Abstract 2, 2'-Dinitrophenyl ether (I) is reduced at less negative potentials than 2, 2'- dinitrodiphenylamine (II); the respective mechanism of their reduction differ essentially.(I) is electrolytically reduced in a single wave with an uptake of eight electrons per molecule, giving rise to a bishydroxylamine intermediate which undergoes an intramolecular disproportionation. The resulting 2-nitroso-2'-amino-diphenyl ether undergoes a chemical ...