(a) Identify the chiral molecule in the following pair:

(b) Write the structure of the product when chlorobenzene is treated with methyl chloride in the presence of sodium metal and dry ether.

(C) Write the structure of the alkene formed by dehydrohalogenation of 1-bromo-1-methylcyclohexane with alcoholic KOH.

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Q. Write the structure of the product when chlorobenzene is treated with methyl chloride in the presence of sodium metal and dry ether.

Q. Write the structure of the alkene formed by dehydrohalogenation of

1

-bromo-

1

-methylcyclohexane with alcoholic KOH.

What happes when

n - butyl chloride is treated with alcoholic KOH.

bromobenzene is treated with Mg in the presence of dry ether.

Chlorobenzene is subjected to hydrolysis.

Ethyl chloride is treated with aqueous KOH

methyl bromide is treated with sodium in the presence of dry ether.

methyl chloride is treated with KCN ?

Predict all the alkenes that would be formed by dehydrohalogenation of the following halides with sodium ethoxide in ethanol and identify the major alkene:

(i) 1-Bromo-1-methylcyclohexane

(ii) 2-Chloro-2-methylbutane

(iii) 2,2,3-Trimethyl-3-bromopentane.

Q. Name the organic product formed when chlorobenzene is treated with sodium in dry ether?

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