Alkyl Halides - Result Question 14
14. The increasing order of reactivity of the following halides for the $S _N 1$ reaction is
(2017 Main)
I. $CH _3 CH(Cl) CH _2 CH _3$
II. $CH _3 CH _2 CH _2 Cl$
III. $p-H _3 CO-C _6 H _4-CH _2 Cl$
(a) (III) $<$ (II) $<$ (I)
(b) (II) $<$ (I) $<$ (III)
(c) (I) $<$ (III) $<$ (II)
(d) (II) $<$ (III) $<$ (I)
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Answer:
Correct Answer: 14. (b)
Solution:
- (i) The rate of $S _N 1$ reaction depends only upon the concentration of the alkyl halide.
(ii) $S _N 1$ reaction proceeds through the formation of carbocation.
The reactivity is decided by ease of dissociation of alkyl halide.
$ R-X \rightleftharpoons R^{\oplus}+X^{\Theta} $
Higher the stability of $R^{+}$(carbocation), higher would be the reactivity towards $S _N 1$ reaction.
$p-H _3 CO-C _6 H _4-CH _2{ }^{\oplus}$ is the most stable carbocation due to resonance and then $CH _3 \stackrel{\oplus}{C}HCH _2 CH _3$ ( $2^{\circ}$ carbocation) while $CH _3 CH _2 \stackrel{\oplus}CH _2 (1^{\circ})$ is least stable.
Thus, the correct increasing order of the reactivity of the given halides towards the $S _N 1$ reaction is
BETA
