The compound $A$ with the following sequence of reactions gives benzoic acid.
$A$ $\xrightarrow{NaNO_2/HCl} B$ $\xrightarrow{KCN} C$ $\xrightarrow{H_3O^{+}} \text{benzoic acid}$
The compound $A$ is:

  • A
    Nitrobenzene
  • B
    Aniline
  • C
    Benzaldehyde
  • D
    Amides

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Which one of the following compounds undergoes bromination of its aromatic ring (electrophilic aromatic substitution) at the fastest rate?

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$A$. Phenyl methanamine
$B$. $N,N$-Dimethylaniline
$C$. $N$-Methylaniline
$D$. Benzenamine
Choose the correct order of basic nature of the above amines.

The chemical reaction shown in the image represents the reduction of a diazonium salt to an aromatic hydrocarbon. Identify the reagent typically used for this transformation.

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