 1,6hexanediol (@) 3,4-hexanediol B@OQOQD UOOOO 27.O@OOO B%OOOO %. OOOO 3#0.@QO@ DPP CHAPTERWISE 25 Total Questions Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 36 Qualifying Score 52 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work DPP - Daily Practice Problems Chapter-wise Sheets Max, Marks : 120 L Start Time : End CHEMISTRY (cc26 ‘SYLLABUS : Aldehydes, Ketones and Carboxylic acids Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Daly Practice Problem Sheet contains 30 MCQ's, For each question only one option is correct Darken the correct cicle/ bubble in the Response Grid provided on each page, TUPAC name of following will be Ho ct, 3 on 4 @ ® © @ 4-formyl3-methyl I-hydroxy benzene 4-formyl3-methyl phenol 4-hydroxy 2-methyl benzaldehyde 4-hydroxy 2-methyl carbaldehyde In which of the following, the number of carbon atoms does not remain same when carboxylic acid is obtained by oxidation @ cHRCOCH, ——&)CCACH,CHO © CH,CH,CH,OH — @ CH,CH,CHO Acetone oxime i obtained by reacting acetone with (NH, (o) NOH © NHN @ Ni.NI, Which alkene on ozonolysis gives CH,CH,CHO and CH;CCH, i on @ creme o cxcnar-crcy (@ CH -C=CHCH, cH (©) CH,CH,CH=CHCH, rT 1 @0OO_2 ©OO©O 3 @OOO_4 ©O©OO ‘Space for Rough Work Joc ‘3. Predict the prot inthe given reaction. CHO cl " oe + ow » om o “oo ‘on a CHOW CO on oH ‘The carboxyl functional group (~ COOH) is present in (@)_picricacid (b) barbituric acid (©) ascorbic acid (@ aspirin Which one of the following is reduced with zine and hydrochloric acid to give the corresponding hydrocarbon? (@) Acetamide (b) Acetic acid (©) Ethyl acetate (@) Butan-2-one Carboxylic acid group does not give the usual addition and elimination reactions of aldehydes and ketones because (@) O-Hbondis more poar than C=O group (b) carboxylate ion gets ionised (©) carboxylate ion gets stabilised by resonance (@) itexists as ~ COOH and theres no carbonyl group Phenyimethy Ketone can be converted into ethylbenzene 10, 2. 3. 4 DPP/ CC26 Inaset ofthe given reactions acetic acd yielded a product. CH,COOH + PCL, —+ A— Salle, ‘natch, CotisMatie ie Product C would be- CoHs I @) CHy-C(OMCgHy (0) CHsCH(OH)CrHs (©) CH;COCSHs (@CH CHOC Hs “An organic compound “Aon treatment wih NH, gives “B” ‘which on heating gives ‘CC when treated with Brin the presence of KOH produces ethylamine. Compound ‘A {@ CHCOOH (6) CH, CH,CH, COOH © cay-rcoon @) CHCH,COGH ot, Match the compounds given in List-l_ with List-lI and select the suitable option using the code given below: List List (A) Benzaldehyde @_Phenolphthalein @) Phthalicanhydride Gi) Benzoin condensation © Phenyl tensoute (D) Methyl salicylate Coae: A 8 © DM oo > w @ o® @ @ a) @ ow w w o oo 0 & w C4lsCH-CHCHO —®, CyH,CH-CHCH,OH Tihs above sequence X canbe (WN (0) Nabi, © Kicnout ——_@ Baheande) ‘Neeafehyde reacts with seoiarbaride and forms ctocurrie.Insricureis Go cic NNHCON-cHcH, Gi) Oil of wintergreen (iv) Fries rearrangement in oe tp by which ofthe following reagents? (b) CH,CH=NNHCONH, @) Lal, (Za-He HCl © cHscH=N—N—conn, (©) NaBH, (@ CH.Mgl ba @ ccH=N—cosHNN, PE = QHOO & OOOO 7. OOOO & GOOD % OOOO Gan 1.@O0OO _1.©OOO_2OOOO_B.©OOGOO_4. OOOO ‘Space for Rough Work GP_3371 DPP/ CC26 ——— htt 18. Which one of the following can be oxidised to the corre- sponding carbonyl compund? (@) 2-hydroxy-propane (©) Ortho-nitro-phenol (6) Phenol (@) 2-methyl-2hydroxy-propane 16, Benzoic acid may be converted to ethyl benzoate by reaction with: (@) Sodium ethoxide (b) Ethyl chloride (©) DryHC—C,H,0H (@) Ethanot 17. Heating mixture of sodium benzoate and soda-lime gives (a) benzene () methane (© sosiumphenoxide _(@) calcium benzoate 18, “Which ofthe fllowingcompoundss most reactive towards nucleophilic addition reactions? ° i @ cHy-C-H Q ©) cH -C-cH, 19. The increasing order of the rate of HCN addition to compound A~Dis (a) HCHO © PRCOCH, (@) DB>c © C>A>B @ C>B>A ‘The consituent of the powerful explosive RDX is formed during the nitration of (@) toluene ©) pheno! ©. glycerol @ uotropine CoHJC=N and CgligN2C exhibit which type of (@) Position (©) Functional (© Dextrisomerism —__(@) Position isomerism Which of the following reagents will convert -methylbenzenediazonium chloride into -cresol? (@ Cupowser —) 0 © Hyp, (© CHOH Replacementof -N'3CI™ from benzene dzonium chloride by iodine can be done by using @ ©) Nal © Pl; @ KI Which ofthe following compounds is most basic? DPP/ CC27 Hh. HCHO yx Nt yy sca Zin the above reacting sequence is @) CHsCHyCHNHCOCH () CH;CHCHNH (© CH,CH,CHCONHCH, @ cucH,cH,CoNHCoCH 12. Match the compounds given in List - I with their characteristic reactions given in List - IL Select the correct option List-1(Compounds) _ List-11 (Reactions) ()CH,CH,CH,CH,NH, 6) alkaline hydrolysis CH C=CH Gi) with KOH (alcohol and CHCl, produces bad smell @)CH,CH,COOCH, Gi) gives white ppt. with ammonical AgNO, () CH,CHCOFCH, (iv) with Lucas reagent cloudiness appears after $ minutes Options: o 2 w @ i G Gi) O o@ @ ww Gi © @ @ © Ww Ow wo Ww 13, Nitrosoamines (R,N ~ N = O) are insoluble in water. On heating with conc. H,SO,, they give secondary amines. The reaction is called (@) Liebermann nitroso reaction () tard reaction (©) Fries reaction (@ Perkin reaction 14, Allthreeamines 1°,2°,3° react with Ho 2 RX © Ory cons oma, Aes , Gicowp 1 @ 123 Response 5. @O©O@© 6 @OOG 7. @OO@ 8 @OOO % OOOO et .@©O@ 1.@OO©@ 2.©0O@ B.@OOO 14. @@O@ ‘Space for Rough Work GP_3371 DPP/ CC27 07 15. Which one of the following on reduction with lithium 20, The reduction of nitro compounds is most preferred in the 16. a. 18. 19. aluminium hydride yields a secondary amine? (@) Methyl isocyanide () Acetamide (© Methyl cyanide @ Niroethane Aniline reacts with phosgene and KOH to form on ° the sticoct sco © ® When aniline reacts with oil of bitter almonds (C@HlsCHO) condensation takes place and benzal derivatives formed. Tis is known as {@) Million’sbase (6) Schiff'sreagent (© Schifts base (@)_Benediers reagent Which reaction sequence would be best to prepare 3-chloroanine fom benzene ? (@) Chlorination nitration, reduction (©) Nitraton, chlorination, reduction (©) Nivraton, redvtion, chlorination (@ Nitration, reduction, acetylation, chlorination, hydrolysis Anita alkane eacts with HONO to give insoluble product inalkal which turns biueon treatment with an alkali. The niteoalkaneis © CH;CH:NO, ©) CHy—CH-CHNO» CH (© (CH),CHNOy (@ (CH)3CNO2 presence of (@) Pa/H, in ethanol (©) finely divided Ni (&) Sn+HCL (@) iron serap and HCL 21, Ethyl isocyanide on hydrolysis in acidie medium generates (@) propanoic acid and ammonium salt () ethanoic acid and ammonium salt (©) methylamine salt and ethanoie acid (@ ethylamine salt and methanoie acid ‘Acetamide is treated with the following reagents separately. ‘Which one ofthese would yield methylamine? (@) NsOH-Br, — () Sodalime (©) Hotcone. H,S0, () PO, 23, Match he compounds in Lis I with theirnatare from List I as seen in aqueous medi Listt List L_Acetamide A. Acidic IL Benzonitile B. Basic TL Tietylanine © Neutra 1. Phenol @) ECILC\M-B:IV-A () L-B:I-C:IILC.IV-A © ECILBAI-BIV-C (@ L-A;I-A;IIEC:IV-B 24, The crrect order of basics ofthe following compounds au cc CH,—CH,—NH, vu, 1 2 ° (chy .NH cH—C—Ni, 3 4 (@ 2>1>3>4 © 3>1>2>4 @ 1>2>3>4 () 1>3>2>4 reer ery 1.@QO@ 16.@O0O@ 20.@OO@_11-@OO@ 17.@QOO@ B@OQO@ 19.@OOO@ 22.©©0OO_23.©0OO_4. OOOO ‘Space for Rough Work GP_3371 e4.08|]@-—$£@2———_§£_ —_—_——______________ DPP/ CC27 25. Which ofthe following reactions will not give a primary (@) CH,CONH , —82/K0H_, (b) CH. nen EA, © cance, @ 26 Indicate which nttogen compound amongst the following ‘ould undergo Hoffa reaction (ie. eaction vith Bry tndstong KOH) tofumish the primary amine (R- NH) (@) RCONHCH, (6) RCOONH, © ROONH, ——(@ R-CO-NHOH 27, tn he easton CltgNH, +C8, —#O2-> he pat obtained is (a) phenyl isocyanide (©) p-amino benzene sulphonic acid 28 Reagents capable of converting cyclohexanone to Nel eydohensfanines 3 2CHy (©) phenyl cyanide (@)_ phenyl isothiocyanate cutjconnty —UAHe, 2. 25. 7 2%6.@OO@O 27.©OOO 2%.@O0O@ (@) CHsCHpBr and NH (©) CH,CH,NH, and H, /Pt (©) CH,CH = 0 and NH (@ LiAIH, followed by HO and then CH3CH,Br ‘The intermediate obtained inthe following reaction () R-N=C=0 (@) None of these (© Bosh (a and) Which ofthe following gives propylamine upon hydrolysis? (@) CH,CH,C=N (©) (CH3CH,CH,)2NH ° (© CHy ~C ~ NHCH,CH,CH, (@ CH,CH, - CH= NH 29. @©@O@ DPP CHAPTERWISE 27 - CHEMISTRY Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 36 Qualifying Score 52 Success Gap = Net Score ~ Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work DPP - Daily Practice Problems Chapter-wise Sheets Start Time : End Max, Marks : 120 CHEMISTRY (cc2s ‘SYLLABUS : Biomolecules Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Daly Practice Problem Sheet contains 30 MCQ's, For each question only one option is correct Darken the correct cicle/ bubble in the Response Grid provided on each page, 1. Threeyelicstructues of monosaccharides are given below 2, Which of the following statements about vitamin By, is “which ofthese are anomers HW ‘on | Ho: un] i on} ‘on | HO Ho- Hu? Ho: HG HO i on H on | # on h i Ho H cH,oH cHoH CHOH © @ ap @ andl () Mando (© Tandit (@)_ Mlisanomer of fand 1 3 incorrect ? (@)_Tehas acobalt atom (@)_Iralso occurs in plants (©) Itisalsopresentin rain water (@) Itisneeded for human body in very small amounts Proteins when heated with cone. HNO, givea yellow colour. (@) Oxidizing est (©) Xamthoproteic test (©) Hoppe’s test (@) Acid base test ‘The change in the optical rotation (with time) of freshly prepared solution of sugar is known as (@) Specific rotation (©) Inversion (©) Rotatory motion (@ Motarotation 1 @©OO _2 @OOO_3_ ©OOO_4 OOOO ‘Space for Rough Work 14100} $< _———___—___ DPP/ CC28 5 2 ‘Table sugarisa (@) disaccharide of d-glucose and d-fructose (©) amonosaecharide © ad (@) D-glucose ‘The pair of compounds in which both the compounds give positive test with Tollen’s eagentis (@) Glucose and Sucrose (b) Fructose and Sucrose (© Acetophenone and Hexanal @ Glucose and Fructose Hydrolysis of sucrose i called (@) hydration ©) saponi (© esterification ©) inversion ‘Which is nota true statement? ride containing two glucose units tion (@) a carbon of a-amino acid is asymmetric (©) all proteins ae found in L-form (©) human body can synthesize all proteins they need (@) at pH=7 both amino acids and carboxylic groups exist inthe ionised form ‘The bes solvent for removing bute stain from cloth is @ CHO, ©) CHLOH © CHOC H, @ HO 10. nL. 2. 3B. 4 ‘The number of amino acids found in proteins that a human, body can synthesize is @ » @ 10 os ou Chemically amylose is a _ ‘o-D-(4}-glucose units held by (@) long unbranched chain, C1-C6. () branched chain, CI Ce. (©) long unbranched chain, C1-C4, (@) branched chain, CI-C6 Which is wrongly matched? (@) Insulin - steroid hormone (©) Estrone control the uterine eycle in women (©) Oxytocin - contraction of uterus (@) Pot. metabisulphite - food preservative If one strand of DNA has the sequence ATGCTTGA, the sequence in the complimentary strand would be (@ TACGAACT () TOCGAACT © TacGTACT (@ TACGTAGT In nucleic acids, the sequence is (@) phosphate - base - sugar () sugar- base-phosphate (©) base- sugar - phosphate (©) base. phosphate - sugar with 200-1000 _lycosidc linkage 5. @©O@ 6 @OO@ 10.@0O@_1.@O0O@ 7. @0O@ % @OQOO@ % Q0@O@ 12.@@©@ 13.@@O@_14. @OOO ‘Space for Rough Work GP_3371 DPP/ C¢28 —_A Roa sei 15. Which statement is incorrect about peptide bond? (a) C-N bond length in proteins is longer than usual C-N ‘bond length () Spectroscopic analysis shows planar structure of =C-NH- bond t é (©) C-Nbond length in proteins is smaller than usual C-N ‘bond length (@) None of these 16. Anacidic aminoacid among the following is (@)_ glycine (©) valine (©) proline (@ leucine 17. Inan amino acid, the carboxyl group ionises at PK y, =2.34 and ammonium ion at PK, =9.60. The isoelectric point of| (a) aketohexose (b) analdohexose (©) ano-furanose @ an epyranose ‘A reagent suitable for the determination of N-terminal residue of a peptide is (@)_ p-Toluenesulphonyl chloride (©) 2,4-Dinitrophenyinydrazine (©) Carboxypeptidase @ 2,4-Dinitroflorobenzene 21, Amino acids generally exis inthe form of Zwitter ions. This ‘means they contain (@)_basic—NH, group and acidic COOH group (©) thebasio— RI, group and scidic COO" group (©) basio—Ni and acidic group the aminoacid isat pH (@) basie-COO™ group and aciie— Si group @) 57 (b) 234 22. ‘The two functional; 9s present in a typical carbohydrate ©) 960 @ 697 are srowps aa a 18, Forosizonefomatontheeiativesrucuralunitnecesayis Cy _cHoand COOH @ — CHOCH, ©) chon () >C=0and-o1 jf ; bo bo © —Ofland CHO q q (@) -OHand—COOH 23, Enzymes are eset as bioeatalyss, They function in (© CH,OH @ CHO (a) aqueous medium, temp = 30-35%; pH=7 4 - () organic medium cuioctts Guioctis (2 spon meander enene pl condos (@ Nome of these 19, ‘Thefolowing earbohyrateis peace i {DNA = (b) RNA 6. © iia Ho “arbohydrates oa ou (@) Carbohycrat 4 ‘on 4 " ae E.@OO@ OOOO 17.@O0OO 8%OQOOO VY. @OOO EE 2.000 2.9000 2OOOO_2B.O0OO_4. OO©OO ‘Space for Rough Work long DPP/ CC28 25. Lack of essential amino acids inthe diet leads tothe disease 28, Identify the correct statement regarding enzymes called () Night blindness (b) Pernicious anaemia (©) Kwashiorkor (@ Sickel cell anaemia 26, Which of the following structures represents thymine ? (@) enzymes are specific biological catalysts that cannot be poisoned (b) enzymes are normally heterogeneous catalysts that are very specific in their action (©) enzymes are specific biological catalysts that can ° yH ‘normaly fanction at very high temperatures ((1000K) any x4 (@ enzymes are specifi biological catalysts that possess welldefined active ites ® A A 28, into DNA and RNA tery sand phos 1" H ester linkages are at— on (@) Cy and C, respectively ofthe sugar molecule . tee (b) C; and Cy respectively ofthe sugar molecule ® “y (©, Cy and Cy respectively ofthe sugar molecule Ho’ SN’ (@) Cs and C; respectively of the sugar molecule 30, Glucose molecule reacts with X number of molecules of phenylhydrazine to yield osazone. The value of X is (@) three ©) two (© one © four 27. ‘The segment of DNA which acts as the instrumental manual for the synthesis ofthe protein is: () ribose () gene (©) nucleoside (@) nucleotide LSE 2-©Q0OOQ %O©OOO 277.@OOO BOOOO % OOOO i #.@OQOO ANT eyed (01-0) =) 0/8 Al AAS aoe SO Total Questions Total Marks Attempted Correct Incorrect Net Score Cut-off Score 37 Qualifying Score 56 Success Gap = Net Score — Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Max, Marks : 120 L Start Time : End Time : CHEMISTRY (cc29 SYLLABUS : Polymers. Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Dally Practice Problem Sheet contains 30 MCO's. For each question only one option is corect Darken the correct cicle/ bubble in the Response Grid provided on each page, Which ofthe following compound is used for preparation 2 Which one of the following is not an example of chain ‘of melamine formaldehyde polymer ? @ © NA ‘NH, x 3 BN yh ni, i Ss 4 _ a | 7 : a NH ‘growth polymer? {@) Neoprene (©) Banas (©) PMMA (@) Giyptal Urethane is © H,N-C=N — @ HAN-C-On ° © HO-CeN — @ H.N-C-OCyHy ° The turbidity ofa polymer solution measures (@) the light scattered by solution () the light absorbed by a solution (©) the light transmitted by a solution (@ None of these 1 ODOO _2 OOOO _3. ©OOO _4 OOO ‘Space for Rough Work fo114 5. Which of the following polymers do not involve cross linkages? (a), Melmac () Bakelite (©) Polythene (@) Valeanised rubber 6& Which compound/set of compounds is used in the ‘manufacture of nylon 6? (6) HOOCICH,,COOH + NHL(CH),NH, cH Hl (© CH, =CH-C=CH, ° (@) natural rubber (b) synthetic rubber (©) highly vulcanized rubber (@) polypropene cH; & Monomerof} -G—cH- | is ¢-CHa CH; (@) 2Methylpropene —__(b) Styrene (©) Propylene (@ Ethene 9 Caprotactam polymerises to give (@) terylene () teflon (©) slyptal @ Nylons 10. Polymer used in bullet proof glass is (@) PMMA () Lean (©) Namex @ Kevlar L,_ Structures of some common polymers are given. Which one is mot correctly presented? DPP/ CC29 ( \ Hee ogre 4 (b) Terylene; c0e-(6)-conc 0-0 (©) Nylon 66; [-NHCH»gNHCOXCH,CO-], (8) Teflon; (-CF~CR.)y 12, Which one ofthe following sets forms the biodegradable polymer? @) CH, =CH-CN and CH,=CH-CH=CH, () H.N-CH,~COOH and H,N-(CH,),~COOH (© HO-CH,~CH,-OH and =O 13, Which of the following catalyst is used in preparation of high density polythene ? (@)_ Peroxide catalyst () Ziegler - Natta catalyst (©) Wilkinson's catalyst (@ Pa- catalyst 14, Whichis the monomer of Neoprene inthe following ? (@) CH; =¢—CH= cH CHS cH, =¢—cH= cH a © CH,=cH— (@ CH,=CH—CH=CH, mS. OOOO 6 OOOO Gre W.@0OO@ _1.©OO@ 7. @©O@ §% @O©OO % QO0OO 12.@@OO_B.©O@OO_4. OOOO ‘Space for Rough Work GP_3371 DPP/ CC29 15. 16. 7. 18. 1. ‘Buna-N synthetic rubber is a copolymer of (@) H,C=CH-CH=CH, and H,C,—CH=CH, (b) H,C=CH-CN and H,C=CH-CH=CH, (© HyC=CH-CNand H.C = CH-C = CH, 1 CH; a l (@ HC=CH-C=CHy and HxC = CH-CH =CH, ‘The polymer containing strong intermolecular forces e-, hydrogen bonding, is @) teflon () nylon 6,6 (©) polystyrene (@ natural rubber Formation of polyethylene from calcium carbide takes place as follows aC +2H0-—> Ca(OH), + CoH (CoH; +Hy —>CoHy nC Hy —(-CH2 ~CH>~)q ‘Theamount of polyethylene obtained from 64.1 kg of CaC, is (@ The () 14kg (©) 21kg (@) kg Ziegler-Natta catalyst is (@) KIPCIS(C2H.)]