Kinetics of the transesterification reaction between phenyl carbanilate and 1 -octanol

Sutherland, Cathleen

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dc.contributor.author	Sutherland, Cathleen
dc.contributor.other	Youngstown State University, degree granting institution.
dc.contributor.other	Youngstown State University. Department of Chemistry.
dc.date.accessioned	2020-08-04T20:46:25Z
dc.date.available	2020-08-04T20:46:25Z
dc.date.issued	1973
dc.identifier.other	907407014
dc.identifier.other	b1678833
dc.identifier.uri	https://jupiter.ysu.edu/record=b1678833
dc.identifier.uri	http://hdl.handle.net/1989/15643
dc.description	iv, 50 leaves : illustrations ; 29 cm Thesis M.S. Youngstown State University 1973. Includes bibliographical references (leaves 49-50).	en_US
dc.description.abstract	The kinetics of the transesterification reaction between phenyl carbanilate and 1-octanol were studied. The reaction was carried out in 1, 2-dimethoxy ethane as the solvent at a temperature of 100°. Two mechanisms for the transesterification were possible; a two-step mechanism involving dissociation to isocyanate or a bimolecular displacement involving a carbonyl addition intermediate. The rate constants for both the above mechanisms were calculated from the experimental data. Neither of the above mechanisms alone could account for the experimental data and a dual mechanism was postulated.	en_US
dc.description.sponsorship	Youngstown State University. Department of Chemistry.	en_US
dc.language.iso	en_US	en_US
dc.publisher	[Youngstown, Ohio] : Youngstown State University, 1973.	en_US
dc.relation.ispartofseries	Master's Theses;no. 0051
dc.subject	Transesterification.	en_US
dc.subject	Chemical kinetics.	en_US
dc.subject	Octyl alcohol.	en_US
dc.title	Kinetics of the transesterification reaction between phenyl carbanilate and 1 -octanol	en_US
dc.type	Thesis	en_US

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