We present the first scanning tunneling microscopy (STM) study of the rotational dynamics of organic species on any oxide surface. Specifically, variable-temperature STM and dispersion-corrected density functional theory (DFT-D) are used to study the alkyl chain conformational disorder and dynamics of 1-, 2-, 3- and 4-octoxy on rutile TiO2(110). Initially, the geminate pairs of the octoxy and bridging hydroxyl species are created via octanol dissociation on bridging-oxygen (O-b) vacancy defects. The STM images provide time-averaged snapshots of octoxy species rotating among multiple energetically nearly degenerate configurations accessible at a given temperature. In the calculations we find that the underlying corrugated potential energy surface is a result of the interplay between attractive van der Waals dispersion forces, leading to weak attractive C center dot center dot center dot Ti and repulsive C center dot center dot center dot O-b interactions which lead to large barriers of 50-70 kJ mol(-1) for the rotation of the octoxy alkyl chains across the O-b rows. In the presence of the geminate hydroxyl groups we find that the relative populations of the various conformations as well as the rotational barriers are perturbed by the presence of geminate hydroxyl due to additional C center dot center dot center dot hydroxyl repulsions.