Alkyl Halides - Result Question 14

####14. The increasing order of reactivity of the following halides for the SN1 reaction is

(2017 Main)

I. CH3CH(Cl)CH2CH3

II. CH3CH2CH2Cl

III. pH3COC6H4CH2Cl

(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:

  1. (i) The rate of SN1 reaction depends only upon the concentration of the alkyl halide.

(ii) SN1 reaction proceeds through the formation of carbocation.

The reactivity is decided by ease of dissociation of alkyl halide.

RXR+XΘ

Higher the stability of R+(carbocation), higher would be the reactivity towards SN1 reaction.

pH3COC6H4CH2 is the most stable carbocation due to resonance and then CH3CHCH2CH3 (2 2 carbocation) while CH3CH2CH2(1) is least stable.

Thus, the correct increasing order of the reactivity of the given halides towards the SN1 reaction is

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