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Question

Reactivity of alkyl halides towards SN1 nucleophilic substitution reaction is:


A

3o > 2o > 1o

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B

3o < 1o < 2o

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C

3o < 2o < 1o

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D

2o < 1o < 3o

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Solution

The correct option is A

3o > 2o > 1o


Reactivity of alkyl halides towards SN1 nucleophilic substitution reaction is 3o > 2o > 1o because in SN1 nucleophilic reaction , the first and the slow step is the formation of a carbocation. Tertiary carbocation is more stable than a secondary carbocation which is more stable than a primary carbocation. Greater the stability of the carbocation, greater will be the ease of formation of carbocation, and hence faster will be the rate of the reaction.


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