“…However, the electrochemical reduction of nitro-aromatic compounds is complicated as a consequence of the various chemical transformations involved in the process, which are strongly dependent on pH, solvent and catalytic nature. [42][43][44][45] Nonetheless, in protic media, the predominant reduction product is either aminophenol and/or aniline, depending upon the strength of the acidic medium, [46][47][48] while in aprotic media it is 4-hydroxylaminophenol. For example, in an acidic electrolyte (10% H 2 SO 4 ), nitrophenol is reduced to aminophenol in a virtually quantitative yield.…”