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`S_(N)1` reaction is faster inA. `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(|)underset(|)(CH)-Cl` |
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Answer» Correct Answer - 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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