Statement 1: Anilinium chloride is more acidic than ammonium chloride.Statement 2: Anilinium chloride is resonance stabilised.

Aniline is weaker base than ammonium chloride. In NH4CI or aliphatic amines, the non-bonding electron pair of N is localized and is fully available for coordination with a proton.C6H5NH3⊕(stronger acid)→C6H5NH2+H+(weaker-conjugate base)On the other hand, in aniline and other aromatic amines, the non-bonding electron pair is delocalised into benzene ring by resonance.But anilinium ion is less resonance stabilised than aniline