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ISC Class 12 Chemistry Question Paper Solution 2018

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ISC Class 12 Chemistry Question Paper Solution 2018

Uploaded by

upadhyayyuvraj68
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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ISC Class 12 Chemistry Question Paper

Solution 2018

CHEMISTRY THEORY (PAPER 1)

Question 1
(a) Fill in the blanks by choosing the appropriate word/words from those given in the [4×1]
brackets:
(square pyramidal, electrical, 74, 26, sp3d2, sp3d, chemical, 68, 32, tetrahedral, yellow,
white, iodoform, Lucas)
(i) A Galvanic cell converts _______ energy into ______ energy.
(ii) The percentage of unoccupied spaces in bcc and fcc arrangements are _______
and ________ respectively.
(iii) Propan-2-ol on reaction with iodine and sodium hydroxide gives ______
precipitate and the reaction is called ________test.
(iv) The geometry of XeOF 4 molecule is ________ and the hybridisation of xenon
atom in the molecule is __________.

(b) Complete the following statements by selecting the correct alternative from the [4×1]
choices given:
(i) During the course of an S N 1 reaction, the intermediate species formed is:
(1) a carbocation
(2) a free radical
(3) a carbanion
(4) an intermediate complex
(ii) Purification of aluminium by electrolytic refining is called:
(1) Serpeck’s process
(2) Hoope’s process
(3) Hall’s process
(4) Baeyer’s process
(iii) An aqueous solution of urea freezes at −0·186oC, K f for
water = 1·86 K kg mol-1, K b for water = 0·512 K kg mol-1. The boiling point of
urea solution will be:
(1) 373·065 K
(2) 373·186 K

10
(3) 373·512 K
(4) 373·0512 K
(iv) In the dehydration of alcohols to alkenes by heating with concentrated sulphuric
acid, the initiation step is:
(1) formation of carbocation
(2) formation of an ester
(3) protonation of alcohol molecule
(4) elimination of water
(c) Match the following: [4×1]
(i) Rate constant (a) Dialysis
(ii) Biodegradable polymer (b) Glycine
(iii) Zwitter ion (c) Arrhenius equation
(iv) Purification of colloids (d) PHBV
(d) Answer the following questions:
(i) (1) Why does the density of transition elements increase from Titanium to [4×2]
Copper? (at. no. Ti = 22, Cu = 29)
(2) Why is zinc not regarded as a transition element?
(at. no. Zn = 30)
(ii) Identify the compounds A, B, C and D.
𝐻𝐻2 𝑂𝑂/𝐻𝐻 + 𝑁𝑁𝐻𝐻3 ℎ𝑒𝑒𝑒𝑒𝑒𝑒 𝐵𝐵𝑟𝑟2 /𝐾𝐾𝑂𝑂𝐻𝐻
𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶 𝐴𝐴 𝐵𝐵 𝐶𝐶 𝐷𝐷

(iii) Calculate the osmotic pressure of a solution prepared by dissolving 0·025g of


K 2 SO 4 in 2·0 litres of water at 25oC assuming that K 2 SO 4 is completely
dissociated. (mol. wt. of K 2 SO 4 = 174 g mol-1)

(iv) What type of isomerism is shown by the following coordination compounds:


[Pt Cl 2 (NH 3 ) 4 )] Br 2 and [Pt Br 2 (NH 3 ) 4 ] Cl 2 .
Write their IUPAC names.

11
Comments of Examiners
(a) (i) Some candidates filled electrical and chemical in Suggestions for teachers
the blank instead of chemical and electrical. − Explain electrochemical cell and its
(ii) Many candidates wrote 68% and 74% instead of working thoroughly.
32% and 26%. − Discuss different types of unit cells
(iii) A few candidates wrote white precipitate instead and their packing in detail.
of yellow precipitate and Lucas test instead of − Give adequate practice for different
tests based on organic reactions.
iodoform test.
− Explain the geometry and
(iv) Some candidates wrote tetrahedral instead of hybridization of compounds with
square pyramidal in the first blank while a few examples.
candidates wrote d2sp3 instead of sp3d2 in the − Explain the mechanism of organic
reactions in a stepwise manner.
second blank.
− Ask the students to learn colligative
(b) (i) Some of the candidates wrote carbonation instead properties in detail.
of a carbocation. − Interpret topics such as biodegradable,
(ii) Instead of Hoope’s process, some candidates polymers, biomolecules, surface
gave incorrect options such as Baeyer’s process chemistry and chemical kinetics in
or Hall's process. detail.
(iii) Instead of 373.0512 K a few candidates wrote − Ask students to learn periodic
373.512 K or 373.065 K which was not correct. properties of transition elements.
(iv) Many candidates wrote the formation of − Give more practice in conversion of
organic compounds. Every step of the
carbocation or elimination of water instead of
conversion must be shown with proper
protonation of alcohol molecule. conditions.
(c) Most of the candidates gave correct answers. In a few − Point out the importance of Van’t Hoff
cases, purification of colloids was matched with factor while teaching abnormal
glycine and zwitterion with dialysis. molecular weight.
− Clarify isomers and isomerism of
(d) (i) (1) Most of the candidate did not write the correct coordination compounds with
explanation for increase of the density of examples.
transition elements. Their explanation was in − Explain rules of nomenclature with
emphasis on correct spelling.
terms of increase in atomic number instead of
increase in nuclear change.
(2) The reason for zinc not being regarded as a
transition element was not written properly by
majority of the candidates.
(ii) Most of the candidates identified compounds A, B, C and D correctly but some candidates failed
to identify B as CH 3 COONH 4.
(iii) The value of osmotic pressure was not calculated correctly by most of the candidates. Van’t Hoff
factor was not considered, hence the answer obtained was one-third of the correct answer.
(iv) The type of isomerism was correctly identified by most candidates, but many could not write the
correct nomenclature of the compounds.

