Which would undergo `S_(N^(2))` reaction faster in the following pair and why? `CH_(3)-CH_(2)-Br and CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))

Question

Which would undergo `S_(N^(2))` reaction faster in the following pair and why? `CH_(3)-CH_(2)-Br and CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))

Which would undergo `S_(N^(2))` reaction faster in the following pair and why?
`CH_(3)-CH_(2)-Br and CH_(3)-underset(CH_(3))underset(|)overset(CH_(3))overset(|)(C)-Br`.

Monjur Alahi

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2025-01-04 04:42

1 Answers

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Salim Ahmed Kawsar · Accepted Answer · 2023-02-05T15:29:48+06:00

Salim Ahmed Kawsar

`CH_(3)-CH_(2)-Br` because it is a primary alkyl halide and offers less steric hindrance to the attacking nucleophile as compared to the other alkyl halide which is of tertiary nature.

8 views Answered 2023-02-05 15:29