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General instructions :
Section A: Q.No 1 to 10 carry 1 mark each.
Section B: Q.No 1 1 to 15 carry 2 mark each.
Section A: Q.No 16 to 20 carry 1 mark each.
Section A: Q.No 21 carrIes 5 mark .
SECTION :A
MULTIBLE CHOICE QUESTIONS:
1. n-propyl alcohol and isopropyl alcohol can be chemically distinguished by which reagent:
a).PCl5
b).Reduction
c).Oxidation with potassium dichromate
d).Ozonolysis
7. Assertion :: Phenol forms 2, 4, 6 – tribromophenol on treatment with Br2 in carbon disulphide at 273K.
Reason : Bromine polarises in carbon disulphide.
9. Assertion : : Bond angle in ethers is slightly less than the tetrahedral angle.
Reason : : There is a repulsion between the two bulky (—R) groups.
SECTION:B
11. Write the most effective reagent used for the conversion of the following
a)prop 2-enol to prop 2-enal.
b)Prop 2-enal to prop 2-enol .
12. Write the conversion of the following reactions:
(i) Phenol to Benzene
(ii) Dehydration of propan-2-ol to propene
(iii) Friedel – Crafts acetylation of anisole
13. State the products of the following reactions:
SECTION:C
16. Give reason for the following
a)Explain why Lewis acid is not required in bromination of phenol?
b)The carbon-oxygen bond in phenol is slightly stronger than that in methanol. Why?
SECTION-D
21. Answer the following
a)Why (CH3)3C—Br on reaction with sodium methoxide (Na+ _OCH3) gives alkene as the main product and
not an ether.
b)Explain the mechanism of acid catalysed hydration of an alkene to form corresponding alcohol.