Question

in halogen compound which compound undergoes SN1 reaction faster
​

Answer 1

Answer:

(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.

Explanation:

Answer 2

Answer:

2-chloro-2-methylpropane, undergoes SN1 REACTION FASTER.

Explanation: