MECHANISM OF PENTACHLOROETHANE DEHYDROCHLORINATION TO TETRACHLOROETHYLENE

Roberts, AL; Gschwend, PM

HERO ID

3559576

Reference Type

Journal Article

Year

1991

HERO ID 3559576
In Press No
Year 1991
Title MECHANISM OF PENTACHLOROETHANE DEHYDROCHLORINATION TO TETRACHLOROETHYLENE
Authors Roberts, AL; Gschwend, PM
Journal Environmental Science & Technology
Volume 25
Issue 1
Page Numbers 76-86
Abstract The dehydrochlorination of pentachloroethane to tetrachloroethylene was investigated to gain insight into mechanisms of hexachloroethane reduction as well as structure-reactivity relationships for polyhalogenated alkanes. Although the absence of deuterium exchange excludes the possibility of an (E1CB)R mechanism, several factors suggest the transition state possesses considerable carbanion character: the reaction is insensitive to buffer catalysis, exhibits a moderately large solvent kinetic isotope effect, and only displays a neutral mechanism at low pH. Though our results cannot rule out a stepwise (E1CB)I or (E1CB)ip sequence, we believe CHCl2CCl3 reacts via a concerted mechanism based on a comparison of its dehydrohalogenation kinetics with proton-exchange rates for CHCl3 and CHCl2CF3. Pentachloroethane reported in the reduction of hexachloroethane to tetrachloroethylene is unlikely to result from carbanion protonation. Rather, it may be diagnostic of free-radical reduction mechanisms. Because pentachloroethane reacts relatively rapidly, future studies of hexachloroethane reduction should consider whether pentachloroethane represents a reaction intermediate instead of dismissing it as a minor side product.
Wosid WOS:A1991EP99100011
Is Certified Translation No
Dupe Override No
Is Public Yes