Step 1: Understanding the Concept
Diazotisation is the reaction of an amine with nitrous acid (\(\text{NaNO}_2+\text{HCl}\)) at 273-278 K to form a diazonium salt.
Step 2: Which amine
Primary aromatic amines such as aniline form arenediazonium salts, which are stable at low temperature because of resonance with the ring.
Step 3: Eliminate
Aliphatic primary amines give unstable diazonium salts that decompose to alcohols, and secondary amines give nitrosoamines.
Final Answer:
Aromatic primary amines undergo diazotisation.
\[ \boxed{\text{(B) }\text{Aromatic primary amine}} \]