The distance and orientation dependence of the heterogeneous electron-transfer reaction between ferrocytochrome c (Fe(2+)Cc) and a silver film over nanosphere (AgFON) electrode is examined in detail using electrochemical surface-enhanced resonance Raman spectroscopy (SERRS) as a molecularly specific and structurally sensitive probe. The distance between the Fe2+ redox center and the electrode surface is controlled by varying the chain length x of an intervening carboxylic acid terminated alkanethiol, HS(CH2)(x)COOH, self-assembled monolayer (SAM). The orientation of the heme in Fe(2+)Cc with respect to the AgFON/S(CK2)(x) COOH electrode surface is controlled by its binding motif. Electrostatic binding of Fe(2+)Cc to AgFON/S(CH2)(x)COOH yields a highly oriented redox system with the heme edge directed toward the electrode surface. The binding constants were determined to be K = 5.0 x 10(6) M-1 and 1.1 x 10(6) M-1, respectively, for the x = 5 and s = 10 SAMs. In contrast, covalent binding of Fe(2+)Cc yields a randomly oriented redox system with no preferred direction between the heme edge and the electrode surface. SERRS detected electrochemistry demonstrates that Fe(2+)Cc electrostatically bound to the x = 5 AgFON/S(CH2)(x)COOH surface exhibits reversible oxidation to ferricytochrome c, whereas Fe2+Ce electrostatically bound to the x = 10 surface exhibits irreversible oxidation. In comparison, Fe(2+)Cc covalently bound to the x = 5 and x = 10 surfaces both exhibit oxidation with an intermediate degree of reversibility. in addition to these primary results, the work presented here shows that AgFON/S(CH2)(x)COOH surfaces (1) are biocompatible - Fe(2+)Cc is observed in its native state and (2) are stable to supporting electrolyte changes spanning a wide range of ionic strength and pH thus enabling, for the first time, SERRS studies of these variables in a manner not accessible with either the widely used colloid or electrochemically roughened SERS-active surfaces.