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(A) The reaction sequence is as follows:$1$. $p$-Toluidine reacts with acetic anhydride in the presence of pyridine to form $N$-(p-tolyl)acetamide (co

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$2$-bromo-$4$-methylaniline

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(A) The reaction sequence is as follows:$1$. $p$-Toluidine reacts with acetic anhydride in the presence of pyridine to form $N$-(p-tolyl)acetamide (compound $A$).$2$. Compound $A$ undergoes electrophilic aromatic substitution with $Br_2$ in $CH_3COOH$. The acetamido group $(-NHCOCH_3)$ is ortho/para directing. Since the para position is occupied by a methyl group,bromine enters the ortho position relative to the acetamido group to form $2$-bromo-$4$-methylacetanilide (compound $B$).$3$. Finally,acid-catalyzed hydrolysis $(H^{\oplus}/H_2O)$ of the acetamido group in compound $B$ yields $2$-bromo-$4$-methylaniline (compound $C$).

$C$ will be

Similar Questions

Identify the product $Y$ in the following reaction sequence:
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In the following compounds,the order of basicity is as follows:

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In the given reaction,what will be the product?

How many isomers of $C_4H_{11}N$ are tertiary amines?

$Br-CH_2-(CH_2)_2-CH_2-Br + CH_3NH_2 \to$ The product of the reaction is:

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