——_(b)_(Ph3P)jRHCI (© ALCHs)g+TIC, — @) FE(CSHs)y [Nylon 6,6is a polyamide obtained bythe reaction of (@) COOH(CH,), COOH + NH,C,H,NH, (©) COOH(CH,), COOH + NH, (CH,),NH, (©) COOH (CH,),COOH+NH, (CH.,), NH, (@)_ COOHC,H, COOH) + NH, (CH,),NH, ‘Which one of the following monomers gives the polymer a. jor151 Which compound/set of compounds is used in the manufacture of nylon-6,6? (@) HOOC(CH),COOH + H.N(CH),NH, () CH,=CHC(CH)=CH, (© CH=CH, — Which ofthe following is not correctly matched? (8) Neoprene CH — C = CH-CH, ~ a l, f i i (©) Terylene; |-OCH,—cH,—0-¢ cH; I @ PMMA: TCH -¢ coocH, Plexiglas (PMMA) isa polymer of @) acrylicacid () methyl acrylate (©) methyl methacrylate (@) None of these neoprene on polymerization? ee a 6) styrene @ CCl, =Ccl, © cH = ¢-cH=cH, ©) sartsonee © CR=CR @ CH) =CHCI @) acrylonitrile PE 5 OOOO 16OO0O 17.0000 60000 OOOO BEE 2-000 2.0000 _2OO0OO_2BOOOO 4. OOOO ‘Space for Rough Work e406/_<$@$@—___——_———___________ ppP/ C29 5. Synthetic human hair wigs are made from a copolymer of 28. Which of the following structures represents neoprene Jnyl chloride and acrylonitrile ands called polymer? @ PVC (b) Polyacrylonitrle (@ (CH)~ C=CH-CH,),, (©) Cellulose (@ Dynel I 26. Melamine plastic crockery isa codensation polymer of| a @) HCHOand melamine () HCHO and ethylene CN (©) melamine and ethylene (€) None of these 1 27. Match List-I (Monomer) with List It Polymer) and select () (CH)~ CH}, the correct answer using the codes given below the lists List Listit 1 Hexamethylenediamine A. Bakelite TL Phenol B. Dacron MI, Phthalic acid C.Glyptal IN. Terephthalicacid D. Melamine @ «CH-CH), E.Nylon I Cols (©) FE IFA TLC VB (@ ED.ILCMIFA,IV-B- 30, Which one of the following is used to make ‘non-stick’ 28. Among cellulose, poly (vinyl chloride), nylon and natural cookware’? rubber, the polymer in which the intermolecular force of (a) PVC. attraction is weakest is () Polystyrene (@)_ nylon (b) poly vinyl chloride) () Poly (ethylene terephthalate) (©) cellulose (@) natural Rubber (© Polytetrafluoroethylene PIE 25.OOOO %OOOO 7.OOOO %OOGO ¥. DOGS BE 3.9000 Aa ae 60S TP earned ass Total Questions 30 Total Marks 120 Attempted Correct Incorrect Net Score Cut-off Score 38 Qualifying Score 57 Success Gap = Net Score - Qualifying Score Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 DPP - Daily Practice Problems Chapter-wise Sheets Date: Start Time = End Time : CHEMISTRY (cc30 ‘SYLLABUS : Chemistry in Everyday Life Max, Marks : 120 Marking Scheme : + 4 for correct & (1) for incorrect Time : 60 min. INSTRUCTIONS : This Daly Practice Problem Sheet contains 30 MCQ's, For each question only one option is correct Darken the correct cicle/ bubble in the Response Grid provided on each page, 1 Thedng 4 is used as cHNH, Ms N « ® ) 7 CH H ‘OH 1 on ou cH, —NH, CH,CHLNH, CH, CCH (@) Antacid (b) Analgesic La (©) Antimicrobial (qd) Antiseptic © @ - 2 Parkinson's disease is linked to abnormalities in the levels of OH ‘OH dopamine in the body. The structure of dopamine is oe on 1. @0OO_2 @O@OO@ ‘Space for Rough Work 7. Which of the following ceramics possesses good strength, translucency and very low porosity (@) whiteware () earthenware (©) stoneware (@)_ bricks and tiles Io-119] DPP/ CC30 3. The corect structure ofthe drug paracetamol is & Which one ofthe following is employed as a tranuilizer on on drug? (@) Promethazine (&) Valium a Oo (©. Naproxen (©) Mitepristone 9. Which ofthe following substances cannot be used as Youu: cnc fixatvein perfumes? 2 NHCOCH, (@) Benzoin a a (b) Sandalwood (© Glycesdinitate © 7 (@ Gityery diacetate 10, Detergents are prepared by the action of H,$0, followed bonn, boc, bynevtralizaton by starting with 4. Arsenic drugs are mainly used inthe reacmenc of (@) chloesterol (by lauryl alcohol (@) Jaundice ©) Typhoid (&) cyclohexanol @ prnitrophenol a © ea on (@) Cholera 11. Which of the following is not correctly matched? “Antseticchloroxyenol is Seren anes a (a) 4-chloro-3, 5-dimethylphenol eee Recepte Ee ee exaeas eal «ruil to bodys communication (©, -chloro-2 5-dimethyiphenol proces. {@) S-chlor-3,4-dimethyphenol Drugsthatmimic = Antagonists 6 Thefollowing compound is used as the natural messenger by switching on the receptor. o-€-cH, Drugs that binds to ~ Agonists the receptor site and inhiit on its natural function (@ anancinflammatory compound (@) Gidonly (©) Giijonly (b) analgesic (© Gand diy (© dandGiy (©) hypnotic 12. Commonly used antiseptic Det is a minture of (@. antiseptic (©) o-chorophenoayenol + terpeneol (©) o-cresol + terpeneol (©) phenol +-terpeneol (@ ehloroxylenol + terpeneol an 8 @OQO@_ 9 ©O0O@ 3 @OOO 4 ©OOGs. OOOO 10.©©O©@ 6 @0@O@ 7. ©OO@ 1.@@QOO_ 2. @OOO ‘Space for Rough Work GP_3371 DPP/ CC30 —_ AS a_i Hit B. 14. 15, 16. 1. 18, 9. Which one ofthe following can possibly be used as analgesic ‘without causing addiction and mood modification ? (@) Diazepam (&) Morphine (©) N-Acetyl-para-aminophenol (@) Tetrahydrocannabinol ‘The indicator used in the titration of a strong acid and a strong base is (@) phenolphthalein (©) alizarin yellow Benzalkonium chloride isa (@) cationic surfactant and antiseptic (B) anionic surfactant and soluble in most of organie solvents cationic surfactant and insoluble in most of organic solvents (@ cationic surfactant and antimalarial During the deepening ofthe colour of a dye, the absorption shifts towards red. This shifting is called (a) bathochromie shift (b) hypsochromic shift (©) hyperchromicshif —_@) auxochromieshift Amonillin is semi-synthetic modification of. (@) penicillin () streptomycin (©) tetracycline (@ chloramphenicot ‘Select the incorrect statement, (@) Equanilis used to control depression and hy (b) Mifepristone is synthetic steroid used as “morning afer il (0.2 percent solution of phenol is an antiseptic while its LO percent solution isa disinfectant. ‘A drug which kills the organism in the body is called bacteriostatic Antibiotics that are effective mainly against Gram-positive ‘or Gram-negative bacteria X. Antibiotics tha are effective against single organism or disease are Y ‘What isX and ¥? () methylorange (© redlitmus. © © @ a. @ road spectrum antibiotics. Y = Narrow spectrum antibiotics. (b)-X=Broad spectrum antibiotics. imited spectrum antibiotics (©) X= Narrow spectrum antibiotics. imited spectrum antibiotics. (@)_X-= Narrow spectrum antibiotics. YY =Broad spectrum antibiotics, Structurally biodegradable detergent should contain (@) mormalalkyl chain (b) branched alkyl eh (© phenyl side chain @) eyclohexyl side chain H, — Receptor antagonists is aterm associated with (a) Antisepties () Anthistamins (©) Antacids (@ Analgesics Which ofthe following isnot rue ? (@) Some disinfectants can be used as antiseptics (b) Sulphadiazine isa synthetic antibacterial (©) Aspirin is analgesicas well as antipyretic (@ Polystyrene is used to make non-stick cookware ‘Which ofthe followings forms the base of talcum powder? (@) Zine stearate (©) Sodium aluminium siicate (©) Magnesium hydrosilicate (® Chalk “The structure given below is known as sete i i Hs: cH, Orov-bord Toke, J oF iH mmr B.@OQO@ 14.@O@OO@ B.@QO@ Y.@OQO@ 23.@@0O@ A@OOO Sa Gr 15.@@OO 20.@OOO 1.@O©O@ 2 @OOO@ 6.@OQO@ 17.@@O@ ‘Space for Rough Work 1e120- $$ DPP/ CC30 25, Most of the deodorants contain aluminium salts because they (@) acts antiperspirants (©) actas anti-bacterial agents (©) mask body odour @) Allthe these 26, Chemical substances used by insects for communication recalled (@) pheromones ©) hormones (©) enzymes (@ nucleoproteins 27. Antseptcs and disinfectants either kill or prevent growth of microorganisms. Identify which of the following statements isnot true: (@) Chlorine and iodine are used as trong disinfectants (©) Dilute solutions of Boric acid and Hydrogen Peroxide ate strong antiseptic 29. (©) Disinfectants harm the living tissues. (@ 0.2% solution of phenol isan antiseptic while 1% solution acts as a disinfectant ‘The substance which is not an artificial sweetener (@) sueralose () alitame (©) saccharin (@ sucrose ‘An antibiotic witha broad spectrum. @)_Killsthe antibodies (b) acts on a specific antigen (©) acts on different antigens (@ acts on both the antigens and antibodies SLY -3uses__propellants (@) solid (0) liquid (©) solid-tiquid (@) biliguia ¥#.@OQO@ Total Questions B.@OO@Q %@O@OOO 27.©O0OO B%@OOO »%. @©OO@ Lea sake OaL Ailsa S0) 5191) pd oe La ll Dd OLS Attempted Incorrect Cut-off Score Qualifying Score Success Gap = Net Score - Qualifying Score | Net Score = (Correct x 4) - (Incorrect x 1) ‘Space for Rough Work GP_3371 CHEMISTRY SOLUTIONS DAILY PRACTICE PROBLEMS deck L (©) 6.023% 103-1 mole Wein ‘Thus 6023 x10 =0.1 mole 2) Notmoet= Fett WoghotNy 01282 28¢ (© Weightofsilver=0.1 g No.of moles in 200mg = 99,44 (@)_ Weight of oxygen = 32% 0.1=3.2¢ 5x 10-? moles 8. (@ Mole of Mg,(PO,), contains 8 mole of oxygen atoms No. ofmoles in 10?! molecules mole ofonygen ioms= | mole ofMg,(PO,), mole of Mg (P04), = 1 = 1.6710 motes 60210 (025 male of oxygen atom = + 0,25 mole of MgyPO,), Novof moles lt=(45—1,67)x 10° =2.88 10° 3 3 @) 2BCy +34, 28+ 6c = 3:25.10 mole of Mg;(PO,), 3 10. @Sincemoavty of solutions 3.60M. means 3.6moles oe BCL, +34 B+3HC1 Of HS is present in ts I ite solution ‘Mass of 3.6 moles of H,S0, ‘Now, since 10.8 gm boron requires hydrogen Rete =3-224Lanne =36x98 g=352.8 2 1000 ml solution has 352.8 g of SO, hence 21.6 gm boron requires hydrogen Given that 29 of SO, is presenti = 100 gof solution 3.224 ob anne. 352.8 gofH,S0, ispresentin 2 108 100 359.8 of s 4. (©) M.Wrof Na,SO,.10H,Ois 322g which contains 224 g ag *3528 g of solution ‘oxygen. ~. 32.2 g will contain 22.4 g oxygen. = 1216 g of solution 602x10™ Mass _ 1216 5) Moles ofurea present in 100ml of sol = ©22*10— Density = Mass_ _ 7216 122 git » Li 6.0210 = Volume ~ 1000 Ls 10 AM _ Be = 0221071000 _ 1x4 1, ) From b= 2 6.0210 «100 io [ss M= Moles of solute present in IL of solution} ¥jx640 _ 620%:300 6 @ Relatveatomie mass= eran” 27342) “Mass of one atom of the element 1/12" pant of the mass of one atom of Carbon ~12 ‘or Mass of one atom ofthe element | 2 @ ‘mass of one atom of the C—12 Now if we use 7 in place of the formula becomes, Number of atoms of ron = 22476 56 13. (@) 20volume H,O, means that Lm ofthis H,O, solutions Relative atomic mass = Mass of one atom of element produces 20'ml-of O, at NTP. on decompesition by "Mass of one atom of carbon heat Relative atomic mass decreas twice For 20 ml. of Othe volume of 20 volume H,0, 7. (©) NaCl + HyS0, —>NaHSO,+ etd ee eae Nao For { mL of ,,the volume of20 volume According to law of conservation of mass. "mass is neither created nor destroyed during a chemical change" For 5000 mLor SL of Othe volume of 20 ‘Mass of the reactants = Mass of products 1, er o= eeenians volume H,0, required= =F 5000 mL, =250 ml. or x =2925¢ 14. (@)2Al(8) + HCI(ag) > 2ALP*(ag) + 6CI (aq) +3H(g) 8. (© (@)_ WeightofH,=mole x molecular wt ‘6 moles of HCI produces = 3 moles of H, =3x 224 Lof H, atS.TP 1382 -— ———————————_—__—_ DP P/ C01 18. @ 16. © 17. @ 18. © 122.4 6 * 1 mole of HCI produces = of Hat STP 1.2 Lof H, at STP 95% H,SO, by weight means 100g H,SO, solution ‘contains 95g H,SO, by mass Molar mass of HS, = 98g mol L Moles in 95g = % 969 mole 98 Volume of 100g H,S0, 100g 1834 om ‘mass vw @ ensity = 54,52 em} = 54.52 x 103 L Moles of solute Volme of solute in L __0969 “3452107 50 ml of 16.9% solution of AgNO Molarity = 78M 45 gof AgNO, 845e (078414 16%3) g/mol =00497 moles 50m of 5.8% solution of NaCl contain 845g 20. @) 169.8g/ mol 58.69) 38 )-204 29% (23 +35.5)g/ mol bor) ‘AgNO,+ NaCl > AgCl+Nao+clo Tinole 1mole mole 0.049 mote 049mle 0049 moleot w bo 21. fa) = Ew = loqgq)Molecla Mase = (01049) «(107.8 +355) meee) 2. Number of valence eleetronsin aN ion Now, 1 molor42 of N; has = 6.023 x 1023ions 0,42 got Nj has 6.023 <4 x 10% valencee™ = pas 6.023%1%10" 5 1 got Nj has 8023210" tence e amie! 42 3 42 gof Nj has 42*602341410" ence e-ie, 2 OLIN, valence e~ 74.15% of chlorine means 74.75g chlorine is present in 100g of metal chloride ‘Weight of metal = 100g - 74.752 =2525g B@ Equivalent weight ht of metal ~ weight of ehlorine 2525 7475 X355 4355 PR 2evp. Equivalent wt. of metal +35.5 26948 T2353 Formula of compound = MCI, "18 gm.thOconains-2gmHl O72 gm F,Ocontans Valeney of metal 2 2072 gm is078 444 gm CO, contains = 12,gmC :, 308 gm CO, contains 08 gmHt 2 Far 308= 084 gmC ‘Empirical formula NajCOs¢2HCI—+2NUCI+ 0 +CO, NaHCO +HCI—>NaCI+ H,0+C0, 1Na,CO, + NaHCO, + NaCl + HCL —> 48g Ag Bg (excess) al Tig washngsods —+ 8C0, + CO, fromNs;C0; fomNsHicos ‘Thus, on complete reaction with HCI, Lkg of washing soda will evolve 9 mol of CO;, 2.6 has two significant figures. (0.260 has three significant figures. 0.002600 has four significant figures. 2.6000 has five significant figures. Given mass of solute (w) -mass of solvent (9) 20.8 1000g ‘Mol. mass of solute = 60 ¢ Liz g/ml density of solution From the given data, Mass of solution Mol, mass Volume ofsolation y = 1120 12 Ww. ‘Mol mass>V( In an unknown compounds containing N and H given % of H= 12.5% 6 ofN = 100-125 =87.5% ‘Now molarity (M) GP_3371 DPP/ CCO04 — i ss Element | Percentage H 125% N 875 *, Molecular formula ofthe compound will be =(NH,), = NH 24 @ Bach + 1:0, —> BaS0,! + 2HCL mes mee mse oe nue 5. €) SCO 105 5C03 +13 254 Moss of 05 = 224 =001 = 005molesof CO Weightot O05 28-14 Weight CO; =2-14=068 Hence of COy as anRT 2. 56x 008214273, PVenRT 3 Soxt= 2S M.Wt=30.12 Hence gas is NO. ‘The required equation is 2KMn0 4 +3H350,—> K,S0, +2MnS04 +3H;0+5[0] nascent oxygen 2Fe(C04)+3H,S0, +3[0]—> Fe3(S04)3+2CO, +3H,0 21. @) 2B. 29, @ 30. © {O} required for 1 mol, of Fe(C,0,) is 1.5, 5 (0] are obtained from 2 moles of KMn0, 1.5 (O] will be obtained from = 2415-06 motesofKMn0, GH, +30, —> 20, +2H,0 de 96g +» 2B gol CoH, undergo complete combustion by 6 3010, 2.8kg of C,H, undergo complete combustion by =9.6kg0fOy, C3Hly +50, -»3C0, +4410 a 3a catty + 305-9405 458450 G-a 4G-a) But,3a-4(3—a)=10 ‘ (Propane )and3-2=1 (Butane ) Hlement | % Simplest ratio of atoms © [93 41274=15 Hf eae 6M2T=25 0 [sas Empirical formula =C,H,0, ‘Empirical formula mass 3 x 12) + (5x1) +(2x16)=36+5+32 Molecular mass = 2 Vapour density =2x7; molecular mass Empirical formula x2 = (CyH,0,)x2=C,Hi,, CHEMISTRY DAILY PRACTICE PROBLEMS SOLUTIONS Perry 1. (©) Thespecies CO, NO*,CN- and? contain 14electrons wn? n 109672.76 gg 2 Nac: NoofeinNat = ALNovofNe-t ‘The ne Belongs to Paschen series =11-1=10 No.e-inc- 7 deBrogle wavelength, 4= Ay_ my 1_1v CS: NovofeninCst 2 7 hg my 49% zee) “4 nd 3 9 ke=ta* 2 = KE; _m fl KE, m : KE; ~m,"¥ so, At ae "oh One ‘8 (©) Fe(II) =[Ar] 3d° unpaired electrons = 5; ea2e3.14x053A ——— 3328x107! m a 9, Ratio= V7: /3 0.3328x10-m=03328am ; 4 @ Co(II) = [Ar] 3d unpaired electrons = 3; 4) 53=2) fa 1) MLO? @F 2 © 10. @) m=1ém, eet oe [ence 5. @ ForBalmer n,22andny | ix x9m, HV Tea 11. (6) Fromihe given data, we have ver z Ee-Ep + E, 6 (©. Seriesimitisthe latin ofthe series, e.ny= 0. he he) _ he Ia te «joe GP_3371 DPP/ CCO2 $51 h 1c te 16 © az-nsrean (4-2) ‘Ax (given) a soiree SoM 62x10 au108 rs 6.5010" 3108 x4 2178x1018 x3 214 107m 13, @ (o+drletichighertivalveof (n+ D,thehighris 17. ©) Not more than two electrons can be presen in same the energy: When (a+ 1) value is the same see omic otal, Thisis Pal sexlson pencil value of n. 18. (a) 2 excited state will be the 3 energy level. ii 36 136 @)_ G)_ Go GD GD Eu=ae va bS1ev. a 18. 0) Calelaing number oflesrons Weta i 2 nol osvaaaem 14 @ 1e=Zetseev 0 1 cof) —y6+8x342 22h sotetoic ses nat Nog 97483341232 h we Zz ii) wee z,=2, sof’ 1683+ ny=1,Z,~Satdin=1 2 cof om ote pin Stbsiting thes values in equation i) * 196x108 4 1 NO3 —>82 ox 6es1=14 or hy 112-14 biwetsonic gsi ==4.41 x 10-7 atom Bh5 " : “pee 1. (©) AsperBohr's poste, j—y6n2+2814 1h 2 rok iseaeas3e30 4 $0} —916+8+2050 bisoceaonc pce ciog 1748x4412 59 Hence the species in option (b) are not isoelectronic 20, @ (AE), The energy required to excite an electron in an atom of hydrogen from n= I ton=2is AE (lfference in since, r= 20% energy E, and) So. for 2" Bob obit Values of and Ear, agx2 Fy TBO a sossmort Sie or aa 2H? AE is given by the relation, (az) ee Ax me x(4ay) [AE=E,—E, =(-3.28 105-1312 108 }Jmot e 3.28% 108 +1 312% 105)3 mot! Boxee 984% 108 Fmot! ‘Thus the correct answer is (d) DPP/ CC02 Sabtiutng tis in eqution 6) ny2-(4-4) Le 2 de my = 3,4, Sine Last line of mV2KE the secu ead sei 1 Limiting line is the tine of shortest wavelength and "KBD @) igh energy when men 1 Ry _3.29x10! _ 3.2910! je he eoF!!lUS VKE no when KE become ines wavelength bom 12 =322610s 21.) Thecletenecontguraon of Raum (3 22 Energy eed esk one mae of IC tandsin aetna ae Since las elon nein Sv ital Gensco Hence n=5.1=0,m=0, 224 6.626310" «3108 28. (@) The kinetic energy of the ejected electron is given by ar de onnton 48:26 10-3108 6.023.102 weivgetm? os ve£ 242x108 B Bs 0.4947 x 106m =494.7 nm 2.) a= hor 10%5 m0 4 ©) «o> ay Ym aa, a 29. @ Taal energy ofa rosin elecron isthe sam fis : Talon KEY PE aot a Gray 2 { 2) ao alr) (= 2repreent doit i which > 0. b) nergy of I mole of photons, 26. (b) de ~ Broglie wavelength is given by " B= No xh @ Noxhxe a 6.023107? x6,63%10- «3108 253.7109 m2 nergy coneredino KE=(4722-8053)13 ana-43059 ‘4 of energy converted int KE.» 4722-42089, =8.76% GP_3371 @ © © 4 ® 5 © 8 © DAILY PRACTICE PROBLEMS All the given species contains 10 e- each ice isoelectronic. For isoelectronic species anion having high negative ‘charge is largest in size and the cation having high positive charge is smallest ‘Covalent radius s radius of an atom in its bound state ice, in fluorine it is half of distance between two ‘covalently bonded fluorine atoms; van der Waal radii is one-half ofthe distance between the nuclei of two identical non-bonded isolated atoms, These atoms are attracted toward each other through weak van der ‘Waal’s force hence van der Waal radi are very large All the given species are isoelectronic. In case of isoelectronic species ionic rai increases with increase in negative charge on anions. ‘On moving along the period, ionization enthalpy Insecond period, the order ofionization enthalpy should be as follows F>0>N. ButNhashalffiled structure, therefore, itis more stable than O. That is why its ionization enthalpy is higher than O. Thus, the correct order of TE is FSN>0. In a period the value of ionisation potential increases from left to right with breaks where the atoms have some what stable configuration. In this case N has half filled stable orbitals. Hence has highest ionisation ‘energy. Thus the correct order is B oxides of sulfur > oxides of carbon, ‘Among oxides of earbon acidic character increases with the oxidation number ofearbon.So, “CO, ismoreacidic than CO. Hence the sequence of acidic characteris N,O, >S0,>CO,>CO ‘The ionization energy increases with decrease in size. Further the element having stable configuration has higher ionisation energy than expected. Hence the ‘nization energy of nitrogen (Z=7)ismore than oxygen (Z=8) and carbon (Z.= 6) because it has half-filled p-orbitals Sc = 1522s? 2p? sgN = s?2s?2p! 40 = 122522 p4 Hence the correct order should be CO 9. 10, ML. 2. B. 4 15, 16. CHEMISTRY SOLUTIONS » @ @ © ® @ » ® ® ® phd} Along the period, LP generallyincreases but notregulaly Be and B are exceptions. First LP. increases in moving from left toright in period, but LP. ofB is lower than Be. ‘The electronic configuration ofthe given ions are as follows. Mee Le, 222298 (Nounpuired electron) 2sTi**= 1s2,282pf, 33p?3d (One unpaired electron) pV" = 1, 222325 (Twounpaired electrons) gh ES 1, 2298 30233 (Four unpaired electrons) TE, of Mg is lower than that of Na because in case of, Mg", 3s-clectron has tobe removed whereas incase ‘of Na, an electron is removed from the stable inert ‘gas configuration which is dificult ‘According tomodern periodic law, the properties of the clementsare repeated aftr certain regular intervals when these elements are arranged in order of their increasing atomic numbers For isoelectronic species, sizeof anion increases as negative charge increases whereas size of cation decreases with increase in postive charge, Further ionic radii of anions is more than that of cations. Thus the corectorderis Ca"t PH, > AsH, > SbH, ‘The right sequence of LE, of LiF>Br>L b88_-—<—o@ ————_——— P/ CC03 19. (On moving along a period ionic radi decreases due to 20, a. 2. @ @ @ increase ineffective nuclear charge ‘As the nuclear charge increases, the force of attraction between the nucleus and the incoming electron increases and hence the elecron gain enthalpy becomes ‘more negative, hence the correct order is CaF further Li* and B® are isoelectronic. therefore Lit > BY Hence the correct order of atomic size is, O->F>Lit> BY ‘As the size inereases the basic nature of oxides changes to acidic nature ie., acidic nature increases. 80, >P,0;>Si0,> Al,0, ‘cite "Wek Anghottic SO, and PO, are acidic as their corresponding acids H,$0, and HPO, are strong acids. For isoelectronic species ionic radii decreases as the ‘charge on ion decreases. Further on moving down in a ‘group ionic radii increases. Hence the correct order is Oh ene sh

