Cyclic voltammetry, impedance and chronocoulometry have been employed for a quantitative study of 2-methyl-2-butanol (tert-PenOH) adsorption at the bismuth single crystal plane I aqueous Na2SO4 solution interface. The adsorption characteristics of tert-PenOH, obtained from the impedance and chronocoulometry measurements, are in reasonable agreement within the limits of surface charge densities - 16 < a < 2 muC cm(-2). The adsorption characteristics (Gibbs energy of adsorption -DeltaG(A)degrees; limiting Gibbs adsorption Gamma (max); limiting potential shift of zero charge E-N; molecular interaction parameter a, etc.) of tert-PenOH depend on the crystallographic structure of the electrode surface. Comparison of the adsorption parameters for n-propanol (n-PrOH), n-butanol (n-BuOH), tert-butanol (tert-BuOH), tert-PenOH and n-hexanol (n-HexOH) shows that the adsorption activity and other parameters depend on the length and structure of the hydrocarbon radical of the organic compound studied. The adsorption activity of tert-PenOH increases in the order of Bi planes (001) < (111) < (011) as the interfacial density of the planes increases. The limiting Gibbs adsorption Gamma (max) and the molecular interaction parameter a decrease in the order of planes (001) greater than or equal to (111) > (011). Very low Gamma (max) and E-N values for the Bi(011) plane indicate that tert-PenOH molecules probably have a flat orientation on the chemically most active Bi(011) single crystal plane. Comparison of the adsorption characteristics for the Bi I tert-PenOH interface with the data for Au single crystal planes [8,9,12] and Hg [14,25] is given.