Methyl bromide undergoes hydrolysis with aq.NaOH by SN2 route because
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NaOH by SN2 route because - a) tertiary carbocation is well stabilised. b) Steric interactions are more. c) Back side attack is more favourable.
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methly not N Y.o formilam sn2
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jadaf n2o bxbx nah2
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