,Co, Silica (SiO,)is insoluble in water and acts asa very ‘weak acid ‘SnO, is amphoteric as itreacts with both acid and base, ‘SnO, + 2H,S0,—> Sn(S0,), + HO Sn0, + 2KOH———> K,$n0, + H,0 Incoming electrons occupies the smaller also negative charge on oxygen (O°) is another factor due to which incoming electron feel repulsion, Hence electron repulsion outweigh the stability gained by achieving noble gas configuration. In the isoelectronic species, all isoelectronic anions belong to the same period and cations to the next perio. T represents Li, I represents K represents Br, IV represents 1 V represents He So, amongst these, II represents most reactive metal ‘and V represents least reactive non-metal Helium (He) 1s? ~ Highest ionisation energy due to noble gas innature. Fluorine (F) 1s?,2s?2p? —> High electronegativity in nature dueto small size and -1 oxidation state. Rubidium Rb) > Most electronegative element due tolarge atomic size Lithium, > Strongest reducing agent due to small size and positive oxidation state (+1) GP_3371 5. DAILY PRACTICE PROBLEMS © @ © © x ce A COF Its structure is Greater the difference in electronegativity between the ‘wo atoms, larger will be polarity and hence dipole ‘moment. Thus (a) has maximum dipole moment, a HC UH fe ¥ : H.C H.C’ Sc Symmetrical molecules (= 0) [NH undergoes H-bonding and hence has the highest bp. Among the remaining hydrides i.e, PH ASH and SbH, as we move from PH, to BiH, the molecular ‘mass increases, Asa result the van der waal's forces of attraction increases and the boiling point increases regularly from PH, to BiH A Bich, CI=BiC(, sp? Hybridisation (Trigonl planar geometry), Bond angle= 120" gp we InPCl; (Pyramidal Tere geome | pond angie yp telow 103 Tasch, av Pyne | 22 Sereates fom GET mein) |PCHIPBIC Bic, SA” ceyramidat ENG somes) In these, order of bond angle BCI,>PCL,>AsC, > BiCl, In NH, the atomic dipole (orbital dipole due to lone pir) and bond dipole arein the same direction whereas in NF, these are in opposite direction so in the former case they are added up whereas in the later case net CHEMISTRY SOLUTIONS i) © @ Nyrottoris? oaora? { @ phd results reduction of dipole moment. Ithas been shown inthe following figure : : K 4» 4 i } Molecular orbital configuration of wl 293 ‘Te correct onderis = NP - (No. of valence electrons of central atom + No, of monovalent atoms attached toit + Negative charge if any ~ Positive charge if any] NO H=15+0+1-0) NOs H=3{5+041-0 Ha dseatie NHyy H=2(5+2+1+0) 1s10-——__________________——- DPP/ CC 04 16. @) 10. © 2 © B. © 4 @ 18. - Nis, H=315+4+0-1) SCN- =p ite, NO;- and NO; have same hybridisation lesronegaivity differences 40-120=28 percentage ionic characteris 72.24% when the electronegativty ditferenceis 1.7, the ionic characteris appro 51% In POY ion, formal charge on each O-atom of P-O Totaleharge __ 3 amber of O atom "47 ~°75 ‘The electronic configuration of the given molecules bond Nj Ip—bp> bp-bp In NH and BE; the hybridisation ssp? and the bond angleis almost 10928. In XeF, Total numberof valence electrons of Xe = 8, two electrons shared with 2F atoms, 6 electrons let hhence 3 lone pairs, in XeF, 4 shared with 4 F atoms 4 lefthence 2 lone pairs in XeF 6 shared with 6 Fatoms 2lefthence | lone par. ‘No.of electrons 1 Hybridisation = 3] in valence f+ shell of atom <7 Cz toms around it cation (ar “) For Hybridisation ofA atom = -3-99 oral. Hybridisation ofA atom = 434-041) =4asp? For H,0, Hybridisation of © atom 1 2 For H,0*, Hybridisation of atom [s+2-0+0] =4 =? = Ho+3-1+0] =4 =sp° ForNHy Hybridisation of N atom = 3lo+3-0+9] a4an% For NH, Hybridisation of N atom 3 ‘Thus hybridisation changes only in option (a). Hoe4-1+0] GP_3371 DPP/ CC04 20, a. 2. 23, 26. © © Hybridisation in PO} = 44 [5 + 0+ 3-0) =4 sp?.tn bonding only d orbital of Pp orbital of O can be involved. Since hybrid atomic orbitals do not form x bond. ‘The bond angle decreases on moving down the group due to decrease in bod pair-bond pair repulsion. NH, PH, ASH, SbH, Bil, or 98 or) oop ‘This can also be explained bythe fact that asthe size of central atom increases sp? hybrid orbital becomes ‘more distinct with increasing sizeof central atom i.e pre p orbitals are utilized in M-H bonding For any species to have same bond order we can expect them to have same numberof electrons. Calculating the numberof electrons in various species. 038+8+1=17); CN-(6+7+1=14) NO‘ +8-1= 14,CN'6+7-1= 12) We find CN- and NO* both have 4 electrons so they hhave same bond order. Correct answer is (3). © @ fo of of (xf = xB) OM(NS = 1Selectrons) it comin one unpaired electron hence paramagnetic The dlocalised pR—PR bonding between filed p- orbital of Fand vacant porta of leads to shortening Of B-F bond length which results in higher bond dissociation energy of the B-F bond © Vecant Filled aporttal —2porbital R KR Ns-r— 5 aan A RK F Nace Ss 3 ee yo (©) Compounds involved in chelation become non-polar, B-P— 2. 30. ® @ ® st Consequently such compounds are soluble in non polar solvents like ether, benzene etc. and are only Sparingly soluble in water whereas meta and para isomers are more soluble in water & less soluble in non-polr solvents So intra-molecular H-bonding ‘According to Fajan’s rules smaller, highly charged ‘ation has greatest covalent character with smaller charge has greatest ionic e None of the given option is correct. ‘The molecular orbital configuration of the given rmoleculesis H, = ols? (no electron anti-bonding) Lig= ols? o°Is202e%¢wo anti-bonding electrons) B,=als?o"ls? 02 "2s {x2p = x2p2} ant-bonding electrons) ‘Though the bond order ofall the species are same (B.O = I) but stability is different. This is due to difference inthe presence of no. of anti-bonding electron Higher the no. of anti-bonding electron lower is the stability hence the correct order is Hy > Lig > By ‘The structure of IF,” is distorted octahedral ‘Thisis due to presence of a “weak” lone pair. ‘The molecular orbital configuration ofthe molecules givenis Total no of electrons in NO = 1(N) +8(0) = 15, Hence E.C. of NO= KKIo(2s)P'[o*(2s)'lo2p,1° 2p PPP PROP. Due to presence of one unpaired electron NO is paramagnetic. Except NO all are diamagnetic due to absence of unpaired electrons. CHEMISTRY DAILY PRACTICE PROBLEMS SOLUTIONS DPP/CCO5 ae 1 Meo¥d scone proses fo oe 8.6) Ratcofditson« [1 24M mote Molecular massofHCl > Maer mass oN, 273 373 HCI diffuses at slower rate and white ammoniur 2 (@) From the graph we can see the correct order of pressures chloride is first formed near HC] bottle. nope 3) Gonclbantedunghktomssepnsonaly - — Uco, | Foo,Whso if they are below a certain temperature known as inversion % (@) temperature 7) Theinversontemperaturescharacerisicof no Meo, “70 cach gus ands given by fFco, 44 = Ty,0 =16Tco, 7,= 22, where Ris gas constant o Given ¢=0.244 am L? mot? © = 7 027 Lol! R=0.0821 L atm deg-! mot! __2x0244 ~ D027 0.082 2 4 @ uaF orm /uy= JiR m3 yaa (300 “Vox7+273 ~ V1200 2 =2y = 5. @ Letthemass ofmethane and oxygen =m gm. Mole fraction of 0, 1. @ Moles of O> ‘Moles of 0, + Motes of CHy mw ~ ia/a2+mii6 ~ 3m/32 ~ 3 Partial pressure of = Total pressure x moe fraction of 20K Tr (ay nig) My (mp +p) Mp eververy ‘Mean molar mass = Mp 2 © 6 © Ums(O2) | 3R(GO0K)/G2g mot 7. (a) Given T=20°C=27 +273=300K gas (Ha) [mae 21.6-20.1 2-3 Mass of nitrogen = 14 g nHe=0.4/4=0.1 13, @ KEof neon at 40°C KE of neon at 20°C 313 283 10 GP_3371 DPP/ CCO$ td 14, (©) Higher the critical temperature more easily wil be the ‘2asliquify. Now since most easily liquifiable gas show larger deviation, NH will show maximum deviation from ideal behaviour. ‘According to Avogadro's law "At same temperature ‘and pressure Volume «no. of moles” Hy = 53 Ro, 35h Vins Noy: Very =" 18. © “232 Given, M1, =, ad ty, = toy According to Graham's law of diffusion for two different ‘gases. 2 16. «@ [Moz \Mu, wit fo, Yalta Vie=4 Fraction of 0, = V8 17. (©) As temperature rises the most probable speed increases and the fraction of molecules possessing most probable speed decreases. According tokinetc theory the gas molecules are in a state of constant rapid motion in all possible directions colloiding in a random manner with one another and with the walls of the container and between two successive collisions molecules travel in a straight line path but show haphazard motion due to collisions. According to Boyle's law, PV = constant log P + log V = constant log P = - log V + constant Hence, the plot of log P vs log Vis straight line with negative in tog P| WN log V—> CO, +C—2C0 Stoichoimetry ratio is 1: 2 AT STP, P= 1 atm, T= 273 K, 8 @) v. © 0821 Pv Initial moles of CO,, m(COsinitial) = Fr 1x05 010821273 In final mixture no, of moles; n(CO.JCO mixture) = 0.022 mole 1x07 ~ 90821273 Increase in volume is by = 0.031 ~ 0.022 = 0.009 mole of gas Final no, of moles of CO i.e. mco faa) 0.031 0 finat) = 2%(COp inital) ~ "(COp fin) = 20.022 — Meo, fay © 0 tay = 9.044 = 2mo, ay ~AHD Now, "co fnat) * "(CO finaly = 0-031 "cog ea) = 2.31 ~ M0 gy) Substituting (i) in ea.) C0 tay = 0.04 ~ 210.081 ~ Mo pany 1.044 ~ 0.062 + 2n¢c0 fay 018 mo. "0 taal CO Ha) = Volume of Co =v =2RT._ 00180.0821%273 P 1 = 040 Live and volume of CO, = 0.7 litre ~ 0.4 Titre = 03 litre CO, = 300 mL, CO = 400 mL PRT 21. (©) Most probable speed (C*) RT oR ar Pe According to Graham's Law Diffusion: Volof gasditfused V) ime taken for difusion() Milt Since rate of diffusion ny Vally My 20/60 _ [ie/> 3272 = = ¥,730 .: Mol. wt=2x VD Oncalculating, Vy= 141 Is14 23. @_ ems. velocity Vem 4, 28. . @) © (a) 7 y, nai) = Vem [RTs _ [BRT Vito, To. Mo, Mie 30032 t 2400k OG Compressiity factor (2) (For one mole ofreal gas) vvan det Waals equation At low pressure, volume is very large and hence correction term b ean be neglected in comparison to very large volume of V. ie V-baV Hence, ver ‘According to Boyle's law MA, 150,360 WR, 80 1750mI= 1.750 m1. 28, 29, DPP/ CCO5 (@ Onapplying Dalton’s law, Partial pressure of a component fle fraction « Total pressure Given, mass of N, = 56g, mass of 0, = 96 g Total pressure = 10atm $69 19, Ny PN, =O 10=4 atm, "0, =0.6% I x12 _ 96. (©) Moles of A (1) RT RT Ppp _8x5_ 40 Moles of (ng) = OP = ap ‘Total pressure x total volume = (+ hy) x RT 36.40 -0o(er/ "er 48am Panial pressure of B=68-48=2am, (@ Number of motes of Oy = 2-8 = 2.21 mol 32gmol Number ofmoles of Ne = 167-58 — 8.375 mot 2ogmor 2a Mole fraction of , = 55724 ===021 Mole fraction of Ne= 1-021 =0.79 Paral pressure of gas = Mole fraction x total pressure Pata pressure of 0, ~021 x25 5.25 bar Partial pressure of Ne=0.79 x 25 = 19.75 bar 30.0) Vo= qr = VROTTD Ug = EZR = {5 BTR = VB) GP_3371 2 3. 6 DAILY PRACTICE @ PROBLEMS 1000 (1 «8.314 373) 37898.88 mol" ~ 37.9 kimol Internal energy is dependent upon temperature and according to first law of thermodynamics total energy of an isolated system remains same, ie, ina system of constant mass, energy can neither be created nor destroyed by any physical or chemical change but can be transformed from one form to another AE=q+W For closed insulated container, q= 0, s0, AE = + W, as work is done by the system (©) Maximum work done by a system at constant pressure (@) as: © © ‘and constant temperature is -AG. It can be derived as follows: From first law of thermodynamics, G= AE # Mey, Mon ex. ‘At constant pressure, Wor = PAV Q=AE + PAV + Wopmexp. = AH + Wo ep. For the reversible change atc a st temp, Grew 7 AS= 98% 0 Gey =TAS SY Gey so from equ. (1), TAS = AH+ Wa exp => AH ~TAS = -Waon exp. 2) Fora change taking place under constant pressure and constant temperature, AH-TAS= AG so from equ (2) AG =~ exp Gt means Waonerp. OF Was) Of Wy = AG Latent heat of fusion ‘Melting point a T 2930 300 Desired equation is H0(1) >H,0(g), AH. (Equation 1 - Equation 1) AH=-2455 KI -(-286K))=40.5 1) Np +3H;—>2NH,, AH =2x~460 ki mol! Let x be the bond enthalpy of N—H bond then [Note :Enthalpy of formation or bond formation enthalpy is given which isnegative but the given reaction involves bond breaking hence values should be taken as positive.) AH = Bond energies of reactants ~ 2 Bond energies of products IK" mol 9.7711 mol! CHEMISTRY SOLUTIONS zo & © a (a) 10. phd) 2x=46=712+3 x(436)~6r =92=2020-6x 6x=2020-+92 6x=2112 224 352KNmol Alls. 5+2MHy.=239 2AMy.s =175 Hence, AHs_g =239-175 = 64 keal mot" ‘Then, AH for 85,g) > Sui) is 8 (-64) =-S12keal Enthalpy of reaction = BE Reason) BE pracy) = [BE cca + 4BEcc-1) + BE aw | -[BEc-0 + 6BE cw] [606.1 + (44105) 431.37)] [336.49 + (6x-410.5)] 1200k)mol"! Given, for reaction (OHO —>H" aq) + OH" (aq. AH, =57.3210 wry L0)— 000 AH, = -286.20 kd For reaction () AH, = AH®,(H* ag)+4H°, (OH” aq) AH’, (0,0) 57.32 = 0+ AH’, (OH” ag) ~ AH", (H,0,0) « For reaction (i) Al, = AH; (1,0, 0 ~ 1 AH? (Ha, @)~ AH" (2.8) 286.20 = AH (H20, 0) ‘On replacing this value in eq, (i) we have 57.32 = AH" (OH™ ag) ~ (-286.20) ‘AH®, (OH™, aq) = -286.20-+ 57.32 = -228.88 KI Atequilibrium AG=0 For a spontaneous reaction ‘AG must benegative wich isposibleonlyif AH TAS <0 ‘AH ner Ds 1s46-——__________________—— DPP/ CC06 n. 2 1B. 4 1s. 16. © @ © © @ 2C gH) 250249) —P16CO 34) +18H20 ‘The given reaction is @ combustion reaction. Hence this will bean exothermic reaction. ie AH=—ve FurtherAn=+ve ie. AS AG= AH-TAS=-AH-TAS. AG = AH-TAS, AH + ve, AS is+ ve: TAS > AH for spontaneous process. twill make AG. ~ve ‘We have to calculate the enthalpy of the reaction OH) +0) + Hig) From the given rections, this can be obtained as follows. team + F@) 2) aH £ 435:891I mort + <495.05%s mot 1 + 5 (0x) 200@); A= 5 Add ORG) H@+O@ 3 AH= 423.3815 mol CH, +20, —+C0, +2H,0 x) CyHy + 50, —>300;+4H,0 Gy 38) De 5S = s=3L ~ Heat released 3 6 890+ 22220 =317 na Da C+0;-¥€0, + 393.5 K/mol Rg tg 44gis formed from 12g of carbon 1235.2 a 35.2giis formed from of C =9.6g ofC=9.6/12=0.8mole 1 mole release heat 393.515 ,8mole release heat = 393.5 0.8 =314 81) 315K) @ 2C{s)+Hy(@) —+ H-C =C-Hig) ‘AH=225 ki mol Gi) 2) —+2C@) AH= 1410) mot coy seat 2 rosa! Gi) Hyg) —> 2H) AH=330kI mol! enenin 2s [Pely gy BB] ~[2xBEc_y +1*BEc.c] 225 (1410+ 1 x330]-[2x350+1xBEcec] 1. @ B® vw © 2» © a. © 2 @ AG=AH-TAS For a reaction tobe spontaneous, AG = -¥e ie,AHa25k AG=AH-Tas ‘Since AG = AH~TAS for an endothermic reaction, ‘AH= +ve and at low temperature AS =+ ve Hence AG=(+) AH—T (+ )AS andifTAS AH. ‘The standard enthalpy of the combustion of glucose «ean be calculated by the eg. CH ,,048)+ 604f8) > 6CO,(2) + 6H00 AH = 6 AH{CO,) + 6 AH; (H,0)—AH,[CH20g] AH? =6(-400) + (-300)—(-1300) AHP =-2900k/mol For one gram of glucose, enthalpy of combustion ane =- 2%. 180 (CH, = CH, (g) + Hy(@ —> CH -CH, Enthalpy change = Bond energy of reactants ~ Bond energy of products. AH=1(C=0+4(C-H)+1(H-H)-1C-0)-6(C-H) =1(C=C)+1(H-H)-1(C-0)-2(C-) =6154+435—347-2x<414 = 1050-1175 =-125 1, For a reaction to be at equilibrium AG = 0. Since AG = AH—TAS so at equilibrium AH-TAS=0 or AH=Tas For the reaction 16.1113 gm $x. 4g% x: AH =-304) (given) Calculating AS forthe above rection, we get as=50-[b.60+3:40)px" aaae) =50.-(30-+60)4K"1 = 40K"! Atequilibrium, TAS = AH 1365) +Cly(g)—>21CK) GP_3371 DPP/ CCO6 —_$ A i AH = [AH(L(s) 91,(8)) + AH, 1+ Hey cy) (AH, ci) 26.) —Wireyersbie = Peat (Vo ~ V1) = 151.0+242.3+ 6276-22113 =3346 }Oatm 2L— IL) Daim —L tracy = 324 1673 : Pav 23. @) 3H) + 7X2 —> HX A Let the bond enthalpy of X —X_ bond be x. =2.303 nRT log VE h 1 1 50= 54H yy 5AHx-x ~ AH x. 2 = 12.3030.0821 atm-L/K /mol x log > = tone bee = 16.96 atm-L 2 2 Woven 1696 1 gy a7 2=100 KI mol” Woreversiie 10.00 27.) For moles of gasat temperature T, 24. @) Nx@)+5.03->N,0@) Pv =Ser NeNG@ +4{0-0)- 8-8-6 For mols of gas at temperature T-2, 2 PV, =SR(T~2) Energy required for breaking of bonds) {Energy released for forming of bonds} An! 1 = Hyon + 5AHo.0 ~ (OHy.n + AHy.0) renin aerate ise 28 (@) CzH,OH(0)+303(g)—+ 2C0y(g) +3430 = (046+4498)—(418+607) =1701 mol" 2 Bomb calorimeter gives AU of the reaction Resonance energy = 170-82 = 88kJ mol” Given, AU=-1368.4715 mol" net lac! 2. Anyvton—suer essn4nc9e 2 2 AH= AU+ An,RT: 136447-—To9 Afige) “BE. of estan 136699" 29. tb) 2, 0) AS°=S%¢o, +2*S%u,9~[Seu, #2%80,) (213.6 + 2 x 69.9) — (186.2 +2 205.2) 242. 8K! mol"! = SBE of products Leasoe tet = 4304441 240-BE.of HCI 90 t304 5 S20 BE of HC BE of HCI=215 + 120+ 90 =425 kd mol! DAILY PRACTICE PROBLEMS L. 0) K,=K,(RT)™sinceAn=0, 2 G@) Kyat 25°C=1 x 10-4 Asc K-18 ][01"]= 10" At 100°C(givem K,,=[H"] [OH]=55 x 10-* 2 fora weal ottion (H"]=[0H] (HP =55 x 10-4 ce} =65% 10! + pH=—log(H") (On taking log on both side ~log [H"]=-Iog (55% 10-4)! 