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dc.contributor.authorAnderson, Williamen
dc.date.accessioned2018-01-31T11:15:37Z
dc.date.available2018-01-31T11:15:37Z
dc.date.issued1938en
dc.identifier.urihttp://hdl.handle.net/1842/26114
dc.description.abstracten
dc.description.abstractVarious bromonitro derivatives of acenaphthene, fluorene, and diphenyl have been prepared and the reactivities of the bromine atoms towards piperidine measured.en
dc.description.abstractWith the exception of those diphenyl derivatives in which the bromo and nitro groups occupied positions in different rings, the results are in accordance with Fuson's vinylogy theory.en
dc.description.abstractIn some instances the results have been used to shed light on the arrangement of double bonds in aromatic compounds.en
dc.description.abstractA comparison has also been made of the reactivities of the bromine atoms in the bromonitrobenzenes with those of the bromonitrotoluenes, the results indicating that the presence of another substituent in the ring modifies the halogen activity to a various extent depending on the position of the substituent.en
dc.description.abstractAn unsuccessful attempt to study the problem of the structure of naphthalene by another method has also been described.en
dc.publisherThe University of Edinburghen
dc.relation.isreferencedbyAlready catalogueden
dc.subjectAnnexe Thesis Digitisation Project 2017 Block 15en
dc.titleThe structures of aromatic polycyclic compoundsen
dc.typeThesis or Dissertationen
dc.type.qualificationlevelDoctoralen
dc.type.qualificationnamePhD Doctor of Philosophyen


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