Statement-I: Nucleophilc substitution reactions of methyl bromide proceed through SN2 mechanism preferablyStatement-II: Hydrolysis of methyl bromide gives a product with inversion in configuration.
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a
Both statements -I and II are correct
b
Statement-I is correct and statement -II is incorrect
c
Statement-I is incorrect and statement -II is correct
d
Both statements -I and II are Incorrect
answer is B.
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Detailed Solution
Due to least-steric hindrance, CH3Br undergoes alkaline hydrolysis through SN2 mechanism. The product formed is methanol which has no chirality, the phrase “inversion in configuration” has no meaning.