6 ® Now from Handerson equation [salt] HH = pK, + log SA 1 ©) PL = DK Dog a ») Putting the values, {Sak [Acid] 5= 44 log. [sai ves aa = 5 Taking antlog [SaltfAcid]= 10= 10:1 4. (@) The reaction given is an exothermic reaction thus according to Le chatalier’s principle lowering of temperature, addition of F, and Cl favour the forward direction and hence the production of CIF, 5. © AgyC10, Kyp=(Ag"P [C07] = 1.1 10-1 4=1 a @ %. Asch Kyy=[Ag*](CH}=1.8% 107 18x10" lag'l= (or) CHEMISTRY SOLUTIONS idee AgBr Kp=[ag') Br} =5.0.10- 25310" ag’) =53x10 ee Bl al Ky=[Ag']tr]=83% 10-7 tag?) 8310" m1 tre take [0402 ]=[Cr (Be 1=1F1=1 than maximum [Ag?] will be required in ase of Ag;C1Oy MY SM'+Y" Kgp=9?=62% 108 vo2x1 82787107 mol Lt NY, SN 43> Kgp=x (G9? =206¢ (sosezy" or $=389% 10-4 mol molar solubility of NY, is more than MY in water. AG y= 86.6k Jmol = 86600 Jmol GNoy) = xml T=298,K, = 1.6% 10" ae Given equation, 2NOG)+0,(@) —=* 2NO) 2G, ~246" =~ R298) ln (1.6 10%) 2G", 2 86600 =—R 298) n (1.6 10°) 2G yy, = 2 86600-R 298) In (1.610) 2x10! -RTInK, AG og= (286600 R298) (1.651 =05 (2 86600 -R 298) In (1.6% 10°) ‘Clausius ~Clapeyron's equation ane a GP_3371 DPP/ CCO7 ——— 8s aome4o,—0% Apbingt 3 I-D weit “we anit $0p-E2N0 124404 (NoP_, [0 Nay? NaJ[O2] [ry «{0,)°?/ [Na][HaP K=K,x K3/K, 410, (Initially on increasing temperature rate of reaction will Increase, 0% yield will als increase with time. But at equilibrium 9% yield at high temperature (T,) would be less than at Tas reaction is exothermic so the graph is 15.) ML, (©) Ag:C:04(9}—=2As" (a) + C20F (a) Ksp= As"? (C,071 TAg']=2.2% 104M, = 110M Kgp=(22x 1042 (1.1104) 16.@ =5.324x 10-1? 12) Fora gaseous phase eatin K, and K, are elated as Ky = KRY Forthe given reaction, COW) + $021) CO, 1 Ang= 1-(1+05)=-05 00-5 1 - 2 Kyo KART) 1.@ Ky 2 or =P = (ary? K 13.0) PCls == PCs + Cl, Ima aoa oP a? a K, onKy=@2P a= ISP when 1a’ P Max. pressure of CO, = Pressureof CO, at equilibrium Forreaction, SCO{S) —= S109) +CO, K,=Poo2= 16atm=maximum pressure of CO, volume of container at this stage. RT 0 ‘Since containers sealed and reaction was not earlier at exilim, ‘n= constant. PV _ 04x20 RT RT 2 Patequation (i) in equation) 2 ax 20} RT vl" er tis ©69)+ CO) 20048) Apply law of mass action, Poo) og 63.~ Peo, 0, Poo. Given Kp=63) and Peo = 10%, 2 Ky Prasat =Poo, + Poo =0.63+ 63=6.93 atm, HA: HAT 5 = CC UIHAT) kK, = 10 x 108 = IAT Given) (Al HAH +A Ky =5.0x10-1 = ETA A Given) (HAT) WPA] THA = (1.0% 105) (6 « 10°) =5 10 Letthe weak monoacidic base be BOH, then the reaction that occurs during titration is BOH HCI BC! +H,0 Exilim: B+ H,0—BOH+H* Kix ky ae a Using the normaly equation, N= Nas co tae) Substituting various piven values, we get 2ey cas? is 3 18. ©) 5x3=75 ml ‘Then the concentration of BCI in resulting solution is sven by 521 wom 10 10“ (Toa volume=2.5+7.5=10ml} since ky = Ke. an * or 107-107 h=0.1 h* or 0.1h2+107h- 10° (Solving this quadratic equation for h, we get) -ps Vie | wn =1077 + 00)? +4107 x10" 2x01 or? Yor + 410-3 201 01+ 0001 + 0.004 02 0.01 J00081 “on 0.010.064 02 Thus the correct answer is [dl MiVi=MaV2 1<0.10=M3 x 100 M)=0.001 = 10 BOH ——=B" + 0nr c 0G ca Ca Cu _CaxCa, Cd=a) Ky=Ca? a= \KIC - Ke for =ca=/ (:l-axd Re © 21. @) 2.) Ba) 25. @ 26. @ Lets =solutility AgIO}—=Ag* + 10° K,=[Ag' 0, }]=sx0=2 Given Ky= 110 IK, = Vix1o® 1.0% 10 moti = 1.0% 104 283 git (/+ Molecular mass of Ag 10; = 283) _ 10x10 2833100 ~~ i000 = 2.83% 10° gm 100ml (180,) can accept and donate a proton (HS0{) + HY > 1,80, (acting as base) (S04) Hr + SO, (acting asacid) 0/1001 Mg(OH), -> (Mg”*] + 2{0H7] x k= [Ma] [OW = [s]2xP=x.42 HOH) () —= Cr" (ag) +308") sr ©) GP=K, 21S! = Ky ey (veni02)" 2 2 [Cu(tl,0),P* +4NH, = [CuNH,),P* + 41,0 invohes ose and gan ofeletrons. H,O is coordinated toCu by donating electrons (LHS) Itis then removed by withdrawing electrons. pHof an acidic solution should belessthan 7. The reason isthatfrom,O. [H"] =107™M which cannotbe neglected in comparison to 10M. The pH can be calculated as. from acid, (H'] = 109M. from H,0,[H]= 107M » Total (H"]= 10% 107 109(1 + 10)= 11104 ~log(H*] =-Hog 110% flog + 81g 10) “olumest water ded = 10-19 Forte reasions 2NOz(e) NO(e) +09 (8) GP_3371 DPP/ CCo7 ——— st Given K,=1.8%10% at 184°C R=00831 kjmol.k £8 10-° 0.0831 «457 = 6.836% 10° [5 184°C= 273 + 184) =457k, An=@+1,-D=1] Hence itis clear that K,> K, 27.6) [25(POx),} 374 APO 2783 «25654 = 691287, (" 28, (©) In aqueous solution BA (salt) hyrolyses to give BA +H,0 —= BOH+HA Base aci Now pHs given by Lee lig H=1pk, +4 pKa—-1pk, PH=3pKy +3pKa->pKy, substituting given values, we get pte basy480-470 =70 29. 0) Ce{S0)s= 208°" +380, ae K, = 2s)? G9 4st 27° = 1088 Cal Hg,Cl, > 2Hy* + 21° . panies crcl, 5 ce 3c ae Ky=s% Gs) =2794 -(SJ" Hence the correct order of solubilities of salts is emo at)“ >(Se) "(Re)" NaCN is a salt of strong base and weak acid; pH Liged =7+4pk,+Llogc 2PKa ty DK for HC \4-470=9,30 1 1 pH =7+4%9,30+1og0.5;pH =11.5 pH =74+5 3lo80.50 DAILY PRACTICE PROBLEMS (@ ON.of Nin NO, andN,0,is+4 diference ize ON.ofPinPOgandPOyis+5 erences zor ONdANinN Oi ndinNOiss2-Tedierncis! ON et SinOyiandinSOyis¥6 The dilenceis 2. @ 2 s2aien = ab +280), wae ‘The oxidation sate showsachange onlin) (b) Magnesium provides cathodic proton and prevent ranting or exrsin, @) 2K MnO +3804 -> K2S0, +2MNSO, +3830 +50 “2 ‘2 2FeS0,-+H3S04+0—> Fea($04)3 +H20 ON. of Mn changes from +7 t0+2 Reduction) ON. of changes fom #20 +3 (Oxidation) aereSe 9 8 (©) 2H1' +H,80,—o19 +80)+2H;0. In this reaction oxidation numberof Sis decreasing from + 6 0 ‘+4 hence undergoing reduction and for HI oxidation [Number of Tis increasing from =I to hence underegoing oxidation therefore H,SO, isacting as oxidising agent. (@) ()Mn®* + ne~ —» M, forthis reaction, high negative value ofE* indicates lower reduction potential, that means M will bea good reducing agent. ‘Stronger reducing agent => Easy to oxidise y Lower reduction potential = higher oxidation potential @ Bement Focl Brod Reduction potential +287 +136 +106 +054 Evol) As reduction potential decreases from fluorine toiodine, oxidising nature also decreases from fluorine to iodine. i) The size of halide ions increases from F~ to. The bigger ion can loose electron easily. Hence the reducing nature increases from HF to Hl (@) X MnO, + C0, +ZH° => First half reaction ‘MnO —>Man"* @ On balancing ‘MnOj 48H" + 5e” —>Mn"* + 4H,0 wo Second half reaction CHEMISTRY SOLUTIONS a @ 2 © 10.0) IL @ 12. @) B® 4. @ eyed) c,07 —+200, ai On balancing €,07 —>200, + 26° ww (On multiplying eqn. (ii) by 5 and (iv) by 2 and then adding we get 2Mn0; +5C,0;- +16H* —> 2Mn"* +10CO, +8H,0 Order of decreasing electrode potentials of Mg, K, Ba and Cais an 2.925 Epa? pa = 290 Ee 2.87 Highly negative value of £2, shows the least value of clectrode potential ‘On balancing the given reaction, we ind 3Na,HAsO, + NaBrO, + 6HCI SS ONC + 3H,A80,+ Nabe 2x=10; hhence the correct onder is $,0,-<80;~<8,0, G0, C1, LetO. No.of r= 2+2(-2)42C1=0 x-4-2=0 x=+6 If-an electronegative element is in its lowest possible ‘oxidation state in a compound or in free state. It can function as a powerful reducing agent. eg. Xe=53.5% -. F=46.5% Relative number of atoms Xe Simpleratio Xe= ONofXeis 16 Copper when exposed to moist air having CO,, It gets GP_3371 DPP/ CC08 —_—_$ A hd 15.) 16.) 17.@ 18. @) v@ 20.) 21.) 22.) superficially coated with a green layer of basic carbonate CuCO,.Cu (OH), Iniodomety, K,Cr,0, liberates I fom iodides (Nal or 1). Which titrated with Na,S,0, soluion, K,C,0, +1 +H’ —90P" +1, ere, one mole of K,Cr,0, acceps 6 mole of elesteons. ‘molecular weight uivalent weigh Eq al 5 “ H$0s (aq) + Sn** a) + H20(I) > Sn (ag)+ 1180," (aq)+3H" Hence HSO; is the reducing agent because it undergoes oxidation, aw C8 +2NsOH > NaCl+ NaClO+H,0 46 74s 3MnOj” +2H,0— 2NIn0} + MnO, + 40H “4 4s a 2NO2 +H,0-> HNO; +HNO2 Allundergo disproportonation ‘The reaction given is 1,02 + Fe +C,0,2°-—> Ce + Fe +00, €1,0,2> —> 2c On balancing MMH + Cr,0,2* + 6°—> 2C5* 4 7H,O 8) Fett — Feo pe ai €,02- —> 20, +26 ii) On adding al the thre equations. rj0,2-+ Fe" + COP + LAH + 3° > 2Cr+ + Fe +200, +7H,0 Hence he total no. of electrons involved inthe reaction H,S, the oxidation state of $ is ~ 2. So it cannot accept more electrons because on accepting 2 electrons S acequires a noble gas configuration. So it ean acts only as a reducing agent by loosing electron, On the other hhand, the oxidation state of S in SO, is +4 which is an intermediate oxidation state of sulphur soit can reduce as well oxidise. Tall the given compounds oxidation number of non metal is +4, AsC belongs togroup IV and tis in its maximum oxidation state. So, reduction in oxidation number of ‘nonmetal is not possible only in CO, As we know that reduction is always accompained by an increase in oxidation number ofreducing agent. So, CO, cannot acts as reducing agent among the given choices. “The balanced equation is 2CyHg +702 -> 4CO, + 61,0. Ratio ofthe coefficients of CO, and H,Ois4 : 6 or2:3. ‘The compound undergo oxidation itself and reduces others is known as reducing agent. In this reaction O. N. (fi changes from 010 +2 and hence Niactsasa reducing agent B@ 4. 25. @) 26.) 27. @) 28. @) 29.0 “1 wo 2HL +H,S0, > 1,+S0, +2H,0 Oridsed Reged Ran Reg ‘A reaction, in which a substance undergoes simultaneous ‘oxidation and reduction, is called disproportionation reaction, In these reactions, the same substance simultaneously acts as an oxidising agent and as a reducing agent. Here Cl undergoes simultaneous ‘oxidation and reduction, 2KOH + Cl; -> KCl+ KOCI+ H0, “eoa ° (O, has the structure ‘ON. oftwo $* atoms are +5 each and that of other two S ‘atoms is zero each, CrO,C1,, MnO,-; O.N. of Cr and Mn are +6 and +7 respectively 2 as 28203 (aq)+13(s) +8403 (aq)+21" (aa) 2 ° $,0} (aq) +2Br, (1)+5H,0()) > 280} (aq) +4Br” (aq) +10H"* (aq) Hence, bromine isa stronger oxidising agent than Ip, 3s, it oxiises$ of $302 10 SO}- whereas ty oxides i only into $403 ion, Higher the value of reduction potential higher will be the ‘oxidising power whereas the lower the value of reduction potential higher will be the reducing power. 45 46 +6 KCIO; +H,C,0, +80, >K380, “1 +KC1+ CO, +10 i.e. maximum change in oxidation number is observed in Clas w-). Zine gives H, gas with dil H,SO /HClbut not wth HNO, because in HNO,,NO,-ion isreduced and give NHNO,, NO, NO and NO, (based upon the concentration of HNO) [Zn+ 2HNO3 —+Zn(NO5)2 +2H}x4 (eaty %) HNO, +8H—>NH +311,0 Nils + HNO; —> NH,NO3 4Zn+10HNO3 —4Zn(NO5),+NHgNO3+3H;0 ‘Znis on the top position of hydrogen in electrochemical series, So Zn displaces H from dilute H,SO, and HCI with liberation of Zn+H,SO, > ZnSO, +H, ae Y aw 10. 2 DAILY PRACTICE PROBLEMS (©) He willnot displace hydrogen since itis present below hydrogen in ECS, ‘The correct option is (c). In H,O, hydrogen has + 1 ‘oxidation no. In Cal, hydrogen has —1 oxidation no, Occlusion is the phenomenon of adsorption of hydrogen by metal Itis due tohydrogen bonding when H,0 forms acage like structure in solid ice and density is reduced. Heavy water is stable. A fusion reaction is difficult to oceur because positively charged nuclei repel each other. At very high temperature ofthe order of 10 to 107K, the nuclei may have sufficient energy to overcome te repulsive forces and fuse. Itis for tis reason, fasion reactions are also called thermonuclear reactions. Hence, hydrogen can be fused to form helium at high temperature and high pressure, HE (aq) HX —+OH(aq)+ Hy(g) wwe aid] ar In this reaction H" acts as bronsted base as it accepts ‘one proton (H*) from H,0 and form Hy. HO. The key reactions are POO+ Hy$ > PbS+H,0 ick) PhS + SHO) PbSO,+4H30 (wie) When blackened statues are treated with HO, the PhS is oxidised to PbSO,, which is colourless (White. ‘The water gas is a combination of carbon and hydrogen. Itis used in manufacturing of methanol. cobalt 6 CO(g)+ 2H (2) SA CHLOH) Elements of group 7, 8 and 9 of d-block do not form hydrides at all, The inability of metals of group 7,8 and 9 of periodic table to form hytrides is refered to as hydrides gap of d-block. In these compounds H atoms are supposed to occupy interstitial position inthe metal lattices. They are also called non-stoichiometrie hyarides (Cu+4HNO,(conc,) —> Cu(NO,), +2NO, +2H,0 © © @ @ @ © © @ () (CgH OH + Na—CgHsO°Na* +1/2H 7 Mg + 2H,0(steam) —» Mg(OH), + Hy 7 HOH +Na—> CgHgO"Na* +1/2H2 NaH + 0 —+ NaOH + Hp 7 Hydrogen is not used in the synthesis of hydroquinone and tartaric acid. © CHEMISTRY SOLUTIONS 13. Ma 1s. 16. Ww. 18, yw. 20. a. DPP/CCO9 (Normality of 10V of 1,0, 8x 224 © In the structure of ice each molecule of H,0 is, surrounded by theee H,O moleculesin hexagonal honey ‘comb manner which results an open cage ike tustre Asaresult there area numberof hole’ er open spaces. In such a structure lesser number of molecules are packed per ml. When ice melts large no. of hydrogen bonds ate broken. The molecules therefore move into the holes or open spaces and come closer tocach other than they were in solid state. This result sharp increase in the density. Therefore ice has lower density than wate. 7xN ©) 24505 (aq)—8™45_, HO,SO0SO, Hag) —Hutobsis_, 14505 (aq) + 2H(aq) + H,0,(aq) (©) A diamagnetic substance contains no unpaired electon, H, is diamagnetic asit contains al paired electrons Hy =o}. HS=o}, Hi =o}, (iamapneti) (parenapctc) primo ot He = of, 01! (osrmgoec) (oar) () 224LofHt, aSTP=1 moleof H; 1 02241 off atSTP = 10.224 =0.01 moles. (@) Only lements having reduction potential less than - O.41V liberate hydrogen with cold water (@Inone electron species, such as H-atom, the energy of ‘rita depends oly on the principal quantum number, Hence answer (@) @ Chlorine has lone pair which it can donate to form coordinate bond while hydrogen cannot. (@)-MgCO, is insoluble in wate. (@) True peroxide contains 0-0 linkage and 03> ion. They give hydrogen peroxide with dil HO, a0; +H,80, (til) > BaS0, +H30 (@ Very pure hydrogen can be prepared by the action of ‘water on sodium hydride. GP_3371 DPP/ C¢o9g AA aA cs 4 © 25. (a) [NaH+ H,0 —> NaOH + H, 26. (@ Polyphosphates (eg. sodium hexa metaphosphate) (very pure Hyrogen) form soluble complexes with cations such as Cx, A Mg? and so they ae used as water softening agents. 2820) —*+2H,0+02 . rape 2KI+H0) > 2KOH+1, NanlNay(PO3)] + 20g" —o Nal Cag POs)-4N™ 2KMn0, +3480, +5H302 —> Sones boa Ks50,+2MnS0,4-+8H;0+80, 27 © Ono and para forms of hydrogen resemble in their ‘chemical properties. 1,0, acts as a reducing agent only in presence of strong oxidising agents (i.e, MnO,-)in acidic as well 78 (©) 02 has oxidizing and reducing properties both. asalkaline medium, 29. () Nag zeolite + CaCl > Ca zeolite + 2NaCl 2KMnO, + 3H;$0, +SH0—> 30. (© CHYQ+ LOW —Zco+ 3H, K2S04 + 2MnSOq + SH20 + 502 Mixture of CO and Hy is called water gas. DAILY PRACTICE PROBLEMS 1. @)_ Alkali metalsare highly electropositive and thus highly reducing Therefore reduction , double decomposition and displacement methods for their extraction are not suitable Only electrolytic methods are useful for their extraction 2 (A reducing agent is a substance which can loose electron and hence a reducing agent should have low ionisation energy. Now since ionisation energy decreases from Li to Cs, the reducing property should increase from Li to Cs. The only exception to this is. lithium, This is because the net process of converting an atom to an ion takes place in 3 steps. @ Mg) > Mig) Sublimation energy Gi) Mg) > Mi(g) +e~ _AH=Tonisation energy (Gil) M*(g)+H,0 > M* (aq) AH = Hydration energy ‘The large amount of energy liberated in hydration of Li (because ofits small size) makes the overall AH negative. ‘This accounts for the higher oxidation potential of lithium ce, its high reducing power. 3. (@)_ According toFajan rules, ionic character increases with increase in size ofthe cation and decrease in size ofthe anion, Thus, CsF has higher ionic character than NaC] and hence bond in CsF is stronger than in NaCl 4.) BaCO, formsa yellow ppt of barium chromate. BaCO, forms. white precipitate of BaSO,, BaCl, is soluble in wate, S. (a) The weaker the base, the less stable i its carbonate Since LiOH is the weakest base, hence Li,CO, has the lowest thermal stability. 6) Asoutermost electronic configuration of alkali metals is ns! and also their size are largest in their respective periods so their Ist LE will be lowest among the given options. As second electron is to be removed from complete shell ornoble gas core, sothe Ind LE. must be highest among te given options So qin comet 7. (a) As we move down the group, the lattice energies of ‘carbonates remain approximately the same. However the hydration energies of the metal cation decreases from Be™ to Ba, hence the solubilities of carbonates of the alkaline earth metal decrease down the group ‘mainly due to decreasing hydration energies of the cations from Be™* to Ba & (a) 4KO, +200, ->2K,CO, +30, KO, isused as an oxidising agent. Itis used as air purifier in space capsules, Submarines and breathing masks as it produces oxygen and remove carbon dioxide. 9 @)_ Halides of group [and Il impart characteristic colour to the flame due to low IE of the central atom. However, ionization energy of Be and Mg atoms is high due to their small size, hence they can't be excited to higher levels by Bunsen burner flame. Thus, their halides don't ‘impart colour to flame CHEMISTRY SOLUTIONS Phd shed) 10. (©) According to Fajan'srule, ‘Size ofeation ce Tonic character. Recall that size of metal (ion) increases while going ‘down the group, and decreases on crossing the periods from left to right. Thus Rb (group 1) is largest and Be (group Il) is smallest in size. Hence RbCI has greatest, and BeCl, has lowest ionic character. a0, is peroxide of sodium not super oxide, The formula of sodium superoxide is NeO>, ‘Caand CaH, both react with H,O to form H, gas, Ca+2H;0—+ Ca(OH), +H (Cally +2H,0—+ Ca(OH), +2H2 whereas K gives H, while KO, gives O, and H,0, 2K +2H,0 —> 2KOH+H, 2KO2 +2H;0—+2KOH +02 +1309 ‘Similarly, Na gives H, while Na, O, gives H,O, 2Na+2H,0—»2NaOH + Hy NajO3 +.2H,0—>2Na0H+ H,0, Likewise Ba gives H, while BaO, gives H,O, Ba+2H,0—> Ba (Ol), +H, BaO, +2H,0 —> Ba (OF), +H,0, Basic strength ofthe oxides increase in the order Li,0 NaC1>NaBr > Nal, as the sizeof the halide ion increases. The decrease in melting point is due to increase in the covalent character with increase inthe size of anion according to Fajan's rule, 1. @ 2 © 2B. @ 14, @) Zn** + 2NXOH —> 2n(0H)2 +2Na* Za(OH)) +2N8OH —> NayZn0) +2H,0 NayZn0 —» 2Na* +(Zn02)> 1S. ) CaCO) °CO4 4) 7 +C4045) A colourless. B G0 +H,0—>Ca(OH),,.4) Ca(OH), +260) —+Ca(HC0s 5 c Ca HCOs yoy —PCHCO 59) +COr) + HO Correct choice: (b) In Castner Keliner cel, sodium amalgam is formed at ‘mercury cathode, 16. @ 17. @) 3MgeN>—*-9Mp3No: x 7 GP_3371 DPP/ CC10 ——— ft 18, 19. a. 2. 