A radioactive tracer study of the photolysis of N-chloroacetamide

dc.contributor.author	Millar, Keith Raymond
dc.date.accessioned	2010-11-22T22:25:21Z
dc.date.accessioned	2022-10-24T23:41:08Z
dc.date.available	2010-11-22T22:25:21Z
dc.date.available	2022-10-24T23:41:08Z
dc.date.copyright	1958
dc.date.issued	1958
dc.identifier.uri	https://ir.wgtn.ac.nz/handle/123456789/22576
dc.description.abstract	The mechanism of the rearrangement of halogenoamines such as N-chloroacetanilide has been the subject of a vast volume of work ever since G. Bender Ber., 1886, 192, 2272. studied the displacement of the aminic hydrogen of acetanilide by chlorine. On the other hand, the photolysis of this type of compound has received little treatment, although the fact that they decompose in the presence of light is well known. The earlier investigations were confined to the conversion of N-chloroacetanilide into a mixture of o- and p-chloroacetanilides in the presence of hydrochloric acid.	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	A radioactive tracer study of the photolysis of N-chloroacetamide	en_NZ
dc.type	Text	en_NZ
vuwschema.type.vuw	Awarded Research Masters Thesis	en_NZ
thesis.degree.discipline	Chemistry	en_NZ
thesis.degree.grantor	Te Herenga Waka—Victoria University of Wellington	en_NZ
thesis.degree.level	Masters	en_NZ

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