“…Exceptions are compounds bearing large substituents in the vicinity of the electroactive center and ortho-substituted aromatic compounds, where individual, specific effects predominate. For correlations using LFERs the data were obtained mostly from the literature, but successful correlations have been obtained also for our 8 P. ZUMAN experimental data for reductions of aromatic aldehydes and ketones (67,68,72), semicarbazones (66), N-and O-substituted oximes (73), sydnones (58), and nitro compounds (74,75) as well as nitrosobenzenes (76,77), nitriles (69), sulfones (78), and sulfonamides (79).…”