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.

$\underset{(\mathrm{stronger} \mathrm{acid})}{{\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_3^{\oplus }}\to \underset{(\mathrm{weaker}-\mathrm{conjugate} \mathrm{base})}{{\mathrm{C}}_6{\mathrm{H}}_5{\mathrm{NH}}_2+{\mathrm{H}}^{+}}$

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