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Problem 1 18 marks

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(1)

B, C

H H H

N N N

H

N

+

+ + +

Problem 1 18 marks

Heterocyclic compounds

1.1

1.2

1.3

B.

1.4 a)

b)

Name of Student Roll No.

F > G > E

NH

NH NO2

O3S or HO3S

NO2

I H

(2)

X

or or

1.5

1.6

C.

1.7

1.8 Yes

1.9

S (gives an oxime) T U V

N H O H

N N H O H

H

NH

(C9H11NO) (C9H9N) (C9H7N)

1 mole 2 moles

N H2 O

N H2

H5C2 CHO

+

..

(3)

Problem 2 12 marks Analysis of alloys

A.

2.1

2.2

2.3

2.4

2.5

B.

2.6

2.7

2.8

2.9

C.

NO3

(aq) + 10H+ (aq) + 8e NH4+

(aq) + 3H2O

Fraction of the total current = 36.1%.

Pb2+ (aq) + 2H2O PbO2↓ + 4H+ (aq) + 4e

mmol of PbO2 = 0.0132

Amount of zinc = 0.184 g

2Cu2+ (aq) + 4I (aq) Cu2I2↓ + I2(aq)↑ 2S2O32− (aq) + I2(aq) S4O62 (aq) + 2I(aq) 0.484 g of copper

70%

0.469 g of copper

Relative percentage deviation = 3.1%

Cr2O72− (aq) + 14H+ (aq) + 6I (aq) 2Cr3+ (aq) + 7H2O + 3I2

Molarity of thiosulphate = 0.0485 M

(4)

Problem 3 18 Marks Halogens

3.1 (c )

3.2 (a) (c)

3.3 No

3.4 (a)

(b) (iii) (c)

3.5

3.6

3.7

Solvent Solubility Solvent Solubility

Carbon tetrachloride 19 n-Hexane 13

Diethyl ether 337 Toluene 182

Solvent λmax Color

Carbon tetrachloride 520 - 540 nm Bright violet

Diethyl ether 460 - 480 nm Deep brown

F2 + Br2 → 2BrF (A)

3BrF → Br2(g) + BrF3 (B) or 5BrF → 2Br2(g) + BrF5 (B)

BrF3 + SbF5 [BrF2]+[SbF6] or

BrF5 + SbF5 [BrF4]+[SbF6] KI7 /I7

X X

X X

X

(5)

3.8

3.9 a)

b)

c)

d)

3.10

3.11

Lewis Acid Lewis Base

Reactants SbF5 F

Products BrF2+

/ BrF4+

SbF6

S

12

Tetrahedral

XeO64−

N S

F F

F .. .

. .

. . . .

.. .

Sb

Sb F

F F

F F F

F

F F F F

(6)

X

Problem 4 23 marks

Chemistry of carbocations

4.1

4.2

4.3 i) Yes ii) No iii) Yes 4.4

4.5

4.6 (iii) 4.7 (ii)

4.8

4.9

sp2

IV > III > I > II

C

+

D

+

Br

X

X X

X

(7)

or

(carbocation)

L M N (C13 H21O)

X

X X

4.10 .

4.11

4.12

4.13 (i)

4.14 (i) or (ii) (As per the given structure of P in 4.12)

4.15

and

O O

C H3 O

O

H O

H P

O

J (C17H24O) O

H HO

O H

(8)

Propagation steps: (ii) & (iii) Termination step: (iv)

] Cl [

] H [ k I k ] k [H

] [Cl 2k ] [H ] [Cl k ] ][Cl [H k 2I t 0

d ] d[Cl

].

][Cl [H k ] ][H [Cl k t 0

d ] d[H

2 2 12

3 abs 2 1

2 3 2 1

2 2

abs

2 2

2 1





=

+

=

=

] .[H k I 2K or ] [H ] [I dt k

d[HCl]

1/2 2 3 abs1/2 1 2 2

1 abs

= '

.05 1 Yield

Quantum =

Problem 5 18 marks

The ‘light’ side of chemistry

5.1

5.2

5.3

5.4 The correct statement/s is/are i)

ii) 5.5

B.

5.6 a).

b)

c)

5.7 a)

∆H - ∆H* = NAh (νAOH − νAO)

∆UAOH = NA AOH

∆UAO

= NAAO

∆pka= NAh (νAO − νAOH) /2.303RT X

X

∆U* = ∆UAO+ ∆U −∆UAOH

(9)

1 . ] 0 NH [Pr

] NH [Pr

3 2 =

+

COOH] 0.03 R

N [H

] COO R

N [H

3

2 =

+

Problem 6 11 marks

Acids, bases and buffers A.

6.1

6.2

6.3

B.

6.4

6.5 around point B around point D

6.6

6.7 (iii)

HC2 C H2

HC2

C H2 C H2

C H2 C H2

CH2 C

H2 H2N COO

H3N COO

H3+N COOH

+

X X

08 . 10 pH=

pH ≈ 6

appropriate indicator is –Methyl red. (4.2-6.2)

X

Riferimenti

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