Abstract:
The rates of alkaline hydrolysis of seven acyclic and bridgehead esters of p-nitrophenyl carboxylic acids have been kinetically found to vary inversely with the size of t...Show MoreMetadata
Abstract:
The rates of alkaline hydrolysis of seven acyclic and bridgehead esters of p-nitrophenyl carboxylic acids have been kinetically found to vary inversely with the size of the substituent R group. Computer assisted molecular modeling techniques were used to suggest a steric and electrostatic rationale for the effect of R group size upon the rate of hydrolysis.
Published in: 1992 14th Annual International Conference of the IEEE Engineering in Medicine and Biology Society
Date of Conference: 29 October 1992 - 01 November 1992
Date Added to IEEE Xplore: 02 May 2011
ISBN Information:
