The major product in the following reaction s | vedclass

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(C) The reaction sequence is as follows:$1$. Toluene reacts with $Br_2$ in the presence of $UV$ light to undergo free-radical substitution at the benz

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($2$-bromoethyl)benzene

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(C) The reaction sequence is as follows:$1$. Toluene reacts with $Br_2$ in the presence of $UV$ light to undergo free-radical substitution at the benzylic position,forming benzyl bromide $(C_6H_5CH_2Br)$.$2$. Benzyl bromide reacts with $Mg$ in dry ether to form the Grignard reagent,benzylmagnesium bromide $(C_6H_5CH_2MgBr)$.$3$. The Grignard reagent reacts with formaldehyde $(CH_2O)$ followed by acidic hydrolysis $(H_3O^+)$ to form $2-$phenylethanol $(C_6H_5CH_2CH_2OH)$.$4$. Finally,$2$-phenylethanol reacts with $PBr_3$ to replace the hydroxyl group with a bromine atom,yielding ($2$-bromoethyl)benzene $(C_6H_5CH_2CH_2Br)$.

The major product in the following reaction sequence is:

Similar Questions

Which reagent cannot be used to prepare an alkyl halide from an alcohol?

Benzyl chloride $(C_6H_5CH_2Cl)$ is prepared from toluene by chlorination with ................?

Which among the following reactions does $NOT$ form alkyl halides?

The products $A$ and $B$ obtained in the following reactions,respectively,are
$3 ROH + PCl_3 \rightarrow 3 RCl + A$
$ROH + PCl_5 \rightarrow RCl + HCl + B$

Which among the following methods is $NOT$ suitable for the preparation of alkyl chlorides?

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