The shape of integral intensity of the depolarized component of Rayleigh light scattering on molecules of pivalic acid has been analyzed in the temperature range covering partly plastic and liquid phase. The occurrence of fast reorientations of pivalic acid monomers, earlier searched for by other authors, has been confirmed. This kind of motion was observed only in the liquid phase. The motion in the plastic phase is, as earlier established, a slow reorientation which involves breaking up of the double hydrogen bonds joining two adjacent molecules of pivalic acid and formation of a new bond with one of the twelve closest neighbours. The decay constant of the pure interaction-induced processes in the liquid and plastic phase as well as the squares of the effective anisotropy of the optical polarizability and anisotropy due to the pure interaction-induced processes were determined. A comparative analysis of integral intensity of the depolarized components at the transition from the plastic to the liquid phase, was performed for pivalic acid and succinonitrile.