2. Mg3N; + 611;0—»3Mg(OHD),+2NH T Colores) CuSO, +4NH; —[Cu(NH3)4]S05 @ Kand Mg, both form oxides K +0) > K0z:2Mg +0, + 2MgO Mg form nitride also 3Mg++Np > MgsNz K doesnot form nitride. The atom becomes largeron descending the group, 80 the bonds becomes weaker (metallic bond), the cohesive forefenergy decreases and accordingly melting point also decreases, Lesser the tice energy, more will be the solubility in Ho For @ good quality cement, the rato of silica (Si0,) to alumina (Al,O3 should be between 25 and 4 and the ratio af Kime (CaO) to the ttl ofthe oxides of silicon (SiO, aluminium (Al,0,) and iron (Fe,0,) should be a5 close as possible io 2 2Na+2H,0 —>2NaOH +H P 2K +2Hj0-—> 2KOH + Ht All alkali metals decompose water with the evolution of hydrogen, Ca42H,0—+ Ca(OH), +H, t Sr+2Hj,0 —+Sr(OH), +H)? Be +2H0 —> Noreaction Ca, Sr, Ba and Ra decompose cold water readily with evolution of hydrogen. Mg decomposes boiling water but Be is not attacked by water even at high temperatures as its oxidation potential is lower than the other members. Monovalent sodium and potasium ions and divalent ‘magnesium and calcium ions are found in large proportions in biological Huids Alkali metal really lose electron o give monovalent (Mion. Henge theyare neve found in fe tate nature. © @ @ » © © 25, @)_Inalkaline earth metals, ionic size i 2. © © © © creases down the sroup. The lattice energy remains constant because sulphate ion sso larg, sotha small change in etionie size does not make any difference. On moving down the group the degree of hydration of metal ions ‘decreases very much leading to decrease in solubility. BeSO, > MeSO, > C480, >S:S0, > BaSO, ‘The alkali metals dissolve in liquid ammonia without evolution of hydrogen. The metal loses electrons and ‘combine with ammonia molecule. M—5M (in quid ammonia) +¢(ammoniated) M+ (2+y)NH,-9{M(NHL), "+ eH), Hisammoniated electron which responsible for colour, Mgis more red ature than carbon €0,+2Mg>2Mg0+C ‘For Na—)Na* $e" IE) =5.1eV For Na* +¢° —>Na EF=-S.1eV (because the reaction is reverse) Li, =olsatito2e Bondorder= $(4= 2)=1 Lis=oltor1so2s! 1 Bo.=4 2 Lip =2)=05 Par Pe2ear2s! 1 BO.= 54-3) =05 ‘The bond order of Lif and Liz is same but Li} ismore stable than Liz because Li} is smaller in size and has 2 electrons in antibonding orbitals whereas Liz has 3 ‘electrons in antibonding orbitals. Hence Lif is more stable than Lip. DAILY PRACTICE PROBLEMS 1. (b) In Boric acid each B atom is sp” hybridized and contains BO} units which are held together byhydrogen bond. ACI, exists asa dimer(Al,Cl,). Itisa tong Lewis acid asithas an incomplete octet and has a tendency to gain elecons. AICI, undergoes hydrolysis easly and forms an acidic solution, AIC, +3H,0-> AVOH), + 3HCL Opwion()istrue that AICI, slimes at 180%: mate composition of 2 © Magnesia (MgO) Ferricoxide (Fe,0,)=2-3% 4. @_K,S05.Al3(0,)3.24H,0 “> 2K* +480} + 2AI°* + 2611,0 The IE ofGais more than that of Al because of the small stom size and greatar effective nuclear charge of Ga. Ceramicsare inorganic non-metallic, sod mineral. They comeina varity of forms including slcates (ica, SiO, vith metal oxide). onides (oxygen and metals, carbides (Gabon ond metals) aluminate (lumina, AO wih meta odes) and nities The given ceramics are B,C (carbides), SiC (carbides), SiN, (nitrides) and thus, none of these isan oxide. ‘All of these are now atide ceranies, Because they react with water o form methane gas ‘ALC, + 12H,0-——-> 4ANOH), + 3CH, Aluminio carbide Matane Be,C Benim cartie| +4H,0—>2Be(OH), + CH, Metane 8 @) 2Aal+oHCI—™“* 4 2aICl, + 3H 2A1+3Cl, —>2ICls [AL05 +30+3C1 100°C grail, +3C0 vapous cooing Anhydrous AICI, AICI, 6110» ANH; +3HC1+3H0 Ths AIC, cannot be obisined by this method Fused luni (AI,0,) is abd conductor of electric Therefore, colt (Na, AIF and farspar (CaP) ae det purifed alumina which not only make alumina 2 © CHEMISTRY SOLUTIONS 10.) 1L© 12. ®) 13. @) 4 @ 15.@) Pde ea 00d conductor of electricity but also reduce the melting Point ofthe mixtureto around 1140 K. ‘Alum furnishes AI ions which bring about coagulation of negatively charged clay particles, bacteria ete. Due to non-availability of vacant d-orbitals, it cannot ‘exceed its coordination number more than four. Thus carbon never forms complexes e.g.. {Clg} deos not exist but [SiCI, exists. ein = ps Sa Liquid tin (bac (most common and stable) (Rhombic) Although transitions of white to grey tn occurs at any temperature below 15.2°C, it becomes rapid only at 50°C, unless a catalysts present. During the conversion ‘of white tin to grey tin (in cold countries) volume increases. Grey Sn is very britl easily crumbles down to powder. This phenomenon is called tin diseases, tin past. ortin plague. Alz(SOq)s + 6NH4OH — 2AI(OH); +3(NH,) 2504 Al(OH); + NaOH + Na" [A(OH), J Sokublecomplexit is insoluble in NH,OH €0+Ca(OH), CaCO, 1+ H0 a wie CHC054C0,+H30—> Ca(HICO5)2 ace eros Saray ‘Ca(HCO3)) H*** 4 caCO +CO2+ 30 ® ‘and Bare CO3 and CO> Hydrolysis of substituted chlorosilanes yield corresponding silsnols which undergo polymerisation Dialky!silandiol Polymerisation of dialkyl silandiol yields linear thermoplastic polymer. cH, cn, Ho — $i —{6HTiJo —s1—on—> Q on, ch Cty HO— $i— 0 — Sion cH, cH, GP_3371 DPP/CC11 16. @) Ineriness of ns? electrons of the valence shell 10 Cog a cu participate in bonding on moving dowm the group in s Fen pho cme ere era NEN LOSS Asaresult, PUI) ismore stable than PIV) aN: < wa 7 oS Sn(1V)is more stable than So) ; 7 7 be PUAIV) is easly reduced to PHN) and ean acts as an a a cl oxidising agent whereas Sol iseasly oxidise SaV) Na 7 and can acts asa reducing agent 17. © CO, forms carbonic acid H,CO,, when dissolved in o% Ne a water, COisnetrl, whereas other twoGeO3 AndS00; 24.) tn gapitecaoninphyondze ach carbon is thus are sis. linked to thee ober carbon aloms forming hexagonal 18.6) NoB,0, 101,0 4+ NsB,0, rings Since ony three electrons ofeach carbon are used 1NagB,O;—+ 2NaBO; + B03 brio sites aie Cu0+B,0;—> —Cu(BO,), ‘cupric meta bare Bue eed) ore tare 19. 6) HjB0;—C ,Hpo, @C , H2B,0, +Hj0—>2B,03 +H;0 ay Ay, aa? F and Clare more oxidising in nature and can achieve Pb in QV) OS. but Bry and I, can not achieve Pbin (IV) 20.) aK ACI (ime) 21.) OS. secondly ph* is strong in oxidising nature andin 27. (6) its presence, Br~ and I~ can not exis. In SiO, (quartz) each of O-atom is shared between two SiO, ietahedra i ° i Si, 2.@ | i | y o | Oo poe | on 28. @) 23©) 29. (0) 1 Borie acid (HBO, or B -OH) isa ewis acid so(@) is oH incorrect statement. ‘The coordination number exhibited by berylium is 4 and ‘not 6 so statement (b) is incorrect. Both BeCl, and AICI, exhibit bridged structures in solid state so (c) is correct statement, 30. (©) in making hexagonal ring fourth electron of each carbon is free to move. This makes graphite a good conductors ‘of heat and electricity, Further graphite has a two dimensional sheet like structure ‘These various sheets are held together by weak van der ‘Waal's force of atraction. Due to these weak forces of attraction, one layer can slip over the other. This makes eraphite soft and. good lubricating agent. 2Cak, +Si0, + HyS0,—> oye Sif, +H,0+Cas0, DSS, casiry, Glass is a translucent or transparent amorphous supercooled solid solution or we can say super cooled liquid of silicates and borats having a general formula R,O. MO. 6 SiO, where R= Na or Kand M=Ca, Ba, Zn oFPb, ‘The hydrolysis of Trialkylchlorosilane R, SiCl yields dimer: R R R-Si—O—Si—R ‘The linking of identical atoms with each other to form Tong chains is called catenation. However, this property decreases from carbon to lead, Decrease of this property is associated with M-M bond energy which decreases from carbon to lead, ‘Thefeldspars are most abundant aluminosilicate minerals inthe Earth surface. The silicon stoms and aluminium atoms ‘occupy the centres ofinelinked tetrahedra of SiO and [AIO$>. These etahedra connect teach comer to ather techedra forming an ince, three dimesonal. nestvely charged famewerk: The sodium cations st within the vids inthis structure CO, being more dense covers the igniting material more effectively than Ny 2 @ 2 © DAILY PRACTICE PROBLEMS (©) Coloured impurities are removed by adsorbing over 9.) activated charcoal cH, Gn, “cH-C- CH, -CH,0n1 ‘The chemistry ofthe Lassaigne’s test of nitrogen is 10. @ Nar C+N—*9NaCn ‘emp 2NaCN + FeSO4 —> Fe(CN)p +NaSOq Fe(CN), +4NaCN—> Na glFe(CN)] So faroyanide ‘3Nay{Fe(CN)g]+4Fe} —+Feg{Fe(CN)gh+12Na” ere feocanie) ‘Grosian Be) (©) The atom or group which has more power to attract eleetrons in comparision to hydrogen is said to have -I effect. Thus higher the electronegatvity of atom stronger willbe the-Teffect. As electronepativity of N, and Ffollow the order N Gii)> @>Gi). (CH,*CH(OH)COOH as (CH;CH(H)COOH aes" coon) Val, =30K p=725-28- 700 mmole P= 760 mm of Hg at STP) To27K BM RM Vi (Volume of nitrogen at STP) 273x700%40 300760 =33.52mL, Percentage of nitrogen 28x volume of Nz at STP 100 22400 wt. of organie substance 283352100 722400 «0.25 16.76% [Nap(Fe(CN)sNO] +S? > Nay{Fe(CN)sNOS) Sodium tho ivoprsite ‘oie GP_3371 DPP/CC12 14. 15. u. (©) The mixture of sugars is a homogenous one. Homogeneous mixtures ofa solvent and one or more solutes (dissolved substances) are often separated by chromatography. Chromatography works to separate a mixture because the components of a mixture distribute themselves differently when they are in contact with a “two phase system”. One phase is stationary and the other is moving or mobile. The stationary phase may be a solid packed in a tube or a piece of paper. The mobile phase may be liquid of — o) a 18. oy Due to cis-addition of H, to the triple bond, the reduced prodiuct has plane of symmetry and hence i optically inactive. (@ Theamount of s-characterin various hybrid orbitals is as follows. Sp = 50%, sp* = 33% and sp = 25% Therefore s character ofthe C ~ H bond in acetylene (sp) s greater than tha of the C—Hbond in alkene (97? hybridized) which in tum has greater s character of the C= H bond than in alkanes. Thus owing toa high s character ofthe C—H bond in alkynes, the electrons constituting this bond are more strongly held by the carbon nucleus withthe result the hydrogen present fn such a carbon atom can be easily removed as proton. Te acicnature of three types of C- H bonds follows the following order H>-C=C-H>-C-C-H Further, as we know that conjugate base ofa strong acids aweak base, hence the correct order of basicity H-C=C R,C = CH>| orc CH, ‘The correct order of stability of given carbanion is in the order > I> >. R- DPP/CC12 32.9753. .109 =10% 233 0.32 27. (©) Sterioisomerism involve those isomers which contain same ligands in their co-ordination spheres but differ in the arrangement of these ligands in space. Stereo- isomerism is of two type geomerical isomerism and ‘optical isomerism, In geomerical isomerism ligands ‘occupy different positions around the central metal atom oF ion. 26. ®) %ofs In optical isomerism isomers have same formula but differ in their ability to rotate directions ofthe plane of polarised light. Vs CHC, > (CHY,CH > (CHIC recharge -Mefst icy doped Stocales (iewosieet | —eetae seta of soup 29.) Cll =CH-Gier Gti, -CH=EE 4 dae ns formed between C and Cl. Hence itis less reactive dueto 3 6) tetdene flat Spo Cc BS aes 1 wo argos a S24, soss 1 GP_3371 DAILY PRACTICE PROBLEMS (@ A doubly bonded carbon atom having an alkyl group is oxidised to aldehyde which is further oxidised to carboxylic acid. cncrscn = crc, "moO CH,CHO + cH,cH,CHO t+ L cu,CooH cH,CH,CooH 2 @ ® CH,CH; +0S0,0H —> CH;CH,0S0,0H nylon sulphate ‘Addition of sulphuric acid takes place according to Markownikof’sule. Alkanes do not absorb cold cone. H,S0, 3. (© Thegiven molecular formula suggests that the aldehyde formed willbe acetaldehyde hence the alkene willbe CH,CH=CHCH, 2-butene Zalth0 , 2CH,CHO oR ae eth om ot (©) HC-G—CHLBe ANG BrCl = LR ay, cn, ct ot HC-C-cH,-CHy-C-cH, cH, cH, CHEMISTRY SOLUTIONS Phd ea) 6 (@) Electrolysis ofa concentrated aqueous solution ofeither sodium or potassium salts of saturated mono- ‘carboxylic acids yields higher alkane at anode. 2RcooK BSS 42RCOO+ 2K" At anode 2RCOO™ -+ 2RC00+2e° —> R—R+2 2K* +20" 92K 2Kr1g0 RO? ‘At Cathode —— a ae = 281 1st 4 -02,168=92 9. (© CH,CHB:CHB:CH 2"! ,cH,CH=CHCHs ‘Since two bromine atoms are lost from different carbon ‘atom, the reaction is known as B-elimination, . mo Cl str am, Is34| DPP/ CC13 HL. (@) Toluene on oxidation with mild oxidising agent ike 16, (Writing the reaction we get chromyl chloride (CrO,C1) gives benzaldehyte cH, cHo CHMeX+CH;-C=C-H—> coc, CH; —C=CMgX+CH(g) Sowe find that CH, is produced inthis reaction. toluene benzaldehyde ” @ 12. © CHy-CH=CH, +10 48°, cH, -CH-CH, _ te ! . nC oH ast cu, Piet TD onc: cu; cu, tl . a CH; =CH; +H,0 8% cH,-C-cH, TM @ 8CH3—CH=CH, => i 1: rope on Shot ro Addition follows MarkovnikofT rue 2{CH,CH:CH); BOE 13.) The combustion reaction of ethylene is : 6CH,CH,CH,OH + 211,80, CoH +302» 260; +10 Propane! 19, (@) Huckel rules not obeyed. It has only four electrons Both HC==CH and CO, have sp hybridization 14, (©) Weknow that ° Further it does not have continuous conjugation. ico 20, () ~Clgroupiso, p-irectng due to +Reffet; however it eee lemme [eee [ae is deactivating due to strong I effect of CI (fference cH HOH from other o-,p-diecting groups which are activating). M=CH,OH-CH,CI and R = NaHCO; ‘The net result is that chlorobenzene undergoes 0-, p= 15. (¢) Hydration of alkynes give ketones. substitution, but with difficulty oH 1.0.10, HyC-c= cus eS cH I H,C-C-CH, ( 7 ~ aed 1-Butyne NaNH, lig. NH, HyC-CH -C=C~CH, ~CH AECH=8 C—CH, ~ 3-Hexyne (Y) 22, @ Itisastreoselective reaction and in ita trans products formed. Qrewca Se {isa reduction. Metal dissolved reduction [NalC,H,OH reaction is tereo selective} cH, CAs eauiv. BE Be ir Be cA emmy AO |e ee - GP_3371 DPP/ CC13 24, (@) Acetylene reacts with the other three as: ou, ceo eXie csc aa, J" es cHel cis cucl, cata cu LAENOSINHLOH] ARC=CAg + NINO, cama O- 9 beam 2. ©) (Since tertiary carbocation is more stable) 26. HxC- C=C Hs CH,CH. Mec! —> HC C-MgCl + CUCHy lo Oo C=C-CHs 27. (©) Ethene is obtained by electrolysis of dipotassium sucinate a follows a pe cH,cooK cHi,coo 2H,0: 20H” + 2H" Atanode H,COo” GHc00] cy, ~26 > >|] '+2c0, CH,COO” cH,coo] CH nse At cathode 2H" 42° [2H], S35 28. (a) The intermediate 2° carbocation shows resonance: cH, H-CH ty #[erbe-u-crt=cr, ecizr-cr=cn-e1, | 2 sci )Br-CH = CH-CHBe cH,-CH=CH, © Wo HeioAcy, NaBH, CH,-CH-CH, o OH “o — & a ae CU cH; cH ony O ~ MeBr cH,OH cHy cH CHB Methos (1) wil give CHBr CH,br hich is allyic romination, DAILY PRACTICE PROBLEMS High concentration of SO, leads 10 stiffness of flower buds, Radiation coming from sun or outerspace have high energy or short wavelength, which are allowed toenter boy ereen house gases. However, radiation emitted by earths in infrared region, having long wavelength, are reflected back by the envelope of green house gases. 3 @) In cold. water, dissolved oxygen can reach a concentration upto 10 ppm, whereas oxygen in air is about 200, 000 ppm, 4.) Pesticides and synthetic Fertilizers pollute the soil, S.(€) Wateris often treated with Cl, tokill germs. 6 (b) COisa primary pollutant 7. (©) CO and oxides of Nitrogen are poisonous gases present in automobile exhaust gases. & —@) This represents a great step forward for green chemistry, 9 (@) Normal rain water has pH5.6. Thunderstorm results in the formation of NO and HINO, which lowers the pH. 10. (©) The irritant red haze in the traffic and congested places is due to presence of oxides of nitrogen. (©) Photochemical smog is formed in noon in summer. (©) Strength of sewage or degree of water pollution is ‘measured in terms of BOD (Biochemical oxygen demand valve 13. (@) Photochemical smog is caused by oxides of sulphur and nteogen 14. (© Freons and ehorofluorocarbon find their way to stratosphere through without being destroyed in the troposphere due to their low reactivity. In the stratosphere the Cand Bratoms are liberated from the parent compounds by the action of ultraviolet light eg. CRCh + hv —>CRC+ Cl FCI, +hy—+ CPCI, +C1 ‘The Cl atoms can destroy ozone molecules through & variety of catalytic eycles. 1S. (@) Aerosols use CFC and flying jets release NO. Both ‘causes depletion of ozone layer. (©) The ozone layer, existing between 20 to 35 km above the earth's surface, shield the earth from the harmful U. V.radiations from the sun, Depletion of ozone is caused by oxides of nitrogen N,0 +hv —> NON reactive nitric oxide NO+ 0; —+ NO, +0, 16. A 18, 1». BRE RR 2. 