Allyl phenyl ether can be prepared by heating | vedclass

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Question

(B) is the correct option. Allyl phenyl ether is prepared by the $Williamson$ ether synthesis. In this reaction,sodium phenoxide $(C_6H_5-ONa)$ acts a

Vedclass · Accepted Answer

$CH_2=CH-CH_2-Br + C_6H_5-ONa$

Vedclass · Answer

(B) is the correct option. Allyl phenyl ether is prepared by the $Williamson$ ether synthesis. In this reaction,sodium phenoxide $(C_6H_5-ONa)$ acts as a nucleophile and attacks the electrophilic carbon of allyl bromide $(CH_2=CH-CH_2-Br)$ via an $S_N2$ mechanism. Aryl halides like bromobenzene $(C_6H_5-Br)$ do not undergo nucleophilic substitution under ordinary conditions due to the partial double bond character of the $C-X$ bond. Reaction: $C_6H_5-ONa + Br-CH_2-CH=CH_2 \rightarrow C_6H_5-O-CH_2-CH=CH_2 + NaBr$

Allyl phenyl ether can be prepared by heating:

Similar Questions

Give $IUPAC$ names of the following ethers:
$(i)$ $C_2H_5OCH_2CH(CH_3)_2$
$(ii)$ $CH_3OCH_2CH_2Cl$
$(iii)$ $O_2NC_6H_4OCH_3(p)$
$(iv)$ $CH_3CH_2CH_2OCH_3$
$(v)$ $1$-Ethoxy-$4,4$-dimethylcyclohexane
$(vi)$ Ethoxybenzene

Which of the following products is formed when ether is exposed to air?

Identify $Z$ in the sequence of reactions :
$CH_3CH_2CH=CH_2$ $\xrightarrow{HBr/H_2O_2} Y$ $\xrightarrow{C_2H_5ONa} Z$

The reaction of $CH_3-O-C_2H_5$ with $HI$ gives:

Find the major product in the given reaction:

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