Capon, Brian, Page, Michael I. and Sankey, G.H. (1972) The kinetics and mechanism of the hydrolysis of 2,3-(phenylmethylenedioxy)benzoic acid (OO?-benzylidene-2,3-dihydroxybenzoic acid). Journal of the Chemical Society, Perkin Transactions 2 (5). pp. 529-532. ISSN 1472-779X
Metadata only available from this repository.Abstract
The hydrolysis of OO-benzylidene-2,3-dihydroxybenzoic acid is considerably faster than that of OO-benzylidene-3,4-dihydroxybenzoic acid and OO-benzylidenecatechol. The pH-rate profile is of the form: kobs=k1/(1 +Ka/10–pH). The high rate is associated with the k1-term which probably arises from intramolecular general-acid catalysis. This kinetic parameters of this reaction are compared with those for the formally analogous inter-molecularly general-acid catalysed hydrolysis of benzylidenecatechol. OO-Benzylidene-2,3-dihydroxybenzoic acid is not intramolecularly hydrogen bonded in dilute solutions in carbon tetrachloride
Item Type: | Article |
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Subjects: | Q Science > Q Science (General) Q Science > QD Chemistry |
Schools: | School of Applied Sciences |
Related URLs: | |
Depositing User: | Sharon Beastall |
Date Deposited: | 12 Nov 2009 08:51 |
Last Modified: | 28 Aug 2021 10:52 |
URI: | http://eprints.hud.ac.uk/id/eprint/6196 |
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