Sangam: A Confluence of Knowledge Streams

A study of the electronic effects of various substituents on the course of an aromatic cyclodehydration reaction vs. a Elbs-type reaction

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dc.contributor Chemistry
dc.contributor Vingiello, Frank A.
dc.creator Thornton, James Robert
dc.date 2014-03-14T21:23:42Z
dc.date 2014-03-14T21:23:42Z
dc.date 1963
dc.date 2009-12-23
dc.date 2009-12-23
dc.date 2009-12-23
dc.date.accessioned 2023-02-28T18:20:44Z
dc.date.available 2023-02-28T18:20:44Z
dc.identifier etd-12232009-020703
dc.identifier http://hdl.handle.net/10919/40478
dc.identifier http://scholar.lib.vt.edu/theses/available/etd-12232009-020703/
dc.identifier.uri http://localhost:8080/xmlui/handle/CUHPOERS/269639
dc.description The acld-oata17zed oyclodehydrat1on reaction of 2-benzylphenyl l-naphthyl ketone gives two products! 9-(1-naphthyl)anthracene, the expected product and in addition lO-phenyl-l,2-benzanthracene. This second product is the one expected it the ketone were subjected to the conditions of an .Elba reaction. The effect of substituents on the course of this reaction was investigated by synthesizing six 2-benzylphenyl 1- and 2-naphthyl ketones and subjecting each of them to the acid catalyzed reaction and to Elba reaction conditions. Of the six ketones, two had unsubstituted benzyl groups, two had 3'-methyl groups in the benzyl group and the remaining two had ,'-tr1fluoromethyl groups. The original finding was confirmed and the other ketones that cyoilzed by either treatment gave the expected products. When 2-(3'-methylbenzyl) 2-naphthl1 ketone was subjected to Elbs reaction conditions, 9-(2-naphthyl)anthraoene, the product of aromatic oyclodehydrat1on, was obtained. An explanation oft the unusual experimental results is suggested. The results of treat1ng the ketones w1th alumina and w1th l1qu1d hydrogen fluoride are reported.
dc.description Ph. D.
dc.format v, 100 leaves
dc.format BTD
dc.format application/pdf
dc.format application/pdf
dc.language en
dc.publisher Virginia Tech
dc.relation OCLC# 20276215
dc.relation LD5655.V856_1963.T467.pdf
dc.rights In Copyright
dc.rights http://rightsstatements.org/vocab/InC/1.0/
dc.subject LD5655.V856 1963.T467
dc.subject Aromatic compounds -- Reactivity -- Experiments
dc.subject Ketones -- Reactivity -- Experiments
dc.title A study of the electronic effects of various substituents on the course of an aromatic cyclodehydration reaction vs. a Elbs-type reaction
dc.type Dissertation
dc.type Text


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