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dc.contributor.authorSo, Kwok-Hung.en_US
dc.date.accessioned2009-07-09T18:43:03Z
dc.date.available2009-07-09T18:43:03Z
dc.date.issued1978-07-09T18:43:03Z
dc.identifier.urihttp://hdl.handle.net/10464/2072
dc.description.abstractThe preparation of phenacyl and para-phenylphenacyl esters, the reactions of carboxylic acids, phenols, 2-nitropropane and alcohols with alkyl halides in the presence of fluoride anion are described. The reactions are thought to be accelerated by the formation of hydrogen bonds between the fluoride anion and the organic electron acceptor. The fluoride ,carboxylic acids, fluoride-phenols and fluoride-2-nitropropane are better reaction systems than the fluoride-alcohol. The source of the fluoride anion and the choice of solvents are also discussed.en_US
dc.language.isoengen_US
dc.publisherBrock Universityen_US
dc.subjectOrganic compounds--Synthesis.en_US
dc.subjectHydrogen bonding.en_US
dc.titleStrong hydrogen bonding in organic synthesisen_US
dc.typeElectronic Thesis or Dissertationen_US
dc.degree.nameM.Sc. Chemistryen_US
dc.degree.levelMastersen_US
dc.contributor.departmentDepartment of Chemistryen_US
dc.degree.disciplineFaculty of Mathematics and Scienceen_US


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