12
MARKING SCHEME
Question 1
(a)
(i) Chemical, electrical
(ii) 32, 26
(iii) Yellow, iodoform
(iv) Square pyramidal, sp3d2
(b)
(i) 1 or a carbocation
(ii) 2 or Hoope’s process
(iii) 4 or 373·0512 K
(iv) 3 or Protonation of alcohol molecule
(c)
(i) Rate constant (c) Arrhenius equation
(ii) Biodegradable polymer (d) PHBV
(iii) Zwitter ion (b) Glycine
(iv) Purification of colloids (a) Dialysis
(d)
(i) (1) On moving from Ti to Cu, the atomic radii decrease due to increase in nuclear
charge. Therefore, atomic volume decreases with increase in atomic mass.
Hence, density increases.
(2) Zn has completely filled d-orbitals in its atomic as well as in its common
oxidation state. (Zn+2) OR d10 configuration.
𝐻𝐻3 𝑂𝑂 + 𝑁𝑁𝐻𝐻3 ℎ𝑒𝑒𝑒𝑒𝑒𝑒
(ii) 𝐶𝐶𝐶𝐶3 − 𝐶𝐶 ≡ 𝐶𝐶 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶4 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶2

[A] [B] 𝐵𝐵𝑜𝑜2 + 𝐾𝐾𝐶𝐶𝐶𝐶 [C]


or 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶2
[D]
[A] 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶/ Acetic Acid
[B] 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶4 / Ammonium Acetate
[C] 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶2 / Acetamide / Ethanamide
[D] 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶2 / Methyl Amine
𝑛𝑛 𝑤𝑤
(iii) 𝜋𝜋 = 𝑖𝑖 𝐶𝐶𝐶𝐶𝐶𝐶 𝑜𝑜𝑜𝑜 𝑖𝑖 𝐶𝐶𝐶𝐶 𝑜𝑜𝑜𝑜 𝑖𝑖 𝐶𝐶𝐶𝐶
𝑉𝑉 𝑚𝑚𝑉𝑉
3×0·025
= 174×2
× 0 · 0821 × 298

= 5·2728 ×10-3atm

13
(iv) Isomerism - Ionisation Isomerism
IUPAC names - tetraamminedichloridoplatinum(IV) bromide and
tetraamminedibromidoplatinum(IV) chloride

[2]
Question 2
(a) (i) Write the rate law expression for the reaction A + B + C → D + E, if the order of
reaction is first, second and zero with respect to A, B and C, respectively.
(ii) How many times the rate of reaction will increase if the concentration of A, B and
C are doubled in the equation given in (i) above?
OR
(b) The rate of reaction becomes four times when the temperature changes from 293 K to
313 K. Calculate the energy of activation (E a ) of the reaction assuming that it does not
change with temperature. (R = 8·314 J K-1 mol-1)

Comments of Examiners
(a) (i) Rate Law expression for the reaction A+ B+ C
D+E was answered correctly by many candidates. Suggestions for teachers
However, some candidates gave the expression as: − Explain the Rate Law expression with
rate = [A]1[B]2[C]° or rate ∝ K[A]1[B]2[C]°, examples. Also give adequate practise
which was incorrect. for different order reactions.
(ii) The increase in the rate of reaction was calculated − Make the relationship between change
correctly by most of the candidates. in concentration and rate of reaction for
(b) Some candidates used incorrect formula while a different order reactions clear to the
students.
few others wrote wrong value of ‘R’. Instead of
− Teach how Arrhenius equation is used
writing R= 8.314 J K-1 mol-1 they wrote R=0.0821.
to calculate the energy of activation (Ea)
Some candidates could not write the correct unit by using rate constant method.
along with the answer.

MARKING SCHEME
Question 2
(a) (i) Rate law expression
Rate = k [A]1 [B]2 [C]0 OR Rate = k [A]1 [B]2
(ii) Rate of reaction will increase 8 times if the concentration of A, B and C are doubled.
OR
(b) T 1 = 293 K
T 2 = 313 K
K2 / K1 = 4
R = 8·314 J K-1 mole-1
14
𝐾𝐾 𝐸𝐸𝑒𝑒 𝑇𝑇 −𝑇𝑇
Log 𝐾𝐾2 = � 𝑇𝑇2 𝑇𝑇 1�
1 2·303𝑅𝑅 1 2
𝐸𝐸𝑒𝑒 313−293
Log 4 = �
2·303×8·314 293×313

𝐸𝐸𝑒𝑒 20
0·6021 = 19·147 �91709� = 52862·94 J / mol or 52·863 kJ / mol

[2]
Question 3
(a) How do antiseptics differ from disinfectants?
(b) State the role of the following chemicals in the food industry:
(i) Sodium benzoate
(ii) Aspartame

Comments of Examiners
(a) The difference between antiseptics and disinfectants Suggestions for teachers
was not brought out clearly by most of the candidates.
Also, the examples given by many candidates were − Encourage students to read the Unit:
Chemistry in Everyday life. The use
not correct.
of chemicals in medicine should be
(b) (i) A few candidates could not write the role of illustrated to the students with suitable
Sodium benzoate in the food industry. examples.
(ii) For aspartame, some candidates wrote that it is − Discuss the use of various chemicals in
used as a flavouring agent instead of an the food industry with suitable
artificial sweetening agent. examples.

MARKING SCHEME
Question 3
(a) Antiseptics Disinfectants
(i) These chemicals prevent the growth of (i) These chemicals destroy the
micro-organism or may even kill them microorganism but are harmful for
without affecting the living tissues. living tissues.
(ii) They are applied to living tissues such (ii) They are generally used to kill
as ulcers, wounds, diseased stem microorganisms and are applied to
surface. inanimate objects like floor, toilets.
(Any one difference for each. An example will not be accepted as a difference.)
(b) (i) Sodium benzoate: Food preservative
(ii) Aspartame: artificial sweetening agent

[2]

15
Question 4
An aromatic organic compound [A] on heating with NH 3 and Cu 2 O at high pressure gives [B].
The compound [B] on treatment with ice cold solution of NaNO 2 and HCl gives [C], which on
heating with Cu/HCl gives compound [A] again. Identify the compounds [A], [B] and [C].
Write the name of the reaction for the conversion of [B] to [C].

Comments of Examiners
Compounds (A) (B) and (C) were identified correctly Suggestions for teachers
by most of the candidates. A few candidates wrote (A)
as benzene instead of chlorobenzene and (C) as − Give ample practice for conversion of
chlorobenzene instead of benzenediazonium chloride. Organic compounds.
Some candidates wrote the name of the reaction as − Teach named organic reactions with
Sandmeyer’s reaction instead of Diazotisation reaction. proper conditions.

MARKING SCHEME
Question 4
Cl
(A) O Or C6H5Cl or Chlorobenzene
NH2
(B) O Or C6H5NH2 or Aniline

N2Cl
(C) O Or C6H5N2Cl or Benzenediazonium chloride
Diazotisation reaction

[2]
Question 5
Write the names of the monomers for each of the following polymers:
(a) Bakelite
(b) Nylon – 2 – nylon – 6

16
Comments of Examiners
(a) The monomers of bakelite were named correctly by
most candidates. A few candidates wrote benzene Suggestions for teachers
instead of phenol and acetaldehyde instead of
− Teach the correct pair of monomers to
formaldehyde. students. Give practice in writing
(b) Monomers of Nylon – 2 – nylon - 6 were not written names and structures of monomers and
correctly by most of candidates. Many candidates units of polymers.
wrote monomers of Nylon 6 (i.e. caprolactum) or − Elucidate biodegradable and non-
monomers of nylon 6, 6 (i.e. ethylene diamine and biodegradable polymers in class in
adipic acid) instead of monomers of Nylon - 2 nylon - detail.
6 (i.e. glycine and 5-aminocaproic acid).

