Leaving group and solvent effects in the aminolysis of phosphinates in aprotic media - by Asàad N. Hajj

dc.contributor.authorHajj, As'ad N.
dc.contributor.departmentDepartment of Chemistry
dc.contributor.facultyFaculty of Arts and Sciences
dc.contributor.institutionAmerican University of Beirut
dc.date1984
dc.date.accessioned2012-06-13T06:38:52Z
dc.date.available2012-06-13T06:38:52Z
dc.date.issued1984
dc.descriptionThesis (M.S.)--American University of Beirut. Department of Chemistry, 1984.;"Advisor: Robert Cook, Associate Professor, Chemistry --- Members of Committee: Costas Issidorides, Professor ,Chemistry Grainne Moran, Assistant Professor, Chemistry."
dc.descriptionBibliography: leaves 51-52.
dc.description.abstractThe n-butylaminolysis of some substituted phenyl diphenyl-phosphinates at 40°C in acetonitrile has been investigated. The rate expression fits the equation: Rate = k₂ [Amine] [Ester] + k3 [Amine]² [Ester]. The k3 component is predominant over the k2 comp
dc.format.extent[xiii], 52 leaves cm.
dc.identifier.urihttp://hdl.handle.net/10938/3891
dc.language.isoen
dc.relation.ispartofTheses, Dissertations, and Projects
dc.subject.classificationT:003194 AUBNO
dc.subject.lcshPhosphinates.
dc.titleLeaving group and solvent effects in the aminolysis of phosphinates in aprotic media - by Asàad N. Hajj
dc.typeThesis

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