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Nitration of some derivatives of vanillic and veratric acids

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dc.contributor.authorChew, Steven
dc.date.accessioned2011-03-16T22:31:36Z
dc.date.accessioned2022-10-25T05:38:49Z
dc.date.available2011-03-16T22:31:36Z
dc.date.available2022-10-25T05:38:49Z
dc.date.copyright1981
dc.date.issued1981
dc.description.abstractThe behaviour of methyl 4 - acetoxy - 3 - methoxybenzoate and methyl 3,4 - dimethoxybenzoate with nitric acid have been examined and compared. With methyl 4 - acetoxy - 3 - methoxybenzoate, only the 2 - nitro product was observed while with methyl 3,4 - dimethoxybenzoate, the 6 - nitro product was isolated. This has been rationalised by invoking a co-ordination mechanism. The effect of the nitration medium was also studied. Studies of the nitration of some methyl esters of vanillic acid in which the 4 - hydroxyl group had been esterified with various acyl groups have also been carried out, and again, the products of nitration in the 2 - position were found to predominate.en_NZ
dc.formatpdfen_NZ
dc.identifier.urihttps://ir.wgtn.ac.nz/handle/123456789/23315
dc.languageen_NZ
dc.language.isoen_NZ
dc.publisherTe Herenga Waka—Victoria University of Wellingtonen_NZ
dc.subjectVanillic acid
dc.subjectVeratric acid
dc.subjectNitration
dc.subjectChemistry
dc.titleNitration of some derivatives of vanillic and veratric acidsen_NZ
dc.typeTexten_NZ
thesis.degree.disciplineChemistryen_NZ
thesis.degree.grantorTe Herenga Waka—Victoria University of Wellingtonen_NZ
thesis.degree.levelMastersen_NZ
thesis.degree.nameMaster of Scienceen_NZ
vuwschema.type.vuwAwarded Research Masters Thesisen_NZ

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