Arrange the compounds in increasing order of rate of reaction towards nucleophilic substitution.
1. (iii) < (ii) < (i)
2. (ii) < (iii) < (iii)
3. (i) < (iii) < (ii)
4. (i) <(ii) < (iii)
nucleophilic substitution reaction and trence, enhances rate of reaction.
Compound (iii) has three electron withdrawing groups at ortho and para positions wrt
chlorine while compound (ii) has only one electron withdrawing group and there is no
electron withdrawing group in compound (i). So, the increasing order of rate of reaction
towards nucleophilic substitution is (i)) < (ii) < (iii).
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