Ultrathin gold films, with thicknesses between the onset of conductivity (d similar to 5 mn) and the electron mean free path (d similar to 80 nm), display surface-sensitive resistivities, which have been exploited to follow the adsorption and desorption of molecular monolayers at the metal-solution interface with high precision. For nominal Au film thicknesses (d similar to 40 nm), strongly chemisorbed thiolate monolayers increase the resistivity of the thin Au films by similar to 4%, but weakly adsorbed species, such as pyridine or phenolate at open circuit, induce no observable change in the Au film resistance. Resistivity measurements implemented with a high-stability current source and high precision digital voltmeter sampling at 1 Hz resulted in 3 sigma uncertainties in alkanethiolate coverage of 1.4 x 10(-4) monolayer, Surface plasmon resonance measurements, performed simultaneously with resistivity measurementsi indicate that changes in resistivity vary monotonically with coverage with three distinct regions: a low-coverage region of heightened adsorbate mobility, an intermediate-coverage region with generally linear behavior, and a chain length-dependent saturation region at high coverages. Resistivity measurements were also capable of reproducibly following the chemical state of the Au surface through a complex set of redox manipulations, demonstrating the versatility of this simple measurement.