MARKING SCHEME
Question 5
(a) Bakelite: phenol and formaldehyde
(b) Nylon – 2 – nylon – 6: glycine and 5 – aminocaproic acid

Question 6 [2]

Name the purine bases and pyrimidine bases present in RNA and DNA.

Comments of Examiners
Suggestions for teachers
Many candidates did not specify the purine and the
pyrimidine bases of DNA and RNA. They combined and Teach structure of RNA and DNA with
wrote all the bases. proper purines and pyrimidine bases
along with diagrams.

MARKING SCHEME
Question 6
DNA RNA
Purine bases Adenine and guanine Adenine and guanine
Pyrimidine bases Thymine and cytosine Uracil and cytosine

17
Question 7 [2]
(a) How will you obtain the following? (Give balanced equation.)
(i) Picric acid from phenol.
(ii) Ethyl chloride from diethyl ether.
OR
(b) How will you obtain the following? (Give balanced equation.)
(i) Anisole from phenol
(ii) Ethyl acetate from ethanol.

Comments of Examiners
(a)(i)Most of the candidates wrote unbalanced
equations. A few of them did not write Suggestions for teachers
concentrated HNO 3 or concentrated H 2 SO 4 .
− Explain organic reactions and
Some candidates did not write the by-product i.e. conversions with proper reactants,
H 2 O for the conversion of phenol to picric acid. catalysts and conditions.
(ii) For the conversion of C 2 H 5 -O-C 2 H 5 to C 2 H 5 Cl, − More practice should be given for the
some candidates used Cl 2 instead of PCl 5 or conversion of organic compounds with
SOCl 2 . A few candidates did not write the by balanced equations.
− Explain to the students to write the by
product.
product in all organic reactions.
(b) (i) For the conversion of phenol to anisole, many
candidates converted phenol directly by
reacting with CH 3 Br. They did not convert
phenol to phenoxide.
(ii) For the conversion of ethanol to ethyl acetate, most of the candidates wrote incorrect structure
of the product. Some candidates did not balance the equation.

MARKING SCHEME
Question 7
(a) (i)
OH 𝑐𝑐𝑜𝑜𝑐𝑐𝑐𝑐. 𝐶𝐶2 𝑆𝑆𝐶𝐶4 OH
O + 3HNO3 O2N O NO2 + 3H2O
conc. NO2
(ii) C 2 H 5 OC 2 H 5 + PCl 5 → 2C 2 H 5 Cl + POCl 3
or
C 2 H 5 OC 2 H 5 + SOCl 2 → 2C 2 H 5 Cl + SO 2

18
OR
ONa OCH3

(b) (i) OH
𝑁𝑁𝑒𝑒𝑂𝑂𝐻𝐻 𝐶𝐶𝐻𝐻3 𝐵𝐵𝑟𝑟
O O O + NaBr
−𝐻𝐻2 𝑂𝑂 ∆
Anisole
𝑐𝑐𝑐𝑐𝑛𝑛𝑐𝑐
(ii) C 2 H 5 OH + CH 3 COOH CH 3 COOC 2 H 5 + H 2 O
𝐻𝐻2 𝑆𝑆𝑂𝑂4
Or
C 2 H 5 OH + CH 3 COCl → CH 3 COOC 2 H 5 + HCl
Or
C 2 H 5 OH + (CH 3 CO) 2 O → CH 3 COOC 2 H 5 + CH 3 COOH

Question 8 [2]

40% of a first order reaction is completed in 50 minutes. How much time will it take for the
completion of 80% of this reaction?

Comments of Examiners
Most of the candidates calculated the answer by using the Suggestions for teacher
unitary method instead of using the appropriate formula. − Give more practice in numerical
Some candidates substituted the value of (a-x) as 40 problems based on order reaction.
Emphasise on step by step calculations to
instead of 60. Some candidates reported the time in
calculate the value of k and t.
seconds which was not required.
− Train students to solve problems in a step
by step manner: formula substitution
calculation answer with unit.

MARKING SCHEME
Question 8
2·303 𝑒𝑒
k= log10 𝑒𝑒−𝑥𝑥
𝑒𝑒
2·303 100
= 50
log 60
2·303
k = 50 × 0 · 2218
k = 0·0102 min-1
2·303 100
t = 𝑘𝑘 log 20
2·303
t = 0·0102 × 0 · 6989
t = 157·8 min

19
[3]
Question 9
(a) The freezing point of a solution containing 5·85g of NaCl in 100 g of water is −3·348 oC.
Calculate van’t Hoff factor ‘i’ for this solution.What will be the experimental molecular
weight of NaCl?
(K f for water = 1·86 K kg mol-1, at. wt. Na = 23, Cl = 35·5)
OR
(b) An aqueous solution containing 12·48g of barium chloride (BaCl 2 ) in 1000 g of water, boils
at 100·0832oC. Calculate the degree of dissociation of barium chloride. (K b for water
= 0·52 K kg mol-1, at. wt. Ba = 137, Cl = 35·5)

Comments of Examiners
(a) Most candidates calculated the value of van’t Hoff
factor (i) correctly but some failed to calculate the Suggestions for teachers
value of experimental molecular weight of NaCl.
(b) Most of the candidates calculated the correct value of − Teach abnormal molecular weight,
van’t Hoff factor (i) but they were not able to calculate using van’t Hoff factor (i) along with
the number of particles formed after ionisation of degree of dissociation/ association
BaCl 2 i.e. comprehensively to the students.
BaCl 2 Ba2+ + 2Cl-, n=3 − Give more practice in numerical
problems based on van’t Hoff factor.
They were not able to substitute the value of ‘n’
correctly in the formula, hence, degree of dissociation
of BaCl2 was not calculated correctly.

