We can conceive of a stepwise version of the SN2 reaction consisting of a Lawis acid-base dissociation
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We can conceive of a stepwise version of the SN2 reaction consisting of a Lawis acid-base dissociation followed by a Lewis acid-base association. (Nuc:- = a nucleophile.)
(a) Why should the stepwise process be slower than the concerted process?
(b) For what type of alkyl halide is the stepwise process likely to be observed?
Transcribed Image Text:
CH3 : :I: Nuc-CH3 Nuc: CH, Nuc:
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a The stepwise process involves formation of a methyl cat...View the full answer
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