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The nitration of phenols in acetic acid

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dc.contributor.author Copping, Alice Mary
dc.date.accessioned 2011-12-13T21:27:07Z
dc.date.accessioned 2022-10-31T21:30:23Z
dc.date.available 2011-12-13T21:27:07Z
dc.date.available 2022-10-31T21:30:23Z
dc.date.copyright
dc.date.copyright 1926
dc.date.issued 1926
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/27103
dc.description.abstract It is remarkable to note how little attention has been paid to the study of nitration of aromatic compounds in the advance of organic research. The first papers of interest were those published by Martinsen (J.C.S. 1905, A (ii), 149 and 1907 A (ii), 169). He investigated the nitration of phenol in aqueous solution with increasing acid concentration and recognised the fact that the reaction was auto-catalysed by nitrous acid. Further, he accounted for the effect of substituents in the ring on the rate of nitration. Klemenc (J.C.S. 1919, A. 272) from studies of the nitration of phenol in ethereal solution concluded that the reaction was bimolecular. He found that nitric acid free from nitrous acid or nitrogen peroxide did not cause nitration, and that the rate of the reaction was dependent on the concentration of the nitrous acid. These results agreed with the observations of Brauner on the bromination of benzene in the presence of iodine. en_NZ
dc.format pdf en_NZ
dc.language en_NZ
dc.language.iso en_NZ
dc.publisher Te Herenga Waka—Victoria University of Wellington en_NZ
dc.title The nitration of phenols in acetic acid en_NZ
dc.type Text en_NZ
vuwschema.type.vuw Awarded Research Masters Thesis en_NZ
thesis.degree.grantor Te Herenga Waka—Victoria University of Wellington en_NZ
thesis.degree.level Masters en_NZ


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