29, CHEMISTRY SOLUTIONS @ @ @ © @ ) @ @ © @ @ © © @ phd nek es 03 +h» —+ 0) +0 NO; +0 —> NO+ 0, 203 +hy —> 303 (Netreaction) ‘The presence of oxides of nitrogen increase the decomposition of 03 SCs react with chlorine nitrate and HCI to give HOC and Ch, Using plastic cans for neatly storing substances will not come under green chemistry. The plastic materials are non-biodegradable. Addition of phosphate fertilizers to water leads to nutrient enrichment (eutrophication) ‘Thermal pollution is caused by power plants. Power plant requires a larger quantity of water for cooling. ‘The water after cooling is left in the water body. The temperature of left water is generally very high and affects aquatic life. Based on the features given gas must be SO, Sewage waters purified by micro-organisms. ‘COishighly toxicand impairs respiration. CO combine with haemoglobin of blood and reduces its O, carry capacity ‘Acid rain isthe rain water containing sulphuric acid ‘and nitric acid which are formed from the oxides of sulphur and nitrogen present in the air as pollutants and rain water has a pHrange of 4-5. ‘The oxidised hydrocarbons and ozone in presence of humidity cause photochemical smog. Hydrocarbons + O,, NO,, NO, O, O3 > Peroxides, formaldehyde, peroxyacety/-nitrate (PAN), acrodein et. Hence clorofluorocarbons are not common component ‘of photochemical smog, ‘Microorganisms present in the soil a sink for CO. ‘The ideal value of D.O for growth of fishes is 8 me/ ‘Tmg /t is desirable range, below this value fishes get susceptible to disease. A value of 2 mg/¢ or below is lethal for fishes. ‘The excess of fluorine in water causes fluorosis. The symptoms of fiorosis are mottling of teth (yellowish streaks) and abnormal bones liable to fracture et. Itis an example of endemic disease. Minamata is caused by Hg poisoning. GP_3371 DAILY PRACTICE PROBLEMS © zM @) p= 2M PENA 7a PNA _ 892%6.02x107 «(362)3 x10" M 6355 thas fee uniteell © (02°21, ( 3 y @y 2 Aas) “2 Writes ce centred bie suc ‘Zn** ion is attached to four $*- ions and each S* remains in contact with four Zn? ions. Hence coordination numberof ech oni 6 (©) The increase in pressure results in decrease in size of 4 Og s @ jons (more in case of anion than cation), the r* /¢ increases and the coordination number also increase, 7. @) & raiois SF = 0.44, Hence LiF has Nat structure with CN=6. 8 (@)_ Diamond istike ZnS. In diamond cubic unit cell, there are eight comer atoms, sx face centered atoms and four more atoms inside the structure. Namber of atoms present in a diamond cubic cell tye: ar? 2 (comers) (face (inside centered) body) (a) Fraction of unoccupied sites in NaCl crystal 2.165%10° 2.178410" =8 +4e8 178" 105 ~ 2.165 “108 _ 0.13 "10° 2.178" 10° 2.178 PO 2596. 103 2178 ~996* (@) MnO, © 10 @ @) 1. (@) Its the property of liquid crystal 1S. @ Togetan—type semiconductor from silicon, bbe doped with a substance with valency 5. ce. silicon is doped with phosphorus to form a n= type semiconductor. 16. @ m=2dsind; should 8 2x1A=2xdsin=>d=115A : [n0-3} CHEMISTRY SOLUTIONS Phd ed es) 7. @ 2M 18. @ p ee N, 2x27 6.0210 «(4.05) «10 Hence it is face centred cubic unit lattice. Again 4r= ay2 =5.727A r= 1432 BO das ae Hence gy =I, 439 20, (€) Forcubic geometry the limiting ratiois 20.731 ie. (0 21, (@) Statement (a) iscorrect, 22. (@)_ For bcc lattice body diagonal = a3. ‘The distance between the two oppositely charged ions =48 2 BTA 359m 23, @ Number of formulas in cube shaped crystals 10 33 = £9 .6,02%1073 since in NaCl type of structure 4 585 MPs formula units form'a’ cell nites = 1.0%6.0210? 2 575 107 unital S85x4 24. (©) As CsClis body-centred, d = V3a/2. 25. (€) ABisjust like NaCI. Thus twelve’ are at edges and | within body offec Le. in octahedral voids and six Brat faces and 8 at corner. Among the given crystals, only silicon exists as a covalent solid. thas diamond like structure. 27. (¢) The pf. for body centred cube = 0.68 see text), 26. 28, @) Cabsebe tot ge inking wend ‘consult the table, All are correct. v. © 30. () In Na,0 there is antfluorte structure. Here negative jons form the cep arrangement so that each positive n is surrounded by 4 negative ions and each negative jon is surrounded by 8 positive ions. So coordination no, of Na* is 4 DAILY PRACTICE PROBLEMS 1.) According toLe-chatelers principle, foran exothermic reaction (AH< 0) increase in temperature decreases the solubility 2) Prout = PA *Xa + Phx RB = 80.004 + 120.00.6= 104mm Hg ‘The observed Py) is 100 mam Hg which is less than 104 mm Hg. Hence the solution shows negative deviation, 3. (©) Pa= phxxy= Total pressure x yq Pp = phxxq =Total pressure yy, ‘Where x and y represent mole fraction in liquid and ‘vapour phase respectively. 4 KW, 1000 My Wa 1.86% Wy 1000 25000 Wp =508 ‘The amount used shouldbe more than 50g. Sq) AVenRT= RT or My (et Where M, and m, molecular mass of solute mass of solute CHEMISTRY SOLUTIONS 6 10. a. 2. phd sneaks) (@ According to Henry's lav, m=kxp given Ky= 14x 10 Po, =05 or (©) Leta. be the give of dissociation then ae weer Van’tHofts factori= 1848+ 14 q T Again Van't Hoff’ factor Normal mol.wt _ 585 _) g5 Observed molwt 31.8 Equating to both values of, 1 ¢@-=1.83 a= 083 (€) These two components A and B follows the condition cof Raoult’ law ifthe force of attraction between Aand Bis equal tothe force of attraction between A.and A or BandB. (©). There is no change in vapour pressure, ®) p= xa(Ph PB) + PSE Pe = PAXKa~ PB Xa +P: P,=PA*Xq— PHC Xp)+ PS Ps = DA Xy +h Xp. ‘This is condition for ideal solution. @ AT,=0-.000732%) = 0.00732 AT =ix Ky at 0.00732 Kyxm 1.860.002 © GP_3371 DPP/ CC16 -— AA Hrd 16. aw. 18, 1. 20. eo 2. © 5) © @ © => [Af =100.18-100=0.18°C] 1.86 asia -984"C As the Freezing Point of pure water is 0% = 0.18% ‘Thu the freezing point of solution will be -0.654°C. (OH ix < 0 (CHgLand C,H,OH form non-ideal solution. For this solution intermolecular interactions between ‘heptane and ethanol are weaker than n-heptane-n- heptane & ethanol-ethanol interactions hence the solution of n-heptane and ethanol is non-ideal and shows positive deviation from Raoult’s law. Liquid solvent and solid solvent are in equilibrium, ‘The molality involves weights of the solute and the solvent. Since weight does not change with the temperature, therefore molality does not depend upon the temperature, © @ 00 swt. of 70% acid = O31. 70 = 45 gm ‘Vant Hoff factor = 4in ease of (NH,);PO,. (NH,),PO, —=* 3NHi+ POP AT, =iKm Given, (ATyc> (AT py ig Kym>iykym (kis same for same solvent) So, x isundergoing dissociation in water. 1= we Depression in FP. cc No. of particles. ‘Al,(S04)3 provides five ions on ionisation Alz($04);—92A1"* +3803 while KC provides two ions KcI==k* +r" 29, © @ © © @ @ @ CeHy:0gandC; HO, ar€ not ionized sothey have single particle. Hence, Al{SO,); have maximum value of depression in Por lowest EP Sodium sulphate dissociates as ‘Na;SO4(s)—>2Na* +50, thence van"t hoff factor = 3 Now AT, = iky.m =3% 186.001 =00558K K4[Fe(CN)g] and Aly($0,)5 both dissociates to sive Sions ori=5 K,(Fe(CN),) == 4K" + {Fe(CN) I and Aly(SO4)3—==2A0* + 380,77 1 mola solution means 1 mole of solute dissolved in 1000 gm solvent =1 Pe roe = 10008 Des =55.56 Bw Xsaue= [pau =00177 Concentration of a =0.955M Ia" [co¥]=o955m Azeotrope of HCI + H,O contains 20.2% HCL AT; =i.kym3 AT, =iky.n 0.985 =1.91M. at, atk A; = 0-(-0.186C)=0.186C 0.186 186 0152401186 288686, a, a DSEAOIBS 0052 Mole fraction of any component A. No.of moles of A Total No. of moles As otal no, of moles > no, of moles of A thus x can never be equal o one or zero. Pn DAILY PRACTICE PROBLEMS (©) Conductivity ofan electrolyte depends on the mobility of ions and concentration of ions. The motion of an ionic species in an electric field is retarded by the oppositely charged ions due to their interionic attraction. On dilution, concentration of electrolyte decreases and the retarding influence of oppositely charged ions decreases. Therefore mobility of ions @)_ Degree of dissociation, A 80 10? 00 2 K, = £2 aca? = 4x (2x10) ao n =1.25x10% (©) HCl completely dissociates to give H® and CI” ions, hhence act as very good electrolyte. While others are non- electrolytes G@) AG=-nFE® @ (@) AQ=57+73=130Sem*mot (@ Koblrausch’s Law states that at infinite dilution, each ion migrates independently of its co-ion and contributes to the total equivalent conductance of an electrolyte a definite share which depends only on its From this definition we can see that option (d) is the correct answer. (©) Writing the equation for pentane-oxygen fuel cell at respective electrodes and overall reaction, we get At Anode: 296500 1.1) =2123W. C.Hy +100 -> SCO, +32H" +326" ee) ‘AtCathode: 80, +3211 +322" 16H,0 Overall:CH,, +80, 500, +6H,0 Calculation of AG® for the above reaction AG? =[Sx(-3944) +6 -237.2)] 82) = 1972.0- 1423.2 +82 =~ 3387.01) 3387000 Joules. From the equation we find n= 32 Using the relation, AG® various values, we get ~ NPE; and substivting 3387000 =-32+96500% £2, 4 (F=96500C) CHEMISTRY SOLUTIONS phd en ot Eo 3296500 3387000 3387 ~ 3088000 % 3088 ‘Thus option (6) is correct answer Standard Gibbs free energyis given as AG HE 0 Forther AG° =-RT'InK, AG? >and Ky <1 10, @) Fe? Ves B=-048 Fe /Re!?; E=0.77 The metal having higher negative electrode potential values can displace metals having lower values of negative lecrode potential from ther sl solutions, 1, @ Wa_Ws, 16 Woot Ag V=1,0968V NEF E, Ey’ 8 108 Weof Ag=21.6 8 12. (@) Esa = Es cate)” Ein anatey 3 13. (© CH,OH()+ 50,(@)-> C0, (@) +2400) AG, = (AG; (COp,g)+24G_(H0,0)— 394.4+2(-237.2)-(-1662)—0 394,4-474.4 + 166.2=~702.6kI +100 =9796 4 Init, T,n and Fare constant So Bis based upon In C2 /Cy RT, aPx®T inc /¢, ap ine2/C1 RTInCyC, Atconstant temperature AG is based upon In (C/C)). ae (Since 22400 ml at STP 1S. @) 112mloftatstP= 2218 =Mawt) GP_3371 DPP/ CC17 —— htt steg = Eawtxixt ‘Amount deposi ‘96500 2xL12 _1x965xi 2400 ~ 96500 * i=lamp 16. @) ForZn®* Zn a 0) e 230387 5 ‘aaa P12 la] E 2+ pq 7-079 17. (@) The given order of reduction potentials (or tendencies) is Z > Y > X. A spontaneous reaction will have the following characteristics Zreduced and Y oxidised Zreduced and X oxidised Y reduced and X oxidised Hence, ¥ will oxidise X and not, 18, () For, Mé +X” —9M+X, Ely =044-033=011V is positive, hence reaction is spontaneous, Min 19. @) will oxidise C- mn according tothe equation 2Mn0; + 16H" + 10C” —+2Mn** +8H,0+5C1, P The cell corresponding to this reaction is as follows: Pr, C1y (atm (CT Mog Mi"? | Pe Ey = L51-140=0.11V fy being +ve, AG® will be -ve and hence the above reaction is feasible. MnO will not only oxidise Fe?* ion but also CI” ion simultaneously. 20, (¢) The ell reaction isa follows: rovers Bees Adding A+B A+B 24, (b) Conductivity (X) = conductance (c) x cell constant x +, Cell constant condusivigernwon= 2 X 7, 1000 _ XZ j96 ma =X 2100 _ XZ 1g Am (NaOH) = 2x9 = 22, (©) From the given data we find Fe isstrongest oxidising agent. More the positive value of E°, more is the tendency o get oxidized. Thus correct option is(c). 23, (€) Atinfinit dilution each ion makes definite contribution towards molar conductance which is given by Ag ay hy teh 24, (@) In case of equivalent conductance of strong electrolyte theres litle increase with dilution, 25. (@) A device that converts energy of combustion of fuels, “directly into electrical energy is known as fuel cel. 0.0592, (Mn™*] 2 We 26. @ aqua 0.05924 Mn") 2 oy = E°=0.0592%2 (ogi Mn?" « ptt) AE= Ey~E, = 0105922(pH ~pH,) =0.118%1 o18v 27. @ Heren=4,and[H"]=10"3(aspH=3) Applying Nernst equation ap - 2959 jog FET n ToD 352 147-995 p 00° 4 0*)* x0. oss 8 oet07 1.67- 2°? fogi0! = 1.67-0.103= 1.567 4 28. (b) In Hy ~Oy fuel cell, the combustion of H, occurs 10 ‘create potential difference between the two electrodes 2» @ 30. (@) Hy — 2H 426° Laxm 10% 2 59, (10 yy? <0 202g (37) By? =059V L 6 DAILY PRACTICE PROBLEMS © @ © © © © eae Bit 1 Ro logk= log A- 2 BES BAS 03K T L Plotof og kV. -E, 2303R Rate constant k= 0.6 x 10-* mole per second. unit mol 11S" shows zero order reaction) Fora zero order reaction IAI=IAly—kt 8% and [Ag]-IAl 506 10"? x20x60=072M. Straightline Slo tae Where isthe order ofreaction 9. 7 2 (0 Lay aro) @ 2°G n=2 Let x torr of CH,O decompose after 20 min. Then, 802+ 2x=120 x =40 torr = 50% of initial pressure. Hence t= 20 min. For 75% reaction, fraction left 3-1 10 ~ 100-4 (2, Wa ft ves 2 Tine ete fr 75 ection, Sacaan Topstar om nc he ped Sten weg th coy bea Se pats tlm wiewersciedarensag a ean + catalyst Propres of easton —> a Here E, is the threshold energy. E,andE,, is energy of activation ofreaction in absence 43, and presence of catalyst respectively. 2" (yan (a), 120 4a Guar CHEMISTRY SOLUTIONS phd haa) (©) Fora first order reaction ©) Rate Rate = k{2C, [4g I* = 4x21C,PICgI* (@) A(g)+2B—@)—>C@)+D@) Rate = KAI]? = k(0.60)(0.80)* a when p, = 0.20 atm p, is reduced to 0.40 and Pp =0.40 (See stoichiometric representation) Rate=K{0.40] (0.407. “a, 0.40%0.40%0.40_ 1 0.60%0.800.80 6 (@) From data 1 and 3, iti clear that keeping (B) const, When [A] is doubled, rate remains unaffected. Hence rate is independent of [A]. from 1 and 4, keeping [A] constant, when [B] is doubled, rate become 8 times. Hence rate ce [BP. (a) Since intial velocity is ten times the permissible value Ay=I0A Gi divide by (= , tog ht. - 2303, 100 we PRA 0695/30" A 2.303430 1og10 = 100 days. (a) Presence of catalyst does not affect enthalpy change of reaction AHy =E; Ey = 180-200=~20 mol (@ Since the stow step is the rate determining step hence if we consider option (A) we find Rate= &{C][ 11,5] GP_3371 DPP/ CC18 ———— sl [Now if we consider option (B) we find 16. Fora first order reaction 0.693, , 0.69 1 Rate= &{Ch][ HS Afi) tugs pt R= ogg 205 x 10-557 For equation, 2303, 4 HS == Ht + HS- 1 © ta “E83 - 2308 (91082-l0g3) k 8. be) rate= afc} 25] Thus slow step should involve | molecule of Cl, and 1 molecule of HS. hence only, mechanism (A) is consistent with the given on rate equation int 14, @ From 1 and 2! sets of data - no change in rate is & observed with the change in concentration of C°.So 19. @) Overall oder = sum of orders wir. each reactant. the order with respect to "Cis ero. Letthe order be x and y for G and H respectively From 1 and 4! ses of data Dividing eg. (4) byeg.(1) 1 10? [ost sox10™ L010 01025 = (0.5) or0.5=05 2x22 Lae ene eeAiee mente ease += For(1) and (3), therateis doubled when cone. of sets of data dividing eg. (1) by e4. 3) Gis doubled keeping that of Hconstant ie. rate [6] <= 5.0x1 + [2] From (2)and(3), y=2 10x10 [0.010 Overall orders 3. (05)'=05y > y=1 20. (@) Rate, =KIAPIBI": Rate,=k2AP EB)" “The order with respect to "Bis Rae, Kart" Sothe order with respective the reactants A, Band Cis ey MAPIBI" 2,1 and0. =PR(an=2.24 18. @) AH =Exir) —Exioy 20 ‘Thus energy of activation for reverse reaction depend 24. oe ‘upon whether reaction is exothermic or endothermic reaction is exothermic, AH=—ve Ey) > Exe) reaction is endothermic AH =+¥e Ey) whose -E, 2303R ‘When concentration of Ais doubled, rate is doubled. Hence order with respect to A is one. slope is 2. 29, © © @ When concentrations of both A and B are doubled, rateincreaes by 8 times hence order with respect B is2. rate=K(AT BPE 2N205 > 4NO, +0 From the unit ofrate constant itscear thatthe reaction follow first order kinetics. Hence by rate law equation, = KIN,O,] where = 1.02% 104, 4=34 «102 1.02<104=3.4 10 (N,0,) (N,0,]=3M “Third order If we write rat of reaction in terms of concentration of NH, and H,,then Rate ofeaction =} SUNH3] __1 dltta) 2 a@ 3 a so, 4NHa) 2 alti} dt a Exerny * Exon E,can be calculated, Forreaction 3A» B+ Ifitis zero order reaction r=K[A?, Lethe rate remains sameat any concentration of ‘A. Le independent upon ‘concentration of A, 2.308, 1 _ 2.303 2303 jog 4 = 2308 aon os Ty a8 GP_3371 DAILY PRACTICE PROBLEMS (Siler the charge on anion, lesser wl be its canulingponer Kr hve Br wh es charge of—1 on Br hs iar temtcaeinein camping FAO, © 0) @ ©) According French equation Zc pl on Empl" or log = logkp"" or log + = logk + Log p (©) I micron j= 10-%mand 1 millimicron = 107m. @ Allareirreversible colloidal systems. (@ Cetytrimethyl ammoniumromide, [CigH33(CHs)3N*Br] isa cationiemicelle ) o- Polarhead 1m Non-polar tail (micelle) 10, (€) Itis duetoimpact of molecules of dispersion medium on u. the colloidal particles © 12, (¢) The movement towards anode shows that sol is negative. 1B. 4. 18, 16. 1. For coagulation of negative sol. Cation with higher chargeis more effective, (@)_ Fe(OH), is postive sol. K,{Fe(CN),] will provide [Fe(CN),1* for coagulation (©) Alum, coagulates mud particles and helps in purifying wate, (a) On increasing temperature adsorption of a gas on surface of solid decreases. Solid adsorb greater amount of substances at lower temperature, For physiosorption the 4 H valueis 10-40 kJ/mol On shaking with the dispersion medium, colloids directly form the colloidal sol. Hence they are called intrinsic colloids... glue. (@ According toFreundlich adsorption isotherm. At intermediate pressure, extent of adsorption © @ 19. BRE 2. 2. CHEMISTRY SOLUTIONS plotof tog vs tog Pis linear with stope = @ © ) @ @ © @ © @ @ © DPP/CC19 xm P L ‘Tannin used in leather industry contains negatively ‘charged colloidal particles. ‘When oppositely charged sols are mixed their charges are neutralised. Both sols may be partially or completely precipitated According toLangmuit's model of adsorption of gas na soild surface the mass of gas adsorbed(x)per gram of the adsorbent (m) is directly proportional 0 the pressure of the gas (p) at constant temperature i.e. cp “The mare the liquefiable nature ofa gas, the moreis the ‘enthalpy of adsorption, Water is more liquefiable. ‘A catalyst speeds up both forward and backward reaction with the same rate. ‘So, equilibrium constant is not affected by the presence ‘of a catalyst at any given temperature. As Sb,S, is a negative sl, so Al,(SO,), will be the ‘most effective coagulant due to higher postive charge ‘on Al (Al**)~Hardy-Schulze rule Athigh pressure the extent of adsorption follows zero order kinetics. ‘The critical micelle concentration is the lowest ‘concentration at which micelle formation appears ‘When surfactants are present above that CMC, they ‘can act as emulsifiers that will solubilise a compound ‘which is normally insoluble in the solvent being used. 30. (b) Peptisation i disintegration of colloidal aggregate Reha eD * 2 1B M4 16. vw. DAILY PRACTICE PROBLEMS (2) Theconversion of metal sulphide tometal oxideinvolves the process of roasting (i.e, xis roasting) ‘Themetal oxides can then be converted toimpure metal by reduction. Of the given choices in (a) and (b) the reduction processisthat ofsmelting,(.e,)*issmelting) “The conversion of impure metal to pure metal involves a process of purification, Thus itis electrolysis. © © © © (a) Dalomite on calcination gives CaO, MgO which provides basic lining in furnace, © (©) Zabeing more reactive than Ag and Au, displaces them. 4Ag + 8NACN +2H,0+ 0, —Lessting 4NalAg(CN))]+4NSOH Soluble Sodium dcyaoargenate() ‘Soluble cyanide compound can be treated with Zn to ‘give metal by displacement. 