in halogen compound which compound undergoes SN1 reaction faster
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(I), i.e. 2-chloro-2-methylpropane, undergoes faster SN1 reaction than (II) i.e., 3-chloropentane. The alkyl halide (I) is 2° while (II) is 1°. 2° carbocation is more stable than 1° carbocation. Therefore, (I), 2-chloroheptane, undergoes faster SN1 reaction than (II), 1-chlorohexane.
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Answered by
1
Answer:
2-chloro-2-methylpropane, undergoes SN1 REACTION FASTER.
Explanation:
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