The changes in molecular weights, their distributions, and initial rates have been measured, for a series of polystyrenes prepared by thermal and anionic procedures. The information obtained and previous results can be explained to a very large extent by a kinetic chain decomposition comprised of competing end and random initiation, depropagation, intra-and intermolecular transfer and termination by combination.Key words: Anioni c polysl yre ne; molec ular weight distributions; molecular weights; thermal poly· s t yre :1 e; polymer ; pc ! ys t y !"e~e de g!"2da t!op. ; pyrolys is; thermolys is.