Draw the structure of majos
monchalo product in each of the
following reactions
oh hexane -socl2
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Answer:
CH
3
I will react faster in S
N
2 reaction than CH
3
Br. This is because I
−
is a better leaving group, owing to its greater size than Br
−
. As a result, it will leave at a faster rate in the presence of an incoming nucleophile.
(ii) CH
3
Cl will react faster in S
N
2 reaction than (CH
3
)
3
−Cl, as CH
3
−Cl is a primary halide whereas (CH
3
)
3
C−Cl is a tertiary halide. Primary halides undergo S
N
2 reactions faster
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