𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Pressure and pH dependence of the kinetics of decarboxylative dechlorination of N-chloro-l-alanine

✍ Scribed by Michael C. Brown; Jason M. Lepree; Kenneth A. Connors


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
402 KB
Volume
28
Category
Article
ISSN
0538-8066

No coin nor oath required. For personal study only.

✦ Synopsis


The kinetics of decarboxylative dechlorination of N-chloroalanine were studied at 25" in aqueous HCI solutions covering the pH range 1.4 to 2.8. These data were compared with literature results, and were interpreted in terms of first-order reactions of the cationic, uncharged, and anionic forms of the reactant Pressure effect studies on the reaction of the anionic species yielded a volume of activation estimate of + 50 ? 3 cm3 mol-'. This result is consistent with a concerted fragmentation process.


πŸ“œ SIMILAR VOLUMES


Radiation-induced dechlorination of carb
✍ M. G. Katz; G. Baruch; L. A. Rajbenbach πŸ“‚ Article πŸ“… 1976 πŸ› John Wiley and Sons 🌐 English βš– 300 KB πŸ‘ 1 views

## Abstract The kinetics of the gamma‐radiation induced free‐radical chain reaction in solutions of carbon tetrachloride in __n__‐hexane (RH) was investigated in the temperature range of 297.5–373Β°K. Trichloromethyl radicals were produced by the reaction of radiolytically generated hexyl radicals w

Radiation-induced dechlorination of carb
✍ M. G. Katz; G. Baruch; L. A. Rajbenbach πŸ“‚ Article πŸ“… 1978 πŸ› John Wiley and Sons 🌐 English βš– 276 KB πŸ‘ 1 views

The kinetics of gamma-radiation-induced free-radical chain reactions in solutions of carbon tetrachloride in mixtures of varying composition of cyclohexane and n-hexane was investigated in the temperature range of 296"-413"K. Trichloromethyl radicals were produced by the reaction of radiolytically g

Kinetics of dehydrohalogenation of N-chl
✍ M. Elkhatib; L. Peyrot; J. P. Scharff; H. Delalu πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 199 KB πŸ‘ 1 views

The formation of 3-azabicyclo [3,3,0]oct-2-ene in the course of the synthesis of 3,0]octane using the Raschig process results from the following two consecutive reactions: chlorine transfer between the monochloramine and the 3-azabicyclo[3,3,0]octane followed by a dehydrohalogenation of the substitu