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Some Chloro Nitro Derivatives of Metacresol: Colour and Constitution of Benzene Azophenols

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dc.contributor.author Mason, Ethelwyn Margaret
dc.date.accessioned 2011-12-13T21:27:49Z
dc.date.accessioned 2022-10-31T21:42:06Z
dc.date.available 2011-12-13T21:27:49Z
dc.date.available 2022-10-31T21:42:06Z
dc.date.copyright 1932
dc.date.issued 1932
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/27129
dc.description.abstract Although a considerable amount of work has been done on the chloro-nitro derivatives of metacresol, the series is not yet complete, and some confusion exists as to the identity of certain members. This is in some measure due to an alternative method of nomenclature adopted by the Americans, ho number from the hydroxyl group, instead of from the methyl group, so that with them, 6- chloro- 4- nitro-m-cresol (133°) becomes 4- chloro-6-nitro-m -cresol. Another factor causing incorrect orientation, is a tendency to displace halogen groups shown by entering nitro- groups. Robertson (T. 1912 1961) , showed that 6- chloro- thymol on nitration yielded 2- chloro-6-ni\tro thymol, as well as considerable quantities of 6-nitro- tbymol, and 2.6. dinitro- thymol. 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 Some Chloro Nitro Derivatives of Metacresol: Colour and Constitution of Benzene Azophenols 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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