Set 4 3 Chemistry Board
Set 4 3 Chemistry Board
SECTION A
Questions no. 1 to 18 are Multiple Choice (MCQ) type Questions, carrying
1 mark each. 18 1=18
1. A compound CaCl2 . 6H2O undergoes complete dissociation in water. The
(a) 9 (b) 6
(c) 3 (d) 4
2. For a zero order reaction of the type A products, the rate equation
may be expressed as :
A0 A A A0
(a) k (b) k
t t
A0 A A0 A .t
(c) k (d) k
2t 2
2+
3. Which of the following Cu halide is not known ?
(a) CuBr2 (b) CuI2
(c) CuCl2 (d) CuF2
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4. Which of the following structures represents -D-glucose ?
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8. Reaction of 1-phenyl-2-chloropropane with alcoholic KOH gives mainly :
(a) 1-phenylpropene (b) 3-phenylpropene
(c) 1-phenylpropan-3-ol (d) 1-phenylypropan-2-ol
9. Corrosion of iron is :
(a) a decomposition process
(b) a photochemical process
(c) an electrochemical process
(d) a reduction process
10. The number of molecules that react with each other in an elementary
reaction is a measure of the :
(a) activation energy of the reaction
(b) order of the reaction
(c) stoichiometry of the reaction
(d) molecularity of the reaction
13.
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14. The crystal field splitting energy in tetrahedral crystal field ( t) is equal to :
4 9
(a) o (b) o
9 4
4
(c) o (d) 2 o
3
For Questions number 15 to 18, two statements are given one labelled as
Assertion (A) and the other labelled as Reason (R). Select the correct
answer to these questions from the codes (a), (b), (c) and (d) as given below.
(a) Both Assertion (A) and Reason (R) are true and Reason (R) is the
correct explanation of the Assertion (A).
(b) Both Assertion (A) and Reason (R) are true, but Reason (R) is not
the correct explanation of the Assertion (A).
(c) Assertion (A) is true, but Reason (R) is false.
(d) Assertion (A) is false, but Reason (R) is true.
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SECTION B
(b) [Ni(NH3)6]Cl2
1
20. Name the cell which : 4 =2
2
(a) was used in Apollo Space programme.
(b) is used in automobiles and inverters.
(c) is suitable for hearing aids and watches.
(d) does not give a steady potential and is used in transistors.
OR
(b) Define Azeotrope. What type of azeotrope is formed by negative
2
Conc. NaOH
(i)
H
(ii) + H2NNH CO NH2
OR
(b) Do the following conversions in not more than two steps : 2 1=2
(i) Toluene to Benzoic acid
(ii) Benzaldehyde to 1-Phenylethanol
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23. The rate constant for the first order decomposition of N2O5 is given by
the following equation :
2 104 K
log k = 23 6
T
Calculate Ea for this reaction. 2
1 1
[R = 8 314 J K mol ]
SECTION C
27. The following data were obtained during the first order thermal
decomposition of C2H5Cl at a constant volume :
C2H5Cl (g) C2H4 (g) + HCl (g)
Experiment Time (s )
1 Total pressure
(atm)
1 0 04
2 100 06
Calculate the rate constant. 3
(Given : log 2 = 0 3010, log 3 = 0 4771, log 4 = 0 6021)
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1
28. If benzoic acid (M = 122 g mol ) is associated into a dimer when
dissolved in benzene and the osmotic pressure of a solution of 6 1 g of
benzoic acid in 100 mL benzene is 6 5 atm at 27 C, then what is the
percentage association of benzoic acid ? 3
1 1
(Given : R = 0 0821 L atm K mol )
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SECTION D
The following questions are case-based questions. Read the case carefully and
answer the questions that follow.
OR
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32. Amines are usually formed from nitro compounds, halides, amides,
imides, etc. They exhibit hydrogen bonding which influences their
physical properties. In alkyl amines, a combination of electron releasing,
steric and hydrogen bonding factors influence the stability of the
substituted ammonium cations in protic polar solvents and thus affect
the basic nature of amines. In aromatic amines, electron releasing and
withdrawing groups, respectively increase and decrease their basic
character. Influence of the number of hydrogen atoms at nitrogen atom
on the type of reactions and nature of products is responsible for
identification and distinction between primary, secondary and tertiary
amines. Presence of amino group in aromatic ring enhances reactivity of
the aromatic amines. Aryl diazonium salts provide advantageous
methods for producing aryl halides, cyanides, phenols and arenes by
reductive removal of the diazo group.
Answer the following questions :
(i) Arrange the following in the increasing order of their pKb values in
aqueous solution : 1
C2H5NH2 , (C2H5)2NH, (C2H5)3N
(1)
(2)
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SECTION E
(ii) Write the ionic equations for the oxidizing action of MnO 4 in
acidic medium with
(1) I ion, and
(2) Fe2+ ion. 3+2=5
OR
(b) (i) Name two oxometal anions of the 3d series of the transition
metals in which the metal exhibits the oxidation state equal
to its group number.
(ii) What is the effect of increasing pH on a solution of K2Cr2O7 ?
(c)
(d) Why are -hydrogen atoms of aldehydes and ketones acidic in
nature ?
(e) Write a chemical test to distinguish between Benzaldehyde and
Benzoic acid. 5 1=5
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35. (a) (i) Calculate the emf of the following cell at 298 K :
3+ 2+
Al (s) Al (0 001 M) Ni (0 1 M) Ni (s)
[Given : E 3 = 1 66 V, E = 0 25 V, log 10 = 1]
Al / Al Ni2 / Ni
OR
+
(b) (i) The molar conductivities of NH 4 and Cl ion are
1 1
73 8 S cm2 mol and 76 2 S cm2 mol respectively. The
2
conductivity of 0 1 M NH4Cl is 1 29 10 S cm 1. Calculate
its molar conductivity and degree of dissociation.
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MARKING SCHEME
Senior Secondary School Examination, 2023
CHEMISTRY (Subject Code–043)
[ Paper Code: 56/4/3]
Q. No. EXPECTED ANSWER / VALUE POINTS Marks
SECTION-A
1. (c) 1
2. (a) 1
3. (b) 1
4. (a) 1
5. (d) 1
6. (b) 1
7. (a) 1
8. (a) 1
9. (c) 1
10. (d) 1
11. (b) 1
12. (b) 1
13. (c) 1
14. (a) 1
15. (c) 1
16. (a) 1
17. (b) 1
18. (a) 1
SECTION-B
19. (a) aquacyanidobis(ethane-1,2-diamine)cobalt(III) ion 1
(b) hexaamminenickel(II) chloride 1
20. (a) Fuel cell
(b) Lead storage ½x4
(c) Mercury cell
(d) Dry cell
21. (a)
1
• Positive deviation,
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• On adding acetone, some of the hydrogen bonds of ethanol are broken down
causing an increase in vapour pressure / the ethanol-acetone shows weaker
interactions than pure ethanol-ethanol and acetone-acetone interactions. 1
OR
(b)
A liquid binary mixture that distills at constant temperature without undergoing a
1
change in composition.
Maximum boiling azeotrope ½
68% HNO3+ 32% H2O ½
22. (a)
(i)
(ii)
OR
(b) (i)
(ii)
(or any other correct method of conversion in not more than two steps)
23. Ea
log k = log A –
2·303 RT ½
Ea
– = – 2 104 K ½
2·303 R
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½
25. ½
SECTION-C
26. (a) Due to the resonance stabilisation of benzyl carbocation. 1
(b) Because it is a racemic mixture / it contains an equimolar mixture of the two
enantiomers of butan-2-ol. 1
(c) Because it forms a poisonous gas phosgene in presence of air and light. 1
27. ½
1
(Deduct ½ mark for no or incorrect unit)
28. n
= i B RT
V ½
W 1000
6·5 = i x B 0·0821
MB V
1
6·1 1000
6·5 = i x x 0·0821 300 K
122 100 L
6·5 122
i= = 0·528 ½
6·1 0·0821 300 10
1– i 1 – 0·528
= = 1 = 0·944 or 94·4%
1 1– 1
1– 2
n
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29. (a) (i)
(ii)
(2)
1
(ii) Because NaOCH3 acts as a strong base which leads to elimination reactions. 1
6 2
30. (a) Fe = 3d 4s
3d 4s 4p
Fe3+ =
Fe3+ =
in presence of CN–
[Fe[CN6]3– =
6 CN–
Hence hybridization is d2sp3
(b)
(c) Cl– being a weak field ligand does not cause pairing of electrons and hence
[NiCl4]2- is paramagnetic while CO being a strong field ligand causes pairing of
electrons therefore [Ni(CO)4] is diamagnetic.
(d) Linkage isomerism. Example, CN – / 𝑵𝑶– / SCN –
𝟐 1x3
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SECTION-D
31. (i) Peptide linkage : A linkage formed when two amino acids are joined through 1
– CONH – bond.
Glycosidic linkage: When two monosaccharides are joined through oxygen atom.
(or any other correct difference)
(ii) Those which are not synthesised in the body and must be obtained through diet. 1
(iii) -helix and -pleated sheet.
1
Hydrogen bond, van der Waals forces, disulphide linkages, electrostatic force of
attraction. (any two) ½,½
OR
(iii) Loss of biological activity when native form of protein is subjected to change in 1
temperature, pH, etc. Example, curdling of milk (or any other suitable example)
Secondary and tertiary structure lose their biological activity. 1
32. (i) (C2H5)2NH < (C2H5)3N < C2H5NH2 1
(ii) Due to the protonation of aniline to form anilinium ion which makes it
deactivating and meta-directing. 1
(iii)
1
½
OR
(1)
(2)
1x2
SECTION-E
33. (a) (i)
(1) Because of no unpaired electron in d-orbitals in Zn2+ whereas, Ni2+ has 2 1
unpaired electrons in d-orbitals / Ni2+ shows d-d transition while Zn2+ does not.
(2) Because Cr is more stable in + 3 oxidation state due to stable t2g3 configuration. 1
(3) Because of their ability to show multiple or variable oxidation states / ability to
1
form complex / provide larger surface area for the reactants.
(ii)
(1) 𝟐 𝑴𝒏𝑶– + 10 I – + 16 H+ ⎯⎯→ 2 Mn2+ + 5 I2 + 8 H2O
𝟒
1
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OR
(b)
(i) Dichromate ion/ Chromate ion / Permanganate ion (any two)
2–
(ii) Changes to CrO 4 / K2CrO4
(iii) Cu+ ion (aq.) undergoes disproportionation to Cu2+ (aq.) and Cu /
2 Cu+ (aq.) ⎯⎯→ Cu2+ (aq.) + Cu
(iv) Cerium /Terbium
(v) Chromium, Copper 1x5
34. (a)
1
(b)
(c)
1
(Deduct ½ mark for no or incorrect unit)
(b) (i)
(ii) As seen from the curve, it runs parallel to the y-axis. So, even on extrapolation,
it will not intercept, hence 𝛬°𝑚 cannot be obtained. 1
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