The redox characteristics of three series namely 5‐phenylmethylene‐2‐phenylhydrazonothiazolidin‐4‐ones, 3‐phenyl‐8‐oxobenzylidenthiazoles‐(2,3‐c)triazoles and ethyl‐2‐phenylhydrazono‐2‐benzimidazol‐2‐ylacetate has been investigated in nonaqueous acetonitrile, 1,2‐dichloroethane, tetrahydrofuran and dimethylsulfoxide at platinium and gold electrodes. Through controlled potential electrolysis, the oxidation and reduction products of each class of compounds can be separated and identified. The redox mechanism is suggested and proved.