ChemistryAK - kvafsavadistaff

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4

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COMMON PRE-BOARD EXAMINATION 2011-12 SET - III

XII - CHEMISTRY SCORING KEY

Q.NO.

1

VALUE POINTS

Liquid and liquid

2 For one B, two tetra (A:2/3)

MARKS

½ + ½

1

Xanthate - Collector (increases non-wetability of the ore particle)

AgI/Ag + (+ve)

Bi +5 is less stable than Bi +3 (close to

1

1

1

1

1 7

8

6

9

10

Inert pair effect). So undergoes reduction

2-methyl cyclohexane carbaldehyde equation/reaction cellulose-β-glycosidic enzyme not present in human stomach

Starch – α-glycosidic enzyme present in the human stomach i) Association or dissociation of solute particles ii)due to osmosis, fluid retention a) Large surface area increases rate of reactions.

On dilution o/w – no separate layer w/o – separate layer

12 ΔG for the process FeO + C Fe + CO must be negative at 673K ΔG = ∑ 𝐺 0 𝑝𝑟𝑜𝑑𝑢𝑐𝑡𝑠

- ∑ 𝐺

0 𝑟𝑒𝑎𝑐𝑡𝑎𝑛𝑡𝑠

ΔrG 0 = -325 – (-375) = 50 – not possible

At 1073 ΔG 0 r

=-455 - -275 = -175 – possible b) Simultaneous effective collision of many molecules to turn into

product is rare.

11 Dilution test or dye test

½ + ½

½ + ½

1

1

1

1

1

½

½

½

½

13 i) S is sterically protected in SF

6 ii) reacts with atmospheric oxygen to form reddish brown NO

2

.

Or eqn. NO + 1/2O

2

NO

2

14 HCl gets oxidised to Cl

2

by KMnO

4 but H

2

SO

4 does not react

16HCl + 2KMnO

4

5 KCl + 2MnCl

2

+ 5Cl

2

+8H

2

O

Or

A = Dichromate ion Cr

2

O

7

2-

B =Chromate ion CrO

4

2-

CrO

4

2-

H+

Cr

2

O

7

2-

OH -

[ 2CrO

4

2 + 2H + Cr

2

O

7

2+ H

2

O

Cr

2

O

7

2 + OH 2CrO

4

2 + H

2

O ]

15 (i)C

6

H

5

CH(C

6

H

5

)Br due to the higher stability of carbocation formed

(ii)CH

2

=CH-CH

2

I weaker -CI bond

1

1

16 (i) To prevent the formation of toxic phosgene

(carboyl chloride) or correct equation

(ii) Any one reason

CHCl

3

/ NaOH

17 (i) C

6

H

5

OH

Reimer – Tiemann reaction

Ortho and para hydroxy benzaldehyde

½

(ii) C

6

H

5

-OCH

3

CH

3

Cl/ anhyd. AlCl

3

C

6

H

4

(OCH

3

)CH

3

(Ortho and para)

Friedel – crafts alkylation

½

½

1

1

1

1

1

1

1

1/2

1/2

18 (i) propene i.

B

2

H

6 ii. H

2

O

2

/OH -

propan-1-ol

Or

HBr

Propene 1-bromopropane

H

2

O

2

(ii)ethanol

SOCl

2

C

2

H

5

Cl

NaOH

propan-1-ol

Na-CΞCH/ ether

C

2

H

5

-CΞCH

1

1

but-1-yne

𝑍𝑀

19 d:

𝑁

𝐴 𝑎 3

½

For FCC: z=4 ½

Substituting correct values 1/2 agrees with measured value

8.97 gm/cm 3

20 ΔH = -ve

-ve deviation

Labelled graph

One example

21 first order reaction

1

1

½

1

1

½ t=

2.303

𝐾 𝑙𝑜𝑔 𝑎 𝑎−𝑥 or t=

2 .

