The given compound CH_3-O-CH_2-Br undergoes w | vedclass

Name: Exam Paper Generator | JEE NEET Paper Generator | Vedclass
Brand: Vedclass
Rating: 5 (35 reviews)

Question

(C) $CH_3-O-CH_2-Br$ is a primary alkyl halide,which facilitates the $S_N2$ reaction pathway.Additionally,the carbocation intermediate $CH_3-O-CH_2^+$

Vedclass · Accepted Answer

$S_N1$ as well as $S_N2$

Vedclass · Answer

(C) $CH_3-O-CH_2-Br$ is a primary alkyl halide,which facilitates the $S_N2$ reaction pathway.Additionally,the carbocation intermediate $CH_3-O-CH_2^+$ is significantly stabilized by the resonance effect of the lone pair on the oxygen atom $(CH_3-O^+=CH_2)$.Due to this stabilization,the compound can also undergo $S_N1$ reactions.Therefore,the compound exhibits both $S_N1$ and $S_N2$ reaction mechanisms.

The given compound $CH_3-O-CH_2-Br$ undergoes which of the following reactions?

Similar Questions

Which of the following will react faster through the $S_N 1$ mechanism?

Pure $CHCl_3$ and pure $CHI_3$ can be distinguished by which of the following?

The reaction of $CH_3CD_2CHBr-CH_2CD_3$ with alc. $KOH$ yields:

Which of the following represents the $(R)$-enantiomer of $1$-chloro-$1$-deutero-$1$-($4$-chlorophenyl)methane?

Identify the product of the following reaction:
(See image for reaction scheme)
Product; The product is:

Vedclass Test Series

Exam Paper Generator

Online Exam Module