2NaLAg(CN),] +Zn _ Dispose. Nag(2n(CN)4] +2Agh (@ Decomposition of carbonates and hydrated oxides. © (©) Pigironorcast iron contains 3~5% carbon and varying amounts of Mn, Si, Pand S which makes the iron hard and brite (©) Cupriteis Cu,Oand Argentiteis Ag,S: (©) Cyanide process is for gold (ID); floatation process - pine oil (-B); Electrolytic reduction Al (ILC); Zone refining -Ge (V-A), (©) Fora spontaneous reaction , A G* must be negative and it can be possible nly in this case when x €Cu +80) (@) Zone refiningis based on the difference in solubility of impurities in molten and solid state of the meta. This method is used for obtaining metals of very high purity, ©) The reactions involved in cyanide extraction process AgyS_ + 4NaCN > 2Na[Ag(CN),}+Na,S (argent) 4Na,$+ 502 +2H,0 ->2Na,S0,+4NaOH +28 oxiaing wort ANAL AKKCN 4] 20, PNBg(ZCN)] +2AB (redining ‘agen ©) 1,0, cannot be reduced by carbon. @ (©) The given reaction isthe method named as Van Arkel forthe purification of titanium (©) CaandK are strong reducing agents, hence their oxides ‘cannot be reduced with carbon (©) ZrandT are purified by van Arkel method. Ze(s)+ 21g(g) —> Zsl4(@) 2g) OU 52942148) 26. (€) (ii)and (iv) reactions occur inthe temperaturerange of 2». 30, 900 — 150K in blast furnace. (@ Zinciteis Zn0, (a) FeO is capable forming slag with SiO, Si) +FeO + FeSiO3 @ (©) ‘The two equation are: a4s.40,0)-»2a, 0,6 446° 28 ma o eqn. 0)» 26404, 846"= S00 ma! @ ‘Subtracting equation (i) from equation (i) we have, 4 array 2 Aare +2en0.0), FAlOd+ FCO). 2 1,0366)+ £0069, ,6°= 28710 mor! GP_3371 6. 1 & 10, u. 2, 1B. 14 18. 16. 17. 18, 1». DAILY PRACTICE PROBLEMS ) © © @ © ee co) @ © © © © © © © Hypophosphorous acid is H,PO, in which OS. of Pis al ‘The bond angle decreases on moving down the group due to decrease in bond pair-bond pair repulsion. NH, PH, AsH, SoH, BH, a This can also be explained bythe fact tha asthe size of central atom increases sp? hybrid orbital becomes more distint with inreasing size of central atom ie pre p-orbitals are utilized in M-H bonding. CuSO, +4NH3 > [Cu(NH3)4]80, BHoecompler dno Cut 3* ‘Thenitroprussdeionis (Fe(CN),NO"}*. The magnetic moment measurements reveal the presence of 4 "unpaired electrons in Fe which must be then in Fe"* Gal and not Fe" Ge) [Fe(H,0),NO} ions formed 4HCI+0, -» 2C1, +240 {ir oad of white fumes 10, Thehybrdsaion is 3(7#7 40-0) Tsp) ‘Dueto large enthalpy of vaporisation SO, can be used asrefrigerant Oxides which are more ionic in nature (salt like) are known assaline oxidese.g. oxides of alkali metals Among the given compounds, the NH is most ba- sic, Hence has highest proton affinity ‘Helium is heavier than hydrogen although itis non- inflammable tis H,S0, oH HO- P-H it can form two series of salts by i 8 replacement of H attached to oxygen RCOO is not pseudo halide. In gaseous state the HClis covalent in nature while in aqueous solution it ionises to give HY and Ci ions H i ‘Hypophosphorous acid H-O- P->0 | H ‘Two H-atoms are attached to Patom. uring disproportionation same compound undergo simultaneous oxidation and reduction, CHEMISTRY SOLUTIONS 20. ©) a © 2 © B® mo 25.) 26. @) 7. © 23. @ 2. 30. @ phd he7 4 _ oe poe oe arn eee ee paazeo-coc! caer ® AGO Aad I, U0 br ‘ ee een eee eae eaneed Soo; Suaoaa ieeeut nataeces ct ee eee aes a ee eee or Fame re Peay ees situated on the plane and the top and bottom, clo, 28,07 +1, > 8409 +20" Texathionate FeS0,.7H,0 > FeSO, +7H,0 2FeSO4—*> Fez03 +80) +805 HOC! V,0, + SO, 2V,0,+0,->2V,05 According to their positions n the periods, these values aren the order: Yo" K,Cr,0,+ 2KNO, + H,O Hence Cr,0;- and H,0 are formed. Mn2* (dis more stable than Ma** (ct), thus ‘Mai imin2e =F in,0, <=""—[KMQ04]-==— [Mn0,}" MnO, ‘ON. of Ct in all the species is +6, Configuration of Cr (VDis(As) 34°. Hence no d-d electron transition. ‘The number of unpaired electrons in Ni?*(aq) =2 ‘Water is weak ligand hence no pairing will ake place spin magnetic moment = Yikn-+2) = 222) Ma’ =fi=282 2€u30+Cu;8 —> 600 +80 se retain Eu has electron configuration [Xe]4f7 hence stable die to half filled atomic orbitals CHEMISTRY SOLUTIONS DPP/CC22 15. ABNOy->AG0N05 10 16. (@) 17.0) 2ABNO3 +NayS;03 > Ag7S,03 +2NaNO} ‘Oxidation of water takes place in presence of Mn in biological process 18. @ (@) -V=3d345?; V2 =349 = 3 unpaired electrons (Cr=345 ds! C12" = 3a = 4 unpaired electrons ‘Mn =3d5 4s?; Mn2* = 3d = $ unpaired electrons Fe=3d6 4s? Fe2* = 3464 unpaired electrons Hence the correct order of paramagnetic behaviour V2" Ret*>Cot* >Nit* (©) In solution, the stability of the compound depends upon electrode potentials, SEP ofthe transitions metal ions are given as 197, Fe /Fe= 40.77; (0.41, Se > is highly stable as it does not show+20.5. @ Se-O-2),6¢3) T-62,63,64) CHEDDAR.) Mn—(4 2), 34 (4 4). 5) 604-7) ie. Se K,0, + Mn,0,, +;0 Explosive 2 © ‘AgCi(s)+ 2NHLOH (aq) [Ae (NHS), Jev(ag)+2820(1) 23. (@)_Paramagnetic momentisclrectly proportional conumber ‘of unpaired electrons present in the complex. GP_3371 DPP/ CC22 ———— as 26, (€) Parke's process Itis for extraction of silver 24, @ d3— strong ligand field te & nennt2 = 3 =1.73BM weak as wellasin strong ld n=V38) = Vi5 =387BM. tin weak ligand field i 1 » 24 =439 din strong ligand field i f te 7 n=V2@) = VB =282. 25, (b)_Inneutral or faintly alkaline medium thiosulphate is quantitatively oxidized by KMnO, to SO, SKMn0, +-3Na,8,0, + H,0—> 3K;S0, + 8MnO, + 3Na,SO, + 2KOH 2. 28, 28. @ ) . (a) © (Cu, Hg and Ag are attacked by conc acids but gold is notattacked, AUC; forms H[AUCI,] acomples with HC which is used for toning in photography: Nin +H" (acidmedium) = Sit, When KI is added tomercutie iodide it dissslvein it and frm complex. Hgly +KI® KylHely] seco ‘Cobb ei) ‘On heating High decomposes as Hel, ig+ Ip (violet vapour) other has — ve Ef» Cat 1c EAN Be Fete 9. 10. 2 DAILY PRACTICE PROBLEMS © © @ @ © © @ © @ @ ‘According to specrochemical series C,0}- >F- CCN is coordinated to cobalt as the ligand and conednated compounds have diffrent properties than the individual species INiX,)?, the electronic configuration of Ni 3d contains two unpaired electrons and the hybridisation is sp* (etrahedral), ‘The erystal field spliting in tetrahedral complexes is ower than that in octahedral complexes, and 4 =~ Sao. [Co(NH,},CO,ICIO, Six monodentate ligands are attached to Cohence C.N. of Co= 6: OLN.=x4+5%(O)+ 1x (2)+ CN=0 2. x= 43; electronic configuration of Co™{Ar) 34*4s? hence numberof delectrons is 6. All d electrons are paired is diamagnetic in nature ‘Ti(C)H) is an organometallic compound due to Ti directly attached to C- atom ‘Tetraethyl lead Pb(C,H,), is not xbonded complex. It is o bonded organometallic compound CoC, .6NH; —>x™ 26I56 xCI- +AgNO, —x age “he ‘Number of moles of the complex 2.615 Jorg 7001 moles ‘Number of moles of AgCl obtained CHEMISTRY SOLUTIONS DPP/CC23 No, of moles of AgCl obtained =3 xNo. ofmoles of complex 0.03 "O01 13, (@) ‘The chemical formula of Pentaminenitrochromium (1) chlorideis [cx(1sH:),NO Jc It can exist in following two structures [Cce(nstts),NO, Jel, and [[cr(NH3),0NO |e, Therefore the type of isomerism found in this ‘compounds linkage isomerism as nitro groupis linked through N as -NO, o through O as -ONO. Nickel ions are frequently detected bythe formation of ted precipitate of the complex of nickel Agel (ppt) (©) ‘The correc JUPAC Name ofMa(CN) Pentacyanomangnate (I) @) [NL wwi,p- CECE ice, no of unpaired electron =2 hybridization - sp » (©) In [CKCO),NH,|* CO is bonded to cobalt through and xbonding. K,[Ni(EDTA)], Since EDTA is hexadentate and chelating and coordinates from six sides forming more stable complex. @ eae 9 10. DAILY PRACTICE PROBLEMS © CHEMISTRY SOLUTIONS 12 (© HOH doesnot undergo norm eaton, al hes DPP/CC24 Newer 1. 0) GpD>C=0 + CHLCHMEBr—$> O-: Ontia — d ea bys 5: meyers eat DS oc OMBE oe Sateen cH > CCen.cn, a @ @ @ @ ® © @ @ OOS ‘a cin, rier lng ra oh gh . ww onftacsma flay ees formece-y -Clis o, p-tirecting. ale 80 ace, HEN ox, Co Zs =o" {fener orl [Nuclear substitution will not take place. 5. 0) The compound has two similar assymmetric cH, (C-atoms. It has plane of symmetry and exist in meso ow Se cy a 16. © res? + a cna cna, Ch cal, Qh, tn 17. (@) Tres characer onthe ore — Gigcooks Coors ios CksoM Fitba crt en log ede oe, ont ox GHyC00 eco coe. Fae crnge cid the sek the jose ees OL, 0b) Renton evezn ly aie a ald nd stom in presence of ether is known as Wurtz fitting reaction GP_3371 1. a. 2. DPP/ CC24 $53 CH,CL + 2Na-+C1CH, —> CglIgCHy +2NaCI ci, Tone an t 28. @ Cell +CH,CH,CH,C— "> Cyt, Catchy a 0 oops tee (© 2C1-C-CHy +6Ag CHC =CCH,+6AKC 26. (€) NO, group withdraws electrons from o- and p- 4 ne posts wlbeer aver el yess ion towards nucleophilic substation, 1.1, 1atichlorothane Ls a ©) Compound which are mirorimage ofeach other and 27, (@)CqHsCOOAG + Br, Hasse mason enon superimpossble are termed as enantiomers. 1, cn, CglisBr+CO, + AgBr " oH Ho. u Ho 1 dy on YiCH)2 &, a % «9 cmp n a(S) sua ‘These re enantiomers (@ Todor tests given by meth ketones, acetaldehyde and methyl secondary alcohols 2. @CC-CH,CHy + KOH ciy—cH—cH,—on (OHyC-CHCH, +3KC1 cH, Isobuty alcohol is primary alcohol hence doesnt sive positive iodoform tes. _Alckow_, © BrCH,-CH,Br SSK, cH, CHB ° i Nant cH,CH,C-o# Ne CH=CH hs liminationaf Be fron Cl=CHBrreqiesastonger 30. (@) A song nucleophile favours the Sy? reaction anda tune becuse here, Br soqizes parti double and weak nucleophile favours the St teation, character due to resonance. First reaction is Sy reaction because C;H,OHisused (© C@HsCHCH,Br being an optically ative secondary as solvent which sa weak nucleophile aly bromide undergoes 5,3 nucleophilic substitution ‘Seoond reaction is $,2 reaction because C,H,O- is reaction. Hence it undergoes complete inversion of strong nucleophile. configuration i i cated pre r Ms beats HEC CH, (© Chioralonrescton wit chlorobenzene inthe presence of a catalytic amount of sulphuric acid forms DDT. ichlorodipheny! Trichloro ethane). 4 <_\-a 1 elo — tt S-a ca AS O- DAILY PRACTICE PROBLEMS 1. (@) Lucas reagentiscone, HCI + anhyd. ZnCl, 2 © 3. (@) Methyl alcohol (CH,OH)is alsoknown as.carbinol, Hence vinyl carbinol is CH, = CH -CH,OH 4. (@) methyl pentanol-3 will be dehydrated most readily Sinceit preuces tertiary carbonium ion as intermedi ke cH, cH, cy . i sen, -cit;-¢ ~cry~cHs $ 5 © Z © Ga—tucH,c 7. @ 2-Phenylethanol, CeHsCH,CH,OH, is a 1° alcohol ‘hich can be prepared from C,H,MgBr by treating with ethylene oxide note that HCHO will introduce only one carbon atom, ie. it will give C,H,CH,OH and not (CoH,CH,CH,OFD. CoHlsMgBr+ 7°. —scHtsCH,CH,0H + Cl1sMgBr + HCHO—>C,H1sCH,0H 8.) Methyl vinyl ether under anhydrous condition at room, temperature undergoes addition reaction, city cH-oct—#"5.cH, -cH-O-CHy } be 9) Tertiary alcohols react fastest with conc. HCI and anhydrous ZnCl, (lucas reagent) as its mechanism proceeds through the formation of stable tertiary carbocation, ‘Mechanism ts eee ere oer cH, 2 Met! Propn-2-1 = (CH,),C— On, +cr CHEMISTRY SOLUTIONS DPP/CC25 Step2: (CHs),C-OHy == (CH),C* +H,0 ¥°Cuosaton Step3: (CHy)C* +C —=(CHy),C-Cl "Bele 10. @ The two components should be (CH,),CONa + (CH,),CBr However, tert-alky halides tend undergo cH; cH; CHj—C=CH, ‘mat peop oH OH OH 1H, coon 6. @ Electron releasing groups (~CH, OCH, NCH, ete) intensify the negative charge of phenoxide ion, Le., destablises it hence decrease ionization of parent phenol, Therefore decreases acidity while electron ‘donating groups (-NO;,-COOH, -CHO etc.) increases acidity 16. (b) Number of active hydrogen in a compound corresponds to the number of moles of CH, evolved per mole of the ‘compound, NH, SH, ~ OH or -C= CHEM cr Hy + (2CHgfrom— NH) GP_3371 DPP/ CC25 S551 IT.(b) 2B. b) 18.(b) 24, (@) The commercial alcohol is made unfit for drinking by mixing in it some copper sulphate (to give it colour) ONa and pyridine (afoul smelling liquid). Itis known as vw. @ CO, —> ‘denaturation of alcoho Soudan 25.) CHCH,CH,CH,oH 28H, cH,cH,cH;CHO Phenoxide omoct, 26, @ CHy——Sc-cH, EG H,c-¢-cH i i Hy cH; 21. (© Electron withirawing group sabiliss the benzene rng [ecrscor0 ‘due to delocaisation of charge. CH and -CH,OH are electron donating group and hence decrease the stability of benzene rng -OCH, ° is weaker electron withdrawing group than ~COCH; one Hence ~COCH, group more stabilize the phenoxide tesco CIE sect ae ey ate pin sti ‘COOH variety of unsymmetrical ethers. The nucleophilic Aspirin substitution of halides with alkoxide leads to desired (Acetyl Salicylate) product. 29. (©) Dueto presence of methyl alcohol in liquor, Salicylic acid 20, (b) CyHsBr-+ CgHSONa 5+ CaHs - O-CaHs ‘Sod. ethoxide diethylether 30, @) CH; -CH, ~CH-CH-CH,-CH; _HlQ I 21.) OH OH CHy HNO; coos = oo o iy menptain co% a) Pai any, X DAILY PRACTICE PROBLEMS © {@) Ketones on oxidation give carboxylic acids with lesser ‘number of carbon atoms, i... cH;CocH; ©! 5cH;COOH 4€0) +H,0 © cn Sy cH Hy i « fe @ cH €~cHy cH, CH, CHO (©) Cannizzaro reaction - when an aldehyde containing no —H undergo reaction in presence of 50% KOH. It disproportionate to form a molecule of carboxylic acid and a molecule of alcohol. cro on @ oN NO, NO, Cicrie acid) Barbiturie acid) HO. O40 coon oo HO" a IL = o—c—cH, uo OH (Ascorbic acid) CAspitiny (@ ItisClemmensen’s reduction 9 a boca, -cHt, ee HCH CHSCs (©) Duetoresonance in carboxylate ion, the double bond character of C = O bond in carboxylic acids is greatly reduced as compared to that in aldehydes and ketones. CHEMISTRY SOLUTIONS DPP/CC26 on, cH,-cH, % ‘This reaction is known as Clemmensen's reduction, 10. (a) coc, CH,COOH +PC1,-+ CH LOC ase? ce Friedel Craft on gaan cbc, 2 cH, - cr, © @ ‘Since, C when heated with Br, in presence of KOH. produces ethylamine, hence it must be propanamide and hence the organic compound (A) wil be propanoic acid. The reactions follows, Cc ~cH,~coon w cH,-COONH, —*> ® cH, ~ cs ~cit ~CONH, HOH © = (CH ~CH —NH (byline) OH — HCH Cal, 10, COR 12. @ @) 2C,4,cHO (Betoin) GP_3371 DPP/ CC26 B. Ty 15. 16. W. 18. 19. 0) OH OH Phenolphthalein © coocn,, OH @ (Oil of wintergreen) () NaBH, selectively reduces the aldehyde group to alcohol without affecting double bond in a organic compound, So, X is NaBH. CcHCH=CHCHO NHL C,H, cH=CHCHLOH © cHef-0+ susewne dn 2, coon © ‘This proces is known as esterification. @) (@ Addition of HCN to carbonyl compounds is nucleophile adltion reaction, The order of eatvity of earboyl compounds is Aldehydes (smaller to higher) Ketones (smaller to higher) Then a1. © © © @ @ © a6 srl PhCOPh J 38” COONa rexoalite + Hy ° ° I i} CH, ~ C ~CH,~C- °o oO ho. I -€-Gi-C-08: (City CHCH, Be one BON, om —Bei Iydotyi CH; 9 cH, (CH3~C-CHy-CHy-CH-CH + CO, + E10H T as 8 oH I (CH; ~CH; -C-Cl —> I OcH; ° i CH ~CH ~C-OCH + HCI ‘The correct order of increasing acid strength (Me), CH.COOH < CH,COOH< MeOCH,COOH ‘< CF,COOH Electron withdrawing groups increase the acid strength and electron donating groups decrease the acid strength. Acetic acid does not have ~CHO grouping, while all others (HCOOH, HCHO and CH,CHO) have ~CHO grouping Pinacolone is oxidation product of pinaco. a oe 1868_-—<$<$ ___——_———————————- DPP/ CC26 27. (@) Aldehydes having a H stom, when treated with 29. @) I,and'Na,CO, react with acetophenone (CHsCOCH,) ‘aluminium ethoxide ( in place of NaOH or KOH), to give yellow ppt. of CHI, but benzophenone undergo Cannizzaro type of reaction with a difference (CHjCOC gH.) does not and hence can be used to that the product isolated is an ester rather than salt of distinguish between them. acid or alcohol. Such reaction in called Tischenko reaction, 1. 2cHycHo NOCH: ‘ected [cH,CooH+-cH,cH,0H]-> cH;C00C, Hs yee isan example of Claisen condensation. The product is acetoacetic ester i f q cri €-[OGaHHT]-cHt,-C-0c3His —> to ctty-C-ctt, Coch ‘cinsee) GP_3371 9. 