The measurement of stress relaxation in concentrated solutions of polymethyl methacrylate has revealed a relation between the spectrum of relaxation times, the weight average molecular weight, and the molecular weight distribution. The spectrum of relaxation times and the essentially identical theories developed by Rouse, Bueche, and Zimm are used to calculate an average relaxation time which is directly proportional to the weight average molecular weight. It is then shown that a first approximation to the distribution of molecular weights may be calculated if one assumes that the friction factor increases with the 1.5 power of the molecular weight. This distribution for selected samples of polymethyl methacrylate is compared with the Schulz distribution in which the parameters were obtained from light scattering and osmotic pressure experiments. The ratios Mz/Mw calculated from the theory and stress relaxation data on a rough fraction, a whole polymer, and a blend of two whole polymers are found to be 1.3, 1.7, and 1.9, respectively.