Studies in diphenyl chemistry

Marler, Elizabeth Esther Jessie

(1930)

Marler, Elizabeth Esther Jessie (1930) Studies in diphenyl chemistry.

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Abstract

The nitration of haloge-no-benzenes. The formation of unsymmetrical dinitro-derivatives of symmetrical 4;4'-dihalogeno-diphenyls The nitration of 4-chloro 4--- flluoro-diphenyl- and of 4-bromo:4' -fluoro-diphenyl. Reasons for expecting that more- of the-2:38-dinitro-derivative than of the 2':3- compound would he formed. Details of the method of analysis 4-Chloro:4'-fluoro-diphenyl underwent 7-1-. 6% of 2 :38 dinitratdon and 28.4% of 2' :3-dinitration. 4-Bromot4'-fluoro-diphenyl underwent 85.8% of 2:3'- and 14.2% of 2' :3-d-initrat ion. Experimental details of the preparation of the mixed dihalogeno-diphenyls; Attempts to study the effect of 4-:4' -halogen substituents on further halogen substitution in the diphenyl molecule. Small amounts of a tribromo- and a tetrahromo-diphenyl have been isolated.

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This is a Accepted version
This version's date is: 1930
This item is not peer reviewed

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https://repository.royalholloway.ac.uk/items/b535936d-8a5c-4865-a634-b69b5bda94a9/1/

Item TypeThesis (Masters)
TitleStudies in diphenyl chemistry
AuthorsMarler, Elizabeth Esther Jessie
Uncontrolled KeywordsOrganic Chemistry; Pure Sciences; Chemistry; Diphenyl; Diphenyls; Diphenyls; Studies
Departments

Identifiers

ISBN978-1-339-61228-7

Deposited by () on 31-Jan-2017 in Royal Holloway Research Online.Last modified on 31-Jan-2017

Notes

Digitised in partnership with ProQuest, 2015