Isotope effect on the location of variational transition states: The hydrogen exchange reaction

1986 ◽  
Vol 18 (9) ◽  
pp. 1079-1086
Author(s):  
Luis Bañares Morcillo ◽  
Angel Gonzalez Ureña ◽  
Michael Menzinger
1979 ◽  
Vol 57 (22) ◽  
pp. 2896-2901 ◽  
Author(s):  
Robert A. McClelland ◽  
William F. Reynolds

Rate constants have been obtained for the acid-catalyzed N–H exchange of N-methyl, 2,N-dimethyl, and 2,4,6,N-tetramethylbenzamide and the acid-catalyzed isomerization of the three corresponding N,N-dimethylbenzamides. The ratio [Formula: see text] increases significantly with increased number of ortho methyl substituents. This is explained in terms of a suggestion of Perrin, that C—N bond rotation is not completely free in the N-protonated amide, since it must compete with a diffusion limited deprotonation reaction. The isomerization reaction, which requires such a rotation, is therefore slowed by ortho methyl substituents which hinder rotation, relative to the exchange reaction, which does not require rotation.


2000 ◽  
Vol 323 (5-6) ◽  
pp. 586-593 ◽  
Author(s):  
Michio Okada ◽  
Kousuke Moritani ◽  
Mamiko Nakamura ◽  
Toshio Kasai ◽  
Yoshitada Murata

2001 ◽  
Vol 105 (29) ◽  
pp. 7079-7084 ◽  
Author(s):  
N. B. Okulik ◽  
R. Pis Diez ◽  
A. H. Jubert ◽  
P. M. Esteves ◽  
C. J. A. Mota

Sign in / Sign up

Export Citation Format

Share Document