MARKING SCHEME
Question 9
(a) ∆𝐶𝐶𝑓𝑓 = 𝑖𝑖 𝐾𝐾𝑓𝑓 × 𝑚𝑚
𝑤𝑤𝐵𝐵 ×1000
Or ∆𝐶𝐶𝑓𝑓 = 𝑖𝑖 𝐾𝐾𝑓𝑓 × 𝑚𝑚𝐵𝐵 ×𝑤𝑤𝐴𝐴
5·85×1000
3·348 = 𝑖𝑖 × 1 · 86 × 58·5×100
3·348
∴ 𝑖𝑖 = 1·86
=1·8
𝑛𝑛𝑐𝑐𝑟𝑟𝑚𝑚𝑒𝑒𝑛𝑛 𝑚𝑚𝑐𝑐𝑛𝑛𝑒𝑒𝑐𝑐𝑚𝑚𝑛𝑛𝑒𝑒𝑟𝑟 𝑤𝑤𝑒𝑒𝑤𝑤𝑤𝑤ℎ𝑒𝑒
𝑖𝑖 = 𝑒𝑒𝑥𝑥𝑒𝑒𝑒𝑒𝑟𝑟𝑤𝑤𝑚𝑚𝑒𝑒𝑛𝑛𝑒𝑒𝑒𝑒𝑛𝑛 𝑚𝑚𝑐𝑐𝑛𝑛𝑒𝑒𝑐𝑐𝑚𝑚𝑛𝑛𝑒𝑒𝑟𝑟 𝑤𝑤𝑒𝑒𝑤𝑤𝑤𝑤ℎ𝑒𝑒
𝑛𝑛𝑐𝑐𝑟𝑟𝑚𝑚𝑒𝑒𝑛𝑛 𝑚𝑚𝑐𝑐𝑛𝑛𝑒𝑒𝑐𝑐𝑚𝑚𝑛𝑛𝑒𝑒𝑟𝑟 𝑤𝑤𝑒𝑒𝑤𝑤𝑤𝑤ℎ𝑒𝑒
∴ 𝐸𝐸𝐸𝐸𝐸𝐸𝐸𝐸𝑜𝑜𝑖𝑖𝑚𝑚𝐸𝐸𝑐𝑐𝐸𝐸𝐸𝐸𝐸𝐸 𝑚𝑚𝑜𝑜𝐸𝐸𝐸𝐸𝑐𝑐𝑚𝑚𝐸𝐸𝐸𝐸𝑜𝑜 𝑤𝑤𝐸𝐸𝑖𝑖𝑤𝑤ℎ𝐸𝐸 = 𝑤𝑤

58·5
or = 1·8
= 32·5 g mol-1
OR
o
(b) w2 = 12·48 g, Ts = 100·0832 C
w1 = 1000 g, Kb for water = 0·52 K mol-1
M2 (BaCl2) = 208
20
∆ Tb = Ts–To
= 100·0832 – 100
= 0·0832oC
1000 𝐾𝐾𝑏𝑏 𝑤𝑤2
M2=
∆ 𝑇𝑇 ×𝑤𝑤 𝑏𝑏 1
1000×·52×12·48
=
0·0832×1000

=78g mol-1
𝑛𝑛𝑐𝑐𝑟𝑟𝑚𝑚𝑒𝑒𝑛𝑛 𝑚𝑚𝑐𝑐𝑛𝑛𝑒𝑒𝑐𝑐𝑚𝑚𝑛𝑛𝑒𝑒𝑟𝑟 𝑤𝑤𝑒𝑒𝑤𝑤𝑤𝑤ℎ𝑒𝑒
i = 𝑐𝑐𝑜𝑜𝑜𝑜𝑒𝑒𝑟𝑟𝑜𝑜𝑒𝑒𝑜𝑜 𝑚𝑚𝑐𝑐𝑛𝑛𝑒𝑒𝑐𝑐𝑚𝑚𝑛𝑛𝑒𝑒𝑟𝑟 𝑤𝑤𝑒𝑒𝑤𝑤𝑤𝑤ℎ𝑒𝑒
208
= = 2·666 or 2·67
78

BaCl2 → Ba+2 + 2Cl− (3 ions)


𝑤𝑤−1 2·67−1 1·67
𝛼𝛼 = 𝑛𝑛−1 = 3−1 = 2 = 0 · 835 or 83·5%

[3]
Question 10
Examine the defective crystal given below and answer the question that follows:
A+ B- A+ B- A+
B- B- A+ B-
A+ B- A+ A+
B- A+ B- A+ B-

State if the above defect is stoichiometric or non-stoichiometric. How does this defect affect the
density of the crystal? Also, write the term used for this type of defect.

Comments of Examiners
Most of the candidates were able to answer this part
correctly. Some candidates wrote non- stoichiometric Suggestions for teachers
instead of stoichiometric defect. The density of crystal
should decrease but some candidates wrote that there Explain various types of imperfections
would be no change in density. The term used for this in solids to students. Also discuss how
these imperfections affect the properties
type of defect was Schottky defect, but some candidates
of the crystal.
wrote it as Frenkel defect.

21
MARKING SCHEME
Question 10
The defect is stoichiometric (because equal number of cations and anions are missing from
lattice sites.)
It lowers the density of the crystal.
Schottky Defect.

Question 11 [3]
Give reason for each of the following:
(a) For ferric hydroxide sol the coagulating power of phosphate ion is more than chloride
ion.
(b) Medicines are more effective in their colloidal form.
(c) Gelatin is added to ice creams.

Comments of Examiners
(a) Most of the candidates did not write the correct
Suggestions for teachers
reason. Many did not use Hardy Schulze law to
explain the answer. − Familiarise students with different
laws/ principles/ key concepts and their
(b) Many candidates gave incorrect reason regarding applications thoroughly, especially
effectiveness of medicines in their colloidal form. those which are useful in our daily
(c) This part was also answered incorrectly by many lives.
candidates. Quite a few wrote that it acts as a − Give more practice to students in
answering reasoning type questions.
flavouring or a sweetening agent.

MARKING SCHEME
Question 11
(a) According to Hardy-Schulze law, phosphate ion has more negative charge as compared to
chloride ion.
(b) Assimilation is easy due to their colloidal size.
(c) Gelatin when added to ice creams acts as an emulsifier and helps to stabilise the emulsion.
(Protective colloid).

22
[3]
Question 12
(a) For the complex ion [Fe(CN)6]3- , state:
(i) the type of hybridisation.
(ii) the magnetic behaviour.
(iii) the oxidation number of the central metal atom.
(b) Write the IUPAC name of [Co(en)2Cl2]+ ion and draw the structures of its geometrical
isomers.

Comments of Examiners
(a) For the complex ion [Fe(CN)6]3-: Suggestions for teachers
2 3
(i) the type of hybridisation was d sp but some − Explain the method to determine the
candidates wrote sp3d2 hybridization. type of hybridization, magnetic
(ii) the magnetic behaviour of [Fe(CN)6]3- was behaviour and Oxidation state, by
paramagnetic but a few candidates wrote using valence bond theory.
− Discuss strong field, weak field,
diamagnetic behavior. ligands, low spin complexes and high
(iii) many candidates wrote oxidation state of spin complexes with magnetic
central metal as +6 or -3 instead of +3. behaviour with students.
(b) Most of the candidates were unable to write the − Teach the rules of nomenclature of
correct IUPAC name of the complex compound. coordination compounds in detail and
They did not write the correct alphabetic order in give adequate practice. Explain
case of name of Ligands. Oxidation number of Geometrical isomers with examples.
central metal atom was not calculated correctly.
Most of the candidates were unable to draw the
structures of geometrical isomers.

