Concept:
Important name reactions of aldehydes, amines and diazonium salts are recognized by their characteristic reagents and products.
Step 1: Identify the Cannizzaro reaction.
Benzaldehyde undergoes disproportionation in concentrated NaOH to form benzyl alcohol and sodium benzoate.
\[
2C_6H_5CHO + NaOH
\rightarrow
C_6H_5CH_2OH + C_6H_5COONa
\]
This is the
Cannizzaro reaction.
\[
(a)\rightarrow(q)
\]
Step 2: Identify the Carbylamine reaction.
Primary amines react with chloroform and alcoholic KOH to produce isocyanides.
\[
C_6H_5NH_2
\xrightarrow[alc.\,KOH]{CHCl_3}
C_6H_5NC
\]
This is the
Carbylamine reaction.
\[
(b)\rightarrow(s)
\]
Step 3: Identify the Gattermann reaction.
Diazonium salts react with Cu/HBr (or Cu/HCl) to form haloarenes.
\[
ArN_2^+Cl^-
\xrightarrow{Cu/HBr}
ArBr
\]
This is the
Gattermann reaction.
\[
(c)\rightarrow(p)
\]
Step 4: Identify the Sandmeyer reaction.
Diazonium salts react with cuprous salts such as CuCN to form substituted aromatic compounds.
\[
ArN_2^+Cl^-
\xrightarrow{CuCN}
ArCN
\]
This is the
Sandmeyer reaction.
\[
(d)\rightarrow(r)
\]
\[
\begin{aligned}
\text{Cannizzaro reaction} &: (q) \\
\text{Carbylamine reaction} &: (s) \\
\text{Gattermann reaction} &: (p) \\
\text{Sandmeyer reaction} &: (r)
\end{aligned}
\]
Therefore,
\[
(a-q),\quad (b-s),\quad (c-p),\quad (d-r)
\]
\[
\boxed{(a-q),\quad (b-s),\quad (c-p),\quad (d-r)}
\]
Hence, option \(\mathbf{(D)}\) is correct.