Total 4 structural isomers are possible.
Organic Compounds Containing Nitrogen
Because arylhalides do not undergo nucleophilic substitution reaction with potassium phthalimide easily.
Schotten-Bauman reaction is a method to synthesize amides from amines and acid chlorides.
Diazonium salt containing aryl group directly linked to the nitrogen atom is most stable due to resonance stabilization.
Secondary amine react with nitrous acid to give N-Nitrosoamines.
Hydrolysis of propyl isocyanide (CH 3 CH 2 CH 2 NC) gives CH 3 CH 2 CH 2 NH 2 + HCOOH.
On treatment with NaNO 2 and HCl I(CH 3 CH 2 CH 2 NH 2 ) gives CH 3 CH 2 CH 2 OH which does not give iodoform test.
II (HCOOH) reduces Tollen’s reagent and Fehling’s solution.
H 3 PO 2 and H 2 O works as a reducing agent.
As A gives alcohol on treatment with nitrous acid thus it should be primary amine.
C 3 H 9 N has two possible structure with –NH 2 group.
As it gives isopropylmethylamine thus it should be isopropyl amine not n-propyl amine.
Among the given reagents only NaOH/ Br 2 converts -CONH 2 group to -NH 2 group.
This is known as Hofmann bromamide reaction.
CH 3 -CONH 2 + NaOH +Br 2 CH 3 NH 2 + NaBr + Na 2 CO 3 + H 2 O
Aryl amines react with nitrous acid to form diazonium salt.