Question

1. Methyl bromide undergoes hydrolysis with aq. NaOH by Sn2 route because -
a) tertiary carbocation is well stabilised. b) Steric interactions are more.
c) Back side attack is more favourable. d) None of these.​

Answer 1

Explanation:

c is the answer.......

Answer 2

Answer:

(c) is your answer

Explanation:

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