Chemistry, asked by gabc984, 10 months ago

which would undergo sn2 rxn faster and why
CH3-CH-CH2-CH2-Br
|
CH3.
AND
CH3-CH2-CH-CH2-Br
|
CH3

Answers

Answered by logeshwarar
0

Answer:

The second compound will undergo the sn2 rxn mechanism easily

Explanation:

because during the rear attack due to bulky alkyl group's steric hinderance may happen and nucleophile may not travel upto molecule in molecule 1 so the second molecule will undergo the sn2 rxn mechanism easily.

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