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Question : 15
Total: 26
Give reasons:
(a)n -Butyl bromide has higher boiling point than t-butyl bromide.
(b) Racemic mixture is optically inactive.
(c) The presence of nitro group( − NO 2 ) at o ∕ p positions increases the reactivity of haloarenes towards nucleophilic substitution reactions.
(a)
(b) Racemic mixture is optically inactive.
(c) The presence of nitro group
Solution:
(i) Larger surface area, higher van der Waals' forces, higher the boiling point.
(ii) Rotation due to one enantiomer is cancelled by another enantiomer.
(iii)− NO 2 acts as electron withdrawing group or − I effect.
(ii) Rotation due to one enantiomer is cancelled by another enantiomer.
(iii)
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