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Question
Arrange the following compounds in increasing order of rate of reaction towards nucleophilic substitution.
(a) | ![]() |
(b) | ![]() |
(c) | ![]() |
Options
(a) < (b) < (c)
(c) < (b) < (a)
(a) < (c) < (b)
(c) < (a) < (b)
Solution
(a) < (c) < (b)
Explanation:
The presence of an electron-withdrawing group (−NO2) at the ortho and para position facilitates nucleophilic substitution. The effect of the presence of the electron-withdrawing group is very less at the meta position.
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