๐”– Bobbio Scriptorium
โœฆ   LIBER   โœฆ

Substituent effects and mechanism in the micellar hydrolysis of hydroxamic acids

โœ Scribed by Berndt, Donald C.; Utrapiromsuk, Nop; Conran, Douglas E.

Book ID
126052447
Publisher
American Chemical Society
Year
1984
Tongue
English
Weight
485 KB
Volume
49
Category
Article
ISSN
0022-3263

No coin nor oath required. For personal study only.

๐Ÿ“œ SIMILAR VOLUMES

Micellar hydrolysis of hydroxamic acids.
Micellar hydrolysis of hydroxamic acids. Michaelis-menten kinetics
โœ Donald C. Berndt; Jill E. Angus; Michael J. Wood; Richard F. Atkinson; Tanveer A ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 364 KB

Rates of reaction for the alkaline hydrolysis of various hydroxamic acids in the presence of cetyltrimethylammonium bromide have been determined. Empirical reaction orders of zero, one-half, and one were found for the hydroxamic acids depending upon reaction conditions and substrate structure. N-met

Substituent effects in the acid-catalyse
Substituent effects in the acid-catalysed hydrolysis of alkylphenylphosphinanilides
โœ Martin J.P. Harger; Andrew J. Macpherson; David Pickering ๐Ÿ“‚ Article ๐Ÿ“… 1975 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 128 KB

Haake and Tyssee' postulated a dissociative (Al or Al-like) mechanism for the acidcatalysed hydrolysis of diphenylphosphinanilides 1. They considered cleavage of theP-N bond in the protonated anilide to be well advanced in the transition state 2 and nucleophilic participation by water to be small. A