Ac voltammetry (ACV) is used to determine the chain length dependence of electron transfer kinetics between gold bead electrodes and ruthenium redox centers attached to the electrode surface via short alkanethiols. The pentaamminepyridine ruthenium redox centers are attached to pre-assembled monolayers of mercaptoalkanecarboxylic acids (HS(CH2)(m)COOH, m = 5, 7, 10). Equations for faradaic admittance of strongly adsorbed, non-interacting electroactive species are fitted to the experimental faradaic admittance data. Kinetic heterogeneity is suggested to be a probable reason for the apparent increase in the standard rate constant (k(s)) and decrease in the total coverage of redox centers (theta (total)) as the perturbation frequency increases. Because of the frequency dependence of k(s) and because of limitations in the correction for uncompensated resistance, faradaic admittance at a fixed phase angle of 70 degrees is chosen to compare k(s) for different chain lengths. The plot of 1n(k(s)) versus m (the number of methylene units) is linear with a slope of - 1.2 +/- 0.1 per CH2.