Answer to Question #157555 in Organic Chemistry for hussein

Question #157555

1.      Which of the following alkyl halides would you expect to undergo SN1 reaction most rapidly? 

A   CH3CH2CH2CH2CH2Br

B   CH3CH2CH2CH(CH3)Br

C   CH3CH2C(CH3)2Br

D   All of them reacts at the same rate.


1
Expert's answer
2021-01-22T06:25:11-0500

answer: C, because intermediate carbocation is the most stable out of the options


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