10. u. 2 DAILY PRACTICE PROBLEMS (©) Since the organic amino compound on reaction with nitrous acid at low temperature produces an oily nitrosoamine so the organic amino compound is a secondary aliphatic amines. © @ ‘The yield in Sandmayer reaction is found to be better than Gattermann reaction, @ cucn=*$ cu, CH NH, Hono (CH-CH,—OH +N,+ H,0 © Aliphatic amines are more basic than aromatic amines. Resonance decreases the basic character due 10 elocalisation of shared pair of electrons on nitrogen within benzene nucleus. @ o localized lone pair of electron on nitrogen atom while other compounds have delocalized lone pair of electron. Nett © @ © MEN cH cH en Me (a) CHCH, cur,crcrr,ntt, 9 cr ,cH,cu,NHCOCH, * 2 @ @) CH,CH,-CH,-CH,-NH, Gi) with KOH (alcoho!) and CHC, produces bad smell @ CHC=cH Gi) gives white ppt with ammonical AgNO, @ CH,CH,CoocH, @ alkaline hydrolysis, @ CH,CHOH-CH, iv) with Lucas reagent cloudiness appears after 5 minutes 13. @) R,NNO+H,0->R,NH+HNO, 4. @ CHEMISTRY SOLUTIONS 1s, 16. W. 18. Ty a DPP/CC27 (a) Reduction of alkyl isocyanides in presence of LiAIH,, yields secondary amines containing methyl as one of the alkyl group. R-N=c+aty AS -NH-cH, Panie eg. CHy-N=C+ aH] —EAME cH, -NH-CHy ‘ey nie ‘whereas alkyl eyanides give I° amine on reduction, (@ CyHyNH; + COC; + KOH > CyHsNH.COCI+ HCI —2.CyHsNCO+HCI (©) Benzaldehyde reacts with primary aromatic amine to orm schiff base CoHSCI Benzaldetyde ++ CgHsNHy —> CgHsCH=NCgHs +H,0 HNO #504, 7 Os o: 3K No, wi ton, cl cl (@) When chlorination is done earlier than nitration, chlorobenzene formed at first step would introduce ~ NO, group in ortho-position, nt in m-position (b) Again if -NO, group is reduced earlier than the chlorination step. NH, group formed on reduction will again introduce -Cl in o-position © (@ Reduction with iron scrap and hydrochloric acid is preferred because FeCl formed gets hydrolysed to release hydrochloric acid during the reaction. Thus, ‘only a small amount of hydrochlorie acid is required to initiate the reaction @ cH.cHN c+ 0—¥ scH,ciENt, + HCOOH 1860-—__——_———______________—— DPP/ CC27 Naot 22. @) CH,CONH, —S!, cH,H, (@) CHy Te? CHSNHy 2B. a, @ © (Hofmann bromamide reaction) ‘Acetamide is basic due tothe presence of lone pair of electrons of N itis also acidic because its conjugate base shows resonance. ° ° oO ly CNH cH, CNH CH CoN (amore stable de to-ve charge on 0) Benzontie(CyH,C=N) acts as an eletrophile Lewis acid) de to electron deficiency of C of CN as well as nucleophile (Lewis base) in nature de to presence of Ione pir electrons on N hence itis neural Trethylamine and phenol are basic and acidic in nature respectively. GGuanidine is most asic because it conjugate acid is stabilized by two equivalent resonance structures, NH Nib Hy C -NH, "cH, CLNH, <> NH, NH I i * CH; C-NH, <> CH; C=NHy Further 2° amines are more basic than 1°, while amides ‘are least basic due to delocalisation of the lone pair of ‘electrons on N 0: O i) CHy-C-NH,<—>CHy- C ‘Thus the correct order of bascities is NH ots ° (CH-C -NH,_>CH,-NH > CH,CH,NH, >CHs-C-NH, (©) CHNC (methyl isocyanide) on reduction with LiAlH, gives secondary amine. (©) Only 1° amides (i.e. RCONH,) in the present case ‘undergo Hofmann bromamide reaction RCONI, +B, +4KOH —> NH +2KBe+ K,CO, +210 (afin tromamie reaetion) @ CgHlgntl, +C8 > CoHgNH cH HEC, (C6HsN =C=S+HgS +2HCI ‘Thereaction is called mustard oil reaction, ©) eon nncr.c, + C= Neer, nym win, NHCH,CH. a ° oO i} Ip _e (© R-C-c1 + NaNy > Ce x R-N=C=0+ Ny, (©) Amides are hydrolysed to give acids and NH or GP_3371 DAILY PRACTICE CHEMISTRY PROBLEMS SOLUTIONS DPP/CC28 @ 2, 4 Dinitroflurobenzene, also known as Sanger's © reagent, reacts with the HN - group of the peptide to ) from 2, 4- dinitrophenyt (DNP) derivative of the peptide. @ ‘The DNP derivative of the peptide is hydrolysed to @) give DNP derivative ofthe single amino aid 6 @ Glucow being an aldose responds Tolen's test while vicornucuconnene frocose,alheugh keto’ undergoes rexrangement Ha NCHCONHICHCONHCHCOOH + in presence of basic medium (provided by Tollen’s Ri Ro Rs reagen) to form glucose, which then responds to Tole's test 7. @ Since sucrose is dextrorotatory while hydrolysis on ae ‘Product of sucrose, having equimolar mixture of glucose and fructose, is laevorotatory. Hence the hydrolysed 0, product of sucrose is known as invert sugar andthe 2.4, no Senne Ieolsis ofsurse is known as inversion & ©) Allproteins ae not fund in L-form but they may be om oo preseatin feemotD orl FuCONG 9. (a) Butter, being lipid, dssolvesin chloroform. hook ow 10. (6) Human body can synthesize 10 of the 20 amino acids 0, ebiained by hydrolysis of varius proins {ove dea ot papi) 1. (9) Chemically amoge is a ong unbranched cain with 200-1000 a-D-(+ “glucose units held by C1-C4 Hl iycosiie nage 12. fa) 1. @ On the basis of structure of guanine and iffthe sequence of bases in one strand of DNA is I, then R, * the sequence in the second strand should be IT NO, (DNPéervativey AIT:G:C:T:T :G:A 1 H,NCHCOOH + HyNCHCOOH T:A:C:G:A:A:C:T IL b b 14. © - * : 2 ; ho cae 15, (@) Due to resonance, “CFR <> -C=NH- Zwiver on contains both +ve and ve charge. Protea C-Nbond ecquires some double bond characte, ence eet Geis eee ee ee emma ' —COO™ groupis basi sine itean accept x proton, + (€)Prolineis an acidic amino aci Glucose is considered as a typical carbohydrate which 17. (a) Isoelectric point (pH) ‘contains ~CHO and -OH group. 2@ 24. (@) DNA; double stranded o-elial structure 18. 25. © 26. Thecerret structure of thymine is 19. x7 —cH, —S it isa B-pyranose hence it is an aldohexose, a $62 -_-<$ —@$ —_§_—_—_—_—__________ DPP/ CC28 27. (b) The DNA sequence that codes for a specific protein is, called a Gene and thas every protein ina cell has a 30. (@) CHO Crewe corresponding gene. snansit, | ss NnIPh + Pantie 28, @ Enzymes are very specific biological catalysts CHOW: CHEN.NHPh + PLNH;+ NH possessing well-defined active sites (cHom, (cHoH, 29. (b) In DNA and RNA heterocyclic base and phosphate ester are at Cy! and C, respectively ofthe sugar by.on buon molecule, GP_3371 u. 2 DAILY PRACTICE PROBLEMS © @ © © @ @ © 2@ 3@ “Molecules of a polymer, being largein size, seater light Polythene isa linear polymer "Nylon-6 can be manufactured from Q OC NH,OH “a, 0 Z NOH con t90, , S, reamangenen) ©: wenem) H eapricnm nol INH (CHp);- Cf ~RRHHING fr cHy)5- coo™} honiteis ahard highly vulcanized rubber, containing 20-30%, rubber Formula of the monomer indicated in bracket, (CH,),C-CH,, corresponds to2-methylpropene 10. ©) [Neoprene is a polymer of chloroprene. Hence, correct representation is a 1 0 or proses nCH, =CH—C =CH, Cloroprene I a Neo Biodegradable polymer is Nylon-2- Nslon which is copolymer of lycine H,N-CH,~COOH) and amino caproic acid (H,N-(CH,),~COOH) nH1,N- CH, ~COOH + nHyN ~(CH,),-COOH Chae | nia fia ~C =CH-CHy~ i i €HIN— CH, ~C-HN-(CH))5-C nylon -2—nylon—6 CHEMISTRY SOLUTIONS 13. 18. wo DPP/CC29 () High density polythene is formed when addition polymerisation of ethene takes place in a hydrocarbon solvent in presence of catalyst such as ziegler-Natta catalyst. o (©) CH; = C-CH= CH, (chloroprene) is the monomer of neoprene. a CH = CH, Pageet =CH-CH}, (©) Buna— Nisa copolymer of butadiene (CH,=CH-CH=CH,) and acrylonitrile (CH, =CHCN), (@) Nylon 6, 6 has amide linkage capable of forming, hyirogen bonding, (@ Theconcemned chemical reactions are (@ CaCy+2H,0 > Ca(OH), + CoH CH, +H, > Cay Byler 288g i iyo, ey ries Ts tiga a6 ge 26 yen wishin gives 28 kg of ethylene whose 28 kg gives 28 kg of the polymer, polythene, © (©) nHOOC(CH,),COOH+ nHN(CH)gNHy e ¢ i i [-C-(CH,-C-NHAcH) Nylon 5.6 ask, Poymerison 21.(@) Nylon-66 is « polyamide, hence it has only CONH- linkage and no -COO- linkage NH, © © © @ @ @ Orlon is a tradename of polyacrylonitrle Melamine plastic erockery is a copolymer of HCHO and Melamine . ) (@ Nylon and cellulose, both have intermolecular hydrogen bonding, polyvinyl chloride has dipole- ‘dipole interactions, while natural rubber has van der Waal forces which are weakest Neoprene is a polymer of chloroprene (2 chloro ~ 1,3 — butadiene). @ @ DAILY PRACTICE PROBLEMS 1. @) Given drugisused as anaci 2 © 3 @ 4 © 5s @) & @) Ieis acetyl slice acd i. aspirin, analgesic and apart, 1. @ Whiteware possesses good strength, translucency, and low porosity & ©) 9. (Glyceryl dinitrate not usedas fixative inpefumes, 1. &) 1. @_ Drugs that mimic the natural messenger by switching on te receptor ar aledagoniss. While dogs that finds tothe ceptor site and inhibi natural fanction arecalledanagons 12. @) The mixture of chloroxylenol and terpenol is dettol vihich is used as antiseptic 13, (© We know that N-acetyl para-aminophenol (or paraceamod isan antiptee which can sso be used sam analgesictoreleve pain 4 @ 15, (@) Benzalkonium chloride, also known as alkyldimethylbenzylammonium chloride snitrogenous cationic surface active agent belonging to the quaternary ammonium group. Ibis used as antiseptic. 10,12, 14,1618 16. W. 18. oH CHEMISTRY SOLUTIONS @ @ @ © © @) DPP/CC30 Bacteriostatic drugs inhibit the growth of organism, ‘while bactericidal drugs kill the microorganisms. Narrow spectrum antibiotics are effective against Gram-positive or Gram-negative bacteria. Limited spectrum antibiotics are effective against a single ‘organism or disease. Linear alkylbenzenesulphonates (LAB) carrying phenyl chains at secondary positions are biodegradable ‘Theterm “antihistamine” refers only toH, antagonists, Which is also known as Hy-receptor antagonists and H,-antihistamine. Magnesium hydrosilicate forms base of Taleum powder. tis the known structure of Penicillin G Aluminium salts present in deodorants act as antibacterial agents Pheromones are the chemical substances used by insects for communication, Dilute solutions of boric acid and hydrogen peroxide are weak antiseptics Sucrose is natural sweetner, Broad spectrum antibiotics act on different antigens. GP_3371 Mock Test Full Syllabus Chemistry L Let v,bethe frequency ofthe series limit ofthe Lyman series, vbe the frequency ofthe frst lineof the Lyman series, and v, bethe frequency ofthe series limit ofthe Balmer series then— w 4 @7 When an isolated gaseous cation X°(g) is converted into © 5 X(g) anion, the amount of energy released is 16.8eV. Caleulate the electronegativity value of the atom X on Pauling’s scale, @ 1 2 o4 @3 Unknown sample (A) on heating swells up first and aqueous, solution of (A) gives white pp. with NaOH which becomes. soluble with excess of NaOH addition — @) Borax (6) Alum (©) Microcosmicsalt _() None AL6TSK, Hy(@) and CO (a) reac to form CO(B) and H,0 (8), K, forthe reactions 0.16. Ifa mixture of 0.25 mole of H,(g) and 0.25 mol of CO, isheated at 675K, mole % of CO(8) in equilibcium mixture is— @ 14 () 1428 © 237 @ 33 Choose the correct option for ‘Anhydrous HI Cone, yy HI 1 | (@) Land are identical (©) Land Mare different (©) Mechanism of formation off and Il arenot known. (@ None ofthese 2 4 For the extraction of Pb when impurity contents veryhigh, then during roasting of galena, the formation of which ‘compound (s) is/are prevented by lime — (@) PSO, (6) PDsio, (©) Both(a)and(b) —(@)_CaSiO, Polymer obtained by rection of phenol and formaldehyde is (@) Bakelite ()Terytene (©) Nylon-66 (©) Urea formaldehyde resin ‘The conductivity of a saturated solution of Ag,PO, is 9 10-6 Sm and its equivalent conductivity is 1.50% 10-4 Sin? equivalent"). The Ky, of g;PO, is— @ 432«10 () 18*109 (© 86410 (@ None of these Which statement is incorrect regarding thermite process — (@)_ 3partmetal oxide +1 part Alistakenas thermite mixture (©) Ignition mixture (Mg powder + BaO,) acts as catalyst (©) Metals (Fe, Cr) are obtained in vapour form (@, Reaction is exothermic due to highly +ve enthalpy of formation of Al,0; Which ofthe following option is having maximum number ‘of unpaired electrons — (@) A tetrahedral dion (©) (CofH,0).* (©) Asquare planar dion (@ co-ordination compound with magnetic moment of 52BM, pH ofa saturated solution of silver salt of monobasic acid HA is found to be 9. Find the K,, of sparingly soluble salt ABA(S).Given K, (HA) = 10-" @ 1x10 (©) bo” © Lixo! @ we Which of the following carbide does not release any hydrocarbon on reaction with water. © ©) BEC © ca, © MgC, Phenol and benzoic acid i separated by ~ (@) Natico, © Neon © N (@ Navn, 2 Mock Test Full Syllabus Chemistry 15, For the rection takes place at certain temperature NH,HS —_(@) Statement is alse, Statement-2s true. = NE (g) + H,S (),ifequilibrium pressureisX bar then (Statement i true, statement-2 istrue and statement. ‘AG? would be— 2s correct explanation for statement-1 @) -2RTInx 0) -RTIngx—In2) (©) ‘Statement: is true.statement2is true and statement-2 (©) -2RT(InX-In2) — (d)_None of these isNOT correet explanation for statement-1 16 Aqueous solution of (M) + (NH,),S -> yellow ppt (B) (4). Statement- is true, Statement-2is false. (0810282 insoluble, Te variation of concentration of A with time in two experiments starting with two different initial concentration ‘The cation presen in (M) is~ of A is given in the following graph. The reaction is @ cas () sns, represented as A (aq)-» B (aq). Whats therate of eaetion © ce (sn (Mimi) when concentration of Ain aqueous solution was 17, How many pairs of enantiomers ate possible for following «18M. ‘complex compound. [M (AB) (CD) eff : (where AB, CD-Linsymmetrcal bidentate igand, te f-Monodntat ligands) tis @ » ws e™ © 0 @ 8 £ 12. 18 For the reaction A(g) +2B (g) = C(g)+ D(g); Ke=10 a Ifthe inital moles ofA, B, Cand D are 05, 1, 0.5 and3.5 Zoos moles respectively in a one litre vessel. What is the © og Experiment ‘equilibrium concentration of B? o7 {experitnent-2 @ 10+ () 2104 ne 3 fo 15 0 eos teen tio (ni, —> 19, H,Szasisnotevolved when SO,?ionreacts with following _-@)_0072Mmin © 036M mir! reagents (© 01296Mmin! Min? (@) Zr+diL 180, (b) AL+Cone. NaOH NH,C10, + HINO, (dilute) > X-+HCIO, (© Altai HCl (8) None ofthese x5 (g15) 2 Me-CH=CH,+CHCI, —"°H 5 (Major prods is— Gas(¥)is~ as @ © ON, 9 © No, @ NO KX OK 24. Choose the core order ofT (True) and F(Flse)— @ ‘OK (0) Y (1) When the pH of rain water is below 3.6, itis called acid @) Ozone hole occurs aver Antarctica mainly during September-October and it gets replenished in © A @ Aen November-December, 7 ou @)_ Methyleyclohexane isan ozone-depleting molecule. 21, Thisquestion contains Statement-1 andStatement2.Ofthe (4) CODis always larger than BOD. four choices given after the statements, choose the one that, best deseribes the two statements, Statement 1: [Hell}*is more stable as compared toH," ‘Statement 2: Both the above species ae having equal bond order. (@) TTTF ©) FF () FIFT (@ rrr GP_3371 Mock Test Full Syllabus Chemistry End product (B) of above reaction is— aaa Ow Oherr ° Ore” Er <— Qh anon Ql cose © @ CG ‘CH,OH © cope Precautions tobe taken in the study of reaction rae forthe reaction between potassium iodate (KIO,) and sodium salphite (Na,SO,) using starch solution as indicator at different concentrations and temperature ~ (@) The concentration of sodium thiosulphate solution should always be less than the concentration of the potassium iodide solution, (b)_ Freshly prepared starch solution should be used (© Experiments should be performed with the fresh solutions of H,O, and KI, @ Allo these Calculate the millimoles of 0 following data in solution on the basis of M TOiml of {solution of BIO, was added toe? solution, ‘Thebromine evolved was removed by boiling and excess of | 0nd death 2S an of NaAsO, ‘The reactions are given below. () 00% m0; +11" + Se0F +5 +150 (@) BrOs + A805 +1140 Br + ASOP +* (a) 16* 10% (&) 125 © 25 (@ None of these | mole of gas X is present ina closed adiabatic vessel ited with a movable etonlss piston, The initial temperature of| ‘228 X is 300 K. The vessel ismaintained at constant pressure ‘of atm. Keeping the pressure constant at Iatm the reaction GX (g)—>2Y(g) ; AH=-30 kdmol started with thehelpof| negligible amount of electric energy. If finally 25 mole % of X undergone reaction at constant pressure of aim, find the final temperature (in K) of reaction vessl. Given :C, go "400K mole, Cag) 30K mole. @ 6oK © 30K © 120K (@ 100K In the given molecule choose the corret order oftheir angle. Be wo So-H (@) x>y>z () xz (@)Can'tbe predicted ‘What would be the reduction potential of an electrode at 298K, which originally contained IM K,Cr,0, solution in acidic buffer solution of pH = 1.0 and which was treated with 50% ofthe Sn necessary to reduce all Cr,0,2-toCr™, ‘Assume pH of solution remains constant. Given: 2.303RT F (@) 1285V ©) 1193V © Ls (@ None of these Mock Test Full Syllabus Chemistry —— ® Soiutions #8) @ — eat X. me mm Shaving carbanion characters Hofinann alkenes major product. (@X*(@)—>X"(g) sEnergy=IE+1A= 168eV IA+EA _168 my 56 56 puting (©) K,S0, Al (604), 280-—*-9K,0, + Al (S04), +2480 oe aren pd K,S0, 904) 24,0 AN4OH —»2KOI+2A4OID | 48,80, vehi Wey) see Exe of NOt (AMO). soluble ©) H,(g)+CO,(g) = CO(g) + H,0 (8) At eg™ 0.25-x 0.25-« x x =0.16= —*— 5 04= Kyo 016> Gara eae x= 071d 301-04x=x ons Moet of CO (g)= 22TH 100 = 1428 CO) anhydrous a »o sc /o Ho Cone. HI Sx 19 ou (©). Byintermittenty filled lime theblown ar in the sinterer ‘gels diffused and PbS particles come under limited supply of ar therefore formation of PSO, i prevented 3 PoS+ 5 0+ Pb0+S0; POO + Si0, -> PDSIO, gangue PDSiO,+CaO > CaSiO, + POO more basic less basic on ® +HCHO PSH okelte = x 1000 =n te 1000 1.50% 10-4 104=9 10-6 102 N=6 x10 s=M=N 88107 29 10° mol/L ‘AgsPO,= 3Ag*+PO, ass k= GS).S=278!=27% (2% 105) 24.32% 10-18 (@) (Mg powder + BAO; atsas ignition mixture Fe, Crare obained in molten state Enthalpy of formation of Al,O; is negative. GP_3371 Mock Test Full Syllabus Chemistry n B. 4. @ @ roceranoaasion, [1] 1111111 4 unpaired electrons © Foricotto, = [LL] 1 O unpaired electrons (©) Forsquare planara?ion, {1h | 1L | 1] 1 1 unpaired electrons @) BM.= Jnin+2), S92BM.= Jala2) ‘n= 5 unpaired electrons (©) Ag(l) = Ag*(aq)+A-(ea) = unpaired electrons x x-y Ag(1) +10 (0 HA (aq) + OFF (aq) xy y y io _ aos K- KGW 1 &y) x-y=106 x= 1054106 xeLldo$ Kyo 11x 10-5 x 10% Kahl 10 (2) (@)SiC= Covalent carbide (6) Be,C+ 41,0 —» 2B0(08), + CH? (0)CaC, +21,0 —> HC=CHT+CaOHD, (@)Mg,C, +2H,0 —> 2Mg(OH), +HjC-C=CHT (@) PhOH+NaHCO, —> Noreaction PhCOOH + NalICO, —+ PhCOBN:® +H,0+-C0, ‘ealt) © =-2RT(InX~In2) (oa) GdS 1 +(NH),S—> cads.4 4S, Cast Yelow tne (8) sas, J Nt), —>, Sas 4 ENE, 9505, ‘Yew Sou (6) C8" + (uttaysS—+ cas} O82 Cs ‘Yellow inslabe (@) So +414 ,S—> $05 1 On ‘acum sles Kd B® — A@®)+2B@) = C@+DO Ateg® OS-x 1-2x OStx 354 ~y xy sl x4 (due to very high value of equilibrium constant) rot bet yxQy + y= 10-4; [B(@))=2y>2* 10-4 © So} +2a1+201- +31,0—95* + 2(AK01,F 1H, does not evolve as liberated His neutralized by NaOH and Na, Sis formed. 2% ) 00% Me-citcry cic OM, cud ae fee en, " Say ql on Fon vs ¥ & cGy EOS cH, cha, Eo ok, 21. (@)_ [HeH}*, M0. configuration ots? BO=10 6 Mock Test Full Syllabus Chemistry Hy*, MO. configuration ols! (0) Freshly prepared starch solution should be used B.O.=05 (©) Experiments should be performed with the fresh Higher the B.O. mor isthe stabil. solutions of #09 and KI 2 (@ Ratelaw r=K{Al™ “4 2. (©) (a) SeOF + BIO5 +H" 8603+ By +10 11 =(22) Min fom gph (exp 1 oe os (0) Bios +A%5 41,093 + ASP 4H 15 =(22) m/min fom graph (2.2) apap 5 fo, of BO, = gm 09. of S07 1251 sagt ogg, 22 BS hereto oe 05 “6 7 In reaction (1) kx (A]> x18 =0072Mai! tes of BrO consumed ZB. ()_NU,CIO, + HNO, ae)» NINO, +HC10, ~ meq. of Se0,2 heat «2=107 x: NINO, te, Nj0+214,0 sof A2=107 5 no memes muidertesineneg # MabetXraset07S ok oo wanin ofrainwaterisbelows 6, Hise ‘Heat liberated at constant pressure = 0.75 * 10 kJ ©) Ozone hole occurs over Antarctica mainly during MoleotXremsining= mole September-October and it gts replenished in November-Docemba ©) Methyleycloberane is not an ozone-depleting mle, (4) BOD Giological oxygen demand) isa measure of (} organic pollutant present in the sample of wate. 4 ‘Higher is the value of BOD, higher is the level of 7500 ceganic potion in wate. Te aroun of oxygen r= 73%, = 300 (int consumed fr oxidising al organic and 03 oxidise ing materialin a sample of water isclld chemical oxygen demand (COD) Final temperature=300-+300= 600K COD isalways ager than BOD. Och i B® ° SQ — RX acon eo wR Pe aon (more stable structure) (less stable structure) tence les contribution 9 oO Therefore, repulsion between bth C—O bonds willbe 26 @ (@ The concentration of sodium thiosulphate solution should always be less than the concentration of the potassium iodide solution. greater than the repulsion between C —H bond and (C— OH bond or betwoen C-Hand bond. GP_3371 Mock Test Full Syllabus Chemistry Repulsion between C - Hand C = O bond is greater than that ofbetween C- H and C- OH bond, because Egy = Bp 22 og OEE

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