[Solution from source] Diazotisation of aniline gives benzenediazonium chloride, the intermediate B. In the cold it couples with N,N-dimethylaniline at the activated para position, giving the coloured azo dye p-(dimethylamino)azobenzene. The –NH–NH– (hydrazo) compound has no N=N chromophore, so it would not be the coloured coupling product. Answer (1).