1. Methyl bromide undergoes hydrolysis with aq. NaOH by SN2 route because
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a) tertiary carbocation is well stabilised. b) Steric interactions are more.
c) Back side attack is more favourable. d) None of these.
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Answered by
9
Answer:
c) back side attack is more favourable
Explanation:
is correct answer
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Answered by
9
Answer:
option c is the correct answer
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