Abstract
Acylarylamino compounds having chloro or methoxyl group at meta-or para-position of benzene ring were oxidized with hydrogen peroxide in varied conditions. In the case of introduction of electron-attracting group, yields of nitro compounds were fairly good and at the same time, considerable amounts of the starting materials were recovered, while, in the case of electron-releasing group, yields of nitro compounds were poor and almost none of the starting materials was recovered. Reasonable explanations of these phenomena were discussed.