303 log

K

[ R

0

]

[ R ]

½

K=

0.693

𝑡

1

2

½

0.693

K =

37.9 secs

= 0.0183 s -1 ½

Substitution with correct values 1/2

Correct answer with unit(time) = 75.77 sec. ½

22 (i) H

2

O is a weak ligand. Thus d 7 is stable. With strong ligands, more

CFSE which compensate 3 rd I.E

(ii) High hydration enthalpy of Cu 2+ compensate second I.E value

(iii) Similar size due to intervening lanthanide contraction

23 differentiation – (definition, difference)

Phenol

24 i. Correct, labelled diagram for octahedral co-ordn. No.6; octahedral complex ii. t

2g

4 , e g

0 ½ iii. optical 1/2

25 (i) more p kb means less kb, hence aniline is less basic than ethyl amine.

Non-availability of L.P of electrons of N in aniline due to –R effect of

benzene ring. Or +I effect of alkyl group in ethyl amine increases

availability of electrons

(ii) 3 0 amines do not have an H for displacement on nitrogen atom

1

1

1

1

1

2

1

1 1/2

(iii) Zwitter ion (in neutral) medium is least soluble (in water).

In acids and bases, become soluble form.

26 initiation peroxide +ethene

Propagating step

Terminating step

Or

Caprolactum and water at high temperature – Nylon 6 (correct equation) 2

1

1

1

1

A 6 carbon starting monomer

27 (i) essential amino acids

(ii) Glycogen

(iii) B

12

1

1

1

1

28 (i) Statement and explanation of Kohlrausch’s law

(ii) ΔG 0 = -nFE 0 cell

; substitution and correct answer 45548 KJm -1

Log kc = 𝑛𝐸

0 𝑐𝑒𝑙𝑙

; substitution and correct answer

0.059

Log kc = 8.00 k c

= 1x10 8

1+1

1 ½

1 ½

Or

(i) Fuel cell definition 1

Anode and cathode reactions ½ + ½

(ii) E cell

= E 0 cell

0.059

2 𝑙𝑜𝑔

[𝐹𝑒

2+

]

[𝐻 + ] 2

1

Oxidation reaction Fe Fe 2+ + 2e -

Reduction reaction 2H + + 2e - H

2

½ + ½

1 EMF calculation and correct answer 0.5185V

29. CH

3

Br+Mg CH

3

MgBr

O C O +CH

3

MgBr O = COMgBr

CH

3

O O

P/Cl

2

ClCH

2

C OH CH

3

C OH

H

2

O H

3

O +

NH

2

CH

2

COOH

O

A=CH

3

MgBr ; B=CH

3

C OMgBr

O

C=CH

3

C OH D= ClCH

2

C OH

E = NH

2

CH

2

COOH

OR

2 ½

2 ½

Kolbe’s electrolysis

[O]

C

5

H

10

O C

3

H

6

O

2

C ½

Arrival of formula by positive 2,4 DNP test and negative iodoform and Tollen’s test.

CH

3

CH

2

COCH

2

CH

3

[O] CH

3

CH

2

COOH

CH

3

CH

2

COONa Kolbe’s electrolysis CH

3

CH

2

CH

2

CH

3

A - CH

3

CH

2

COCH

2

CH

3

B - CH

3

CH

2

COOH C - CH

3

CH

2

CH

2

CH

3

1

1

1

1 1/2

30. A=Sulphur

C=SO

2

(g)

B=H

2

S gas

D=SO

3

gas

Reactions are

MnO

4

+ 8H + +5e → Mn 2+ + 4H

2

O X 2

SO

2

+ 2H

2

O→ SO

4

2+4H + +2e X 5

2MnO

4

+5 SO

2

+2H

2

O → 2Mn 4 +5 SO

4

2+4H +

V

2

O

5

(S)

2SO

2(S)

+ O

2(S)

→ 2SO

3(g)

[OR] a) i)XeF

4

+PF

5

→ [XeF

3

] + [PF

6

] - ii)U+3 ClF

3

→ UF

6

+3ClF iii)Ca

3

P

2

+ 6H

2

O →3Ca(OH)

2

+2PH

3 b) c) i) Correct Structure ii)Correct Structure

2

3

3

1

1

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