MARKING SCHEME
Question 12
(a) (i) d2sp3
(ii) Paramagnetic
(iii) +3
(b) dichloridobis(ethylenediamine) cobalt (III) ion

+ Cl
en + en +
Cl Cl
or Co en
Co en Co

Cl en
Cl
en
Cl
d-form
l-form transform

Cis
23
[3]
Question 13
(a) Explain why:
(i) Mn2+ is more stable than Fe2+ towards oxidation to +3 state.
(At. no. of Mn = 25, Fe = 26)
(ii) Transition elements usually form coloured ions.
(iii) Zr and Hf exhibit similar properties.
(At. no. of Zr = 40, Hf = 72)
OR
(b) Complete and balance the following chemical equations:
(i) KMnO4 + KI + H2SO4 → _____ + ______ + ______ + _______
(ii) K2Cr2O7 + H2SO4 + H2S → _____ + ______ + ______ + _______
(iii) KMnO4 + H2SO4 + FeSO4 → _____ + ______ + ______ + _______

Comments of Examiners
(a) (i) Many candidates wrote only the electronic
configuration of Mn2+ and Fe2+ but they could not Suggestions for teachers
explain the reason for the stability of Mn2+
− Explain properties of d Block
towards oxidation to + 3 state. elements in detail with the help of
(ii) Some candidates explained that formation of Orbital diagrams and suitable
coloured ions of transition elements was due to examples. Keywords such as d-d
vacant ‘d’ orbital or partially filled ‘d’ orbital transition, half-filled sub shells,
which was incorrect. stability, etc. must be explained. Also
explain Lanthanide contraction and
(iii)Most candidates were not able to give the reason
its consequences.
for Zr and Hf exhibiting similar properties.
− Give more practice in writing
(b) Unbalanced/ partially balanced/ incorrect equations complete and correctly balanced
were given by many candidates. Some candidates chemical equations. Student should
wrote incorrect formulae of products such as be explained the oxidising and
Mn(SO4)2 instead of MnSO4, Cr(SO4)3 instead of reducing properties of K2 Cr2 CO7 and
Cr2(SO4)3 and Fe2SO4 instead of Fe(SO4)3. KMn O4

MARKING SCHEME
Question 13
(a) (i) Electronic configuration of Mn+2 is 3d5, which is half filled and hence stable. Hence,
it cannot lose third electron easily. In case of Fe+2 electronic configuration is 3d6.
Hence,it can lose one electron easily to give stable configuration 3d5.
(ii) It is due to d – d transition by absorbing part of visible light.

24
(iii) Due to Lanthanoid contraction they have same atomic and ionic size. or They have
same general electronic configuration.
OR
(b) (i) 2KMnO4 + 10KI + 8H2SO4 → 6K2SO4 + 2MnSO4 + 5I2 + 8H2O
(ii) K2Cr2O7 +4H2SO4 + 3H2S → K2SO4 + Cr2(SO4)3 + 3S + 7H2O
(iii) 2KMnO4 +8H2SO4 + 10FeSO4 → K2SO4+2MnSO4+5Fe2(SO4)3+8H2O

Question 14 [3]

(a) Arrange the following in the increasing order of their basic strength:
C2H5NH2 , C6H5NH2 , (C2H5)2NH
(b) Give a balanced chemical equation to convert methyl cyanide to ethyl alcohol.
(c) What happens when benzene diazonium chloride reacts with phenol in weak alkaline
medium? (Give balanced equation).

Comments of Examiners
(a) Instead of writing in increasing order of basic strength, Suggestions for teachers
a few candidates wrote the answer in decreasing order. − Explain clearly giving reasons how
Some candidates wrote incorrect order such as the basic strength of amines increases
C2H5NH2 < C6H5NH2 < (C2H5)2NH instead of or decreases.
C6H5NH2 < C2H5NH2 < (C2H5)2NH. − Insist upon learning conversion of
(b)Many candidates converted methyl cyanide to acetic one organic compound to other
acid or methyl cyanide to ethyl amine instead of and give ample practice in writing
methyl cyanide to ethyl alcohol. Many candidates did balanced chemical equations with
not write the by-product. proper conditions/reagents.
(c) The reaction of benzene diazonium chloride with − Instruct students to read the
phenol in weak alkaline medium was not written by observations of different organic
many candidates. Some candidates were neither able reactions with colour or precipitate.
to write the correct product nor able to write the colour Diazotisation, formation of azo dye
of the dye. Only a few could write the correct balanced should be explained properly to
students.
equation.

25
MARKING SCHEME
Question 14
(a) The increasing order of basic strength given organic compounds:
C6H5NH2 <C2H5NH2 < (C2H5)2NH
(b) 𝐶𝐶𝐶𝐶3 − 𝐶𝐶 ≡ 𝐶𝐶
4[𝐻𝐻]
𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶2 𝐶𝐶𝐶𝐶2
𝐻𝐻𝑁𝑁𝑂𝑂2
𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶2 𝐶𝐶𝐶𝐶 + 𝐶𝐶2 + 𝐶𝐶2 𝐶𝐶
𝐿𝐿𝑤𝑤𝐿𝐿𝑛𝑛𝐻𝐻4
or
𝐶𝐶𝐸𝐸 ⁄𝐶𝐶2 𝐶𝐶5 𝐶𝐶𝐶𝐶
𝑁𝑁𝑤𝑤𝑐𝑐𝑟𝑟𝑁𝑁𝑒𝑒 𝐻𝐻𝑁𝑁𝑂𝑂2
Or 𝐶𝐶𝐶𝐶3 − 𝐶𝐶 ≡ 𝐶𝐶 + 2𝐶𝐶2 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶2 𝐶𝐶𝐶𝐶2 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶2 𝐶𝐶𝐶𝐶 + 𝐶𝐶2 ↑ +𝐶𝐶2 𝐶𝐶

(c)
𝑂𝑂𝐻𝐻 −
O N2Cl + H O OH O N=N O OH + HCl
P-hydroxyazobenzene
(Orange dye)
[3]
Question 15
Name the sulphide ore of Copper. Describe how pure copper is extracted from this ore.

Comments of Examiners
Name of copper ore was mentioned correctly by most of Suggestions for teachers
the candidates. However, extraction of copper from the
− Advise students to learn metallurgy in
sulphide ore was not given stepwise by many candidates.
detail.
Quite a few wrote the name of process such as Roasting,
− Explain principles and process of
Smelting, Bessemerisation without giving the details and
isolation of metals with the help of
the chemical equation/s involved. Some forgot to write
flowcharts.
“electro refining”.
− Interpret the extraction of metal with
proper steps like concentration,
roasting, smelting, etc. with complete
balanced equations involved. The
process of refining should also be
illustrated completely.

26
MARKING SCHEME
Question 15
The sulphide ore of copper is:
Chalcopyrite / copper pyrite / CuFeS2
Extraction of pure copper from its ore:
Froth flotation process
Roasting – concentrated ore is heated with excess of air or oxygen.
2CuFeS2 + O2 → Cu2S + 2FeS + SO2↑
Smelting – Roasted ore is mixed with coke and sand and fed into the
blast furnace.
2Cu2S + 3O2 → 2Cu2O + 2SO2
2FeS + 3O2 → 2FeO + 2SO2
FeO + SiO2 → FeSiO3
Auto reduction takes place in Bessemer Converter or Bessemerisation
2Cu2O + Cu2S → 6Cu + SO2↑
Blister Copper
Electrorefining gives pure Cu (99·9%)
(either equation or statement)

[5]
Question 16
(a) (i) Calculate the emf and ∆𝐺𝐺 𝑐𝑐 for the cell reaction at 25oC:
2+ 2+
Zn(s)�𝑍𝑍𝑐𝑐(𝑒𝑒𝑎𝑎) � �𝐶𝐶𝐶𝐶(𝑒𝑒𝑎𝑎) � 𝐶𝐶𝐶𝐶(𝑜𝑜)
( 0·1M) (0·01M)

Given 𝐸𝐸 𝑐𝑐 𝑍𝑍𝑐𝑐2+ ⁄𝑍𝑍𝑐𝑐 = −0 · 763 𝐸𝐸𝑐𝑐𝐶𝐶 𝐸𝐸 𝑐𝑐 𝐶𝐶𝐶𝐶2+ ⁄𝐶𝐶𝐶𝐶 = −0 · 403 𝑉𝑉


(ii) Define the following terms:
(1) Equivalent conductivity
(2) Corrosion of metals
OR
(b) (i) The specific conductivity of a solution containing 5 g of anhydrous BaCl2 (mol. wt.
= 208) in 1000 cm3 of a solution is found to be 0·0058 ohm-1cm-1. Calculate the
molar and equivalent conductivity of the solution.
(ii) What is an electrochemical series? How is it useful in predicting whether a metal
can liberate hydrogen from acid or not?

27
Comments of Examiners
(a) (i) A few candidates calculated the value of E°cell with
negative sign i.e. - 0.36 V instead of +0. 36 V. Suggestions for teachers
Many candidates wrote incorrect formula for Nernst
equation. Instead of calculating ∆ G°, some − Give adequate practise in solving
candidates calculated ∆ G which was not asked. numerical problems based on Nernst
(ii) (1) Many candidates wrote incorrect definition of equations
equivalent conductivity or wrote an incorrect − Explain the relationship between
formula and its relationship with specific Gibbs free energy, G°, E°cell and
conductance. differences between G° and G
(2) Some candidates wrote the definition of rusting clearly.
instead of corrosion of metals. − Teach definitions of equivalent
conductivity and corrosion of metal to
(b) (i) The values of molar conductivity and equivalent
the students. Also explain the related
conductivity of the solution were calculated key concepts like factors affecting
correctly but the answer with correct unit was not corrosion and prevention of
given by most of the candidates. corrosion.
(ii)Most candidates wrote the definition of metal − Give practice in numerical problems
activity series instead of electrochemical series. based on specific conductance, molar
Some candidates wrote that metals above conductance and equivalent
hydrogen can liberate hydrogen gas from acid. conductance.
They did not write the answer in terms of reduction − Instruct students to define
potential value. electrochemical series in term of
standard reduction potential values of
elements.

MARKING SCHEME
Question 16
(a) (i) 0 0 0
𝐸𝐸𝑐𝑐𝑒𝑒𝑛𝑛𝑛𝑛 = 𝐸𝐸𝑐𝑐𝑒𝑒𝑒𝑒ℎ𝑐𝑐𝑜𝑜𝑒𝑒 − 𝐸𝐸𝑒𝑒𝑛𝑛𝑐𝑐𝑜𝑜𝑒𝑒
= −0·403 – (−0·763)
= 0·36 V

0
0 · 0591 [𝑍𝑍𝑐𝑐+2 ]
𝐸𝐸𝑐𝑐𝑒𝑒𝑛𝑛𝑛𝑛 = 𝐸𝐸𝑐𝑐𝑒𝑒𝑛𝑛𝑛𝑛 − log
𝑐𝑐 [𝐶𝐶𝐶𝐶+2 ]
Or
0·0591 0·1
𝐸𝐸𝑐𝑐𝑒𝑒𝑛𝑛𝑛𝑛 =0·36 − 2
log 0·01

28
𝐸𝐸𝑐𝑐𝑒𝑒𝑛𝑛𝑛𝑛 =0·36 − 0·0295 log 10
= 0·36 − 0·0295 ×1
= 0·3305 V
∆𝐺𝐺 0 = −𝑐𝑐 𝐹𝐹 𝐸𝐸 0
= −2 × 96,500 × 0 · 36
= −69480 J /mol
= −69 · 48 kJ/mol
(ii) (1) Equivalent Conductivity of Electrolyte – is the conducting power of all the ions
produced by dissolving one-gram equivalent in V cc. of solution.

(2) Corrosion of metals– The slow and spontaneous process of the conversion of a metal
into an undesirable compound (usually oxide) on exposure to atmospheric
conditions is called corrosion of metals.

OR
𝑆𝑆𝑒𝑒𝑟𝑟𝑒𝑒𝑛𝑛𝑤𝑤𝑒𝑒ℎ 𝑐𝑐𝑓𝑓 𝐵𝐵𝑒𝑒𝐶𝐶𝑛𝑛2 5
Molarity of BaCl2 = 𝑀𝑀𝑐𝑐𝑛𝑛𝑒𝑒𝑐𝑐𝑚𝑚𝑛𝑛𝑒𝑒𝑟𝑟 = = 0 · 024 𝑀𝑀
𝑤𝑤𝑒𝑒𝑤𝑤𝑤𝑤ℎ𝑒𝑒 208
1000
Molar conductivity (^𝑚𝑚) = 𝑠𝑠𝐸𝐸𝐸𝐸𝑐𝑐𝑖𝑖𝑠𝑠𝑖𝑖𝑐𝑐 𝑐𝑐𝑜𝑜𝑐𝑐𝐶𝐶𝑚𝑚𝑐𝑐𝐸𝐸𝑖𝑖𝑐𝑐𝑖𝑖𝐸𝐸𝑐𝑐 × 𝑚𝑚𝑐𝑐𝑛𝑛𝑒𝑒𝑟𝑟𝑤𝑤𝑒𝑒𝑚𝑚
0·0058×1000
Molar conductivity (^𝑚𝑚) = 𝑀𝑀𝑐𝑐𝑛𝑛𝑒𝑒𝑟𝑟𝑤𝑤𝑒𝑒𝑚𝑚
or
0·0058×1000
Molar conductivity (^𝑚𝑚) = 0·024
= 241·67 ohm-1 cm2 mol-1
208
Equivalent weight of BaCl2 = 2 = 104
5
Normality of BaCl2 = 104 = · 048 𝐶𝐶
𝑜𝑜𝑒𝑒𝑒𝑒𝑐𝑐𝑤𝑤𝑓𝑓𝑤𝑤𝑐𝑐 𝑐𝑐𝑐𝑐𝑛𝑛𝑜𝑜𝑚𝑚𝑐𝑐𝑒𝑒𝑤𝑤𝑜𝑜𝑤𝑤𝑒𝑒𝑚𝑚 ×1000
Equivalent conductivity(˄𝑒𝑒𝑎𝑎 ) = 𝑁𝑁𝑐𝑐𝑟𝑟𝑚𝑚𝑒𝑒𝑛𝑛𝑤𝑤𝑒𝑒𝑚𝑚
Or
0 · 0058 × 1000
˄𝑒𝑒𝑎𝑎 =
0 · 048
˄ 𝑒𝑒𝑎𝑎 = 120 · 83 ohm-1 cm2 eq-1
When various electrode systems are arranged in the order of their Eo values, the series obtained is
called electrochemical series. Elements having negative value of Eo will liberate H2 from acids.
(or any correct definition)

[5]
Question 17
(a) (i) Explain why:
(1) Nitrogen does not form pentahalides.
(2) Helium is used for filling weather balloons.

29
(3) ICl is more reactive than I2.
(ii) Draw the structures of the following:
(1) HClO4
(2) H3PO3
OR
(b) (i) Explain why:
(1) Mercury loses its meniscus in contact with ozone.
(2) Halogens are coloured and the colour deepens on moving down in the
group from fluorine to iodine.
(3) Hydride of sulphur is a gas while hydride of oxygen is a liquid.
(ii) Complete and balance the following reactions:
(1) NaCl + MnO2 + H2SO4 → _______ + _______ + ________ + _____
(2) KMnO4 + SO2 + H2O → _______ + _______ + __________

Comments of Examiners
(a)(i) (1) Most of the candidates did not mention the
absence of d orbital in nitrogen. Suggestions for teachers
(2) Some candidates wrote that Helium is a − Explain the electronic configuration
noble gas but did not write that it is light,
and properties of p-block elements
inert and non-inflammable.
with reasons for variable valency.
(3) Many candidates wrote that chlorine is
− Explain property of noble gases in
more electronegative, but they did not
detail.
mention that I-Cl bond is weaker than I-I
Bond. − Guide students that inter halogen
(ii) (1) Many candidates drew correct structure of compounds are more reactive due to
HClO4 but a few showed the bond between differences in electronegativity of
H and Cl instead of H and O(oxygen), atoms. They have low bond
which was not correct. dissociation energy hence, more
(2) Many candidates drew incorrect structure - reactive.
they showed three bonds between -OH and − Show structure of oxyacids of
P (phosphorus). halogens, sulphur and phosphorus in
(b)(i) (1) Mercury losses it meniscus due to tailing of class.
Mercury or formation of mercurous oxide - − Teach characteristic properties of
this was not specified by most of the p- block elements in detail.
candidates. − Instruct students to write complete
(2) The absorption of light in visible region and balanced equations giving names
depends upon size of halogen atoms - this of the reactant/s and product/s.
fact was not reported by many candidates.

30
(3) Some candidates did not explain the answer in terms of intermolecular hydrogen bonding.
(ii) Many candidates wrote incomplete/incorrect or unbalanced equations.

MARKING SCHEME
Question 17
(a) (i) (1) Due to the absence of d-orbitals in its valence shell, nitrogen does not form
pentahalides.
(2) Helium being inert, non-inflammable and light gas is used in filling weather
balloons.
(3) I –Cl bond is weaker than I – I bond. I – Cl bond breaks easily to form halogen
atoms (I and Cl)
(ii) (1)
O O
HClO4 ↑ ||
H ─ O ─Cl→ O or H ─ O ─ Cl = O
↓ ||
O O
(2)
O O
H3PO3 ║
H ─ O ─ P ─ H or H─O ─ P ─H
│ │
O O
│ │
H H

OR
(b) (i) (1) Mercury in presence of ozone is oxidised to sub oxide (Mercurous oxide) which
dissolves in mercury. It starts sticking to glass and loses meniscus (Tailing of
Hg).
Or 2Hg + O3 → Hg2O + O2
(2) Halogens are coloured due to absorption of light in visible region. Fluorine
being small absorbs violet colour and shows the complementary colour yellow
whereas iodine absorbs yellow colour and shows complementary colour violet.
(3) Due to small size of oxygen atom H2O forms intermolecular H-bond and gets
associated hence occurs as liquid. While H2S is simple covalent compound
hence occurs as a gas.
(ii) (1) 2NaCl + MnO2 + 3H2SO4 → 2NaHSO4+ MnSO4 + Cl2 + 2H2O
OR 2NaCl + MnO2 + 2H2SO4 → 2Na2SO4+ MnSO4 + Cl2 + 2H2O
(2) 2KMnO4 + 5SO2+2H2O → K2SO4 +2MnSO4 + 2H2SO4

31
[5]
Question 18
(a) (i) Give balanced equations for the following reactions:
(1) Benzaldehyde reacts with hydrazine.
(2) Acetic acid reacts with phosphorous pentachloride.
(3) Acetone reacts with sodium bisulphite.
(ii) Give one chemical test each to distinguish between the following pairs of
compounds:
(1) Ethanol and acetic acid
(2) Acetaldehyde and benzaldehyde
OR
(b) (i) Write chemical equations to illustrate the following name reactions:
(1) Clemmensen’s reduction
(2) Rosenmund’s reduction
(3) HVZ reaction

(ii) Explain why:


(1) Acetaldehyde undergoes aldol condensation, but formaldehyde does not.
(2) Acetic acid is a weaker acid as compared to formic acid.

32
Comments of Examiners
(a)(i)(1) Many candidates wrote incorrect formulae of
reactants and product.
(2) For the reaction of acetic acid with phosphorus Suggestions for teachers
pentachloride, most of the candidates gave − Give sufficient practice in writing
correct equation. organic equations, with name of
(3) Some candidates did not write the correct formula reactants, products and correct
of product for the reaction of acetone with sodium structure.
bisulphite.
(ii) (1) Iodoform test was mentioned for distinguishing − Tell students that the given chemical
ethanol from acetic acid but the observation was test should be positive for one
not written by many candidates. Some candidates compound and negative for the other
mentioned esterification test to distinguish compound.
between ethanol and acetic acid, but this test is − Instruct students to learn the named
given by both the compounds. organic reactions with the name of
(2) Some candidates wrote Tollen’s reagent test to specific catalyst used in the reaction
distinguish between acetaldehyde and and other necessary conditions in the
benzaldehyde - this is given by both the presence of which the required
compounds. product/s is/are formed.
(b)(i) (1) A few candidates wrote unbalanced equations.
Some wrote H2 instead of [H]. Several candidates − Teach mechanism of Aldol
condensation to clear the concept of
did not write Zn/Hg and concentrated HCl. Many
the presence of α - H in CH3CHO.
candidates did not write the by-product.
− Explain the strength of acid and base
(2) Many candidates wrote nascent hydrogen [H] with the help of inductive effect.
instead of H2 or did not write the catalyst.
(3) Some candidates did not write the by product.

33
MARKING SCHEME
Question 18
(a) (i) (1) H
H │
│ C6H5 ─ C = N.NH2+H2O
C6H5 ─ C = O + NH2.NH2 → Benzaldehyde hydrazone
(2)
O O
║ ║
CH3 ─ C ─ OH+ PCl5 → CH3 ─ C ─ Cl+ POCl3+ HCl

(3)
CH3 CH3 OH
C = O + NaHSO3 → C
CH3 CH3 SO3Na

(ii) (1) Ethanol + I2 + Alkali



Yellow precipitate of Iodoform,
acetic acid does not respond to this test.
or
Acetic acid + neutral FeCl3 → Blood red coloration,
Ethanol does not respond to this test. (Or any other relevant test)
(2) Acetaldehyde + I2 + Alkali

Yellow precipitate of Iodoform

Or Acetaldehyde + Fehling solution Red precipitate of Cu2O
Benzaldehyde does not respond to the above test. (Or any other relevant test)
OR
(b) (i) (1) Clemmensen’s Reduction:
𝑍𝑍𝑛𝑛−𝐻𝐻𝑤𝑤/𝐻𝐻𝐶𝐶𝑛𝑛
𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶𝐶𝐶 + 4[𝐶𝐶] 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶3 +𝐶𝐶2 𝐶𝐶
or
𝑍𝑍𝑛𝑛−𝐻𝐻𝑤𝑤/𝐻𝐻𝐶𝐶𝑛𝑛
𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶𝐶𝐶𝐶𝐶3 + 4[𝐶𝐶] 𝐶𝐶𝐶𝐶3 𝐶𝐶𝐶𝐶2 𝐶𝐶𝐶𝐶3 + 𝐶𝐶2 𝐶𝐶
(2) Rosenmund’s Reduction:
O H
║ 𝑃𝑃𝐶𝐶 − 𝐵𝐵𝐸𝐸𝑆𝑆𝐶𝐶4 │
R─ C ─ Cl+ H2 R─ C = O + HCl
𝐵𝐵𝑜𝑜𝑖𝑖𝐸𝐸𝑖𝑖𝑐𝑐𝑤𝑤 𝐸𝐸𝑐𝑐𝐸𝐸𝐸𝐸𝑐𝑐𝐸𝐸

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(3) HVZ reaction:

Cl2 /RedP Cl2 /RedP


CH3COOH CH2ClCOOH CHCl2COOH
−HCl −HCl
−HCl Cl2/RedP

Cl3C. COOH
(ii) (1) Aldol condensation is given by aldehydes having 𝛼𝛼–hydrogen atom.
Acetaldehyde has 𝛼𝛼 –H but HCHO does not have 𝛼𝛼 – hydrogen atom.
Hence, does not give aldol condensation.
(2) Acetic acid has methyl (electron releasing) group which causes + I effect and
decreases its acidic strength of acetic acid.

Note: For questions having more than one correct answer/solution, alternate correct answers/solutions,
apart from those given in the marking scheme, have also been accepted.

35
• The packing efficiency of different type of unit cells. Imperfection
in solids.
• Numerical problem based on elevation of boiling point,
Topics depression in freezing point,
found • van’t Hoff factor and degree of dissociation.
difficult by
• Numerical problem related to Arrhenius equation.
candidates
• Rate Law expression order of reaction and half-life period.
• Nernst equation, electrochemical series, equivalent and molar
conductance corrosion of metals.
• Surface chemistry, application of colloids, purification of
colloids.
• Coordination compounds nomenclature, isomerism hybridisation
of coordination compounds.
• Chemical equations of inorganic compounds, extraction of
copper, chemical equations of K2 Cr2 O7 and KMnO4.
• Named organic reactions, conversion of organic compounds
reasoning type of questions of organic chemistry.
• Polymers, Biodegradable Polymers and their examples.
• Use of chemicals in Food Industry, antiseptics and disinfectants.

• Isomerism of coordination compounds (linkage and geometrical)


Concepts in and nomenclature of coordination compounds.
which • Relationship between E°cell and standard free energy change (
candidates G°).
got • Purines and pyrimidines present in RNA and DNA.
confused • Colloidal solution and their applications.
• Reactions of inorganic compounds with balanced equation.
• Tests to distinguish organic compounds.

36
• Be regular and systematic in your studies.
Suggestions • Avoid selective study - questions are asked from every chapter.
for • Name organic compounds preferably using the IUPAC
candidates Nomenclature.
• Always solve the numerical problems stepwise i.e., (a) formula
(b) substitution (c) calculation (d) answer with correct unit.
• Practise adequate number of numerical problems.
• Always write balanced chemical equations with the essential
conditions.
• Learn both positive and negative chemical tests of organic
compounds.
• In each topic, learn the definitions with keywords with proper
understanding. Write the keyword in your answer.
• Read the question paper carefully and understand what is
required before attempting the question.
• Read the full chapter according to the topic given in the scope of
syllabus.
• Do not waste time in attempting extra questions given as internal
choice.
• Stress upon clarifying the concepts of each topic to answer the
reasoning type of questions.

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