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S(N)1 reaction is faster in...

`S_(N)1` reaction is faster in

A

`CH_(3) CH_(2) Cl`

B

C

`CH_(3)- overset(CH_(3)) overset(|) underset(CH_(3)) underset(|)( C) - Cl`

D

`CH_(3) - underset(CH_(3)) underset(|) underset(CH_(2))underset(|)(C )H - Cl`

Text Solution

Verified by Experts

The correct Answer is:
C
`S_(N^1)` mechanism proceeds through carbocation intermediate.
`CH_(3)-overset(CH_(3)) overset(|)underset(CH_(3))underset(|)(C )-Cl` provides stable carbocation intermediate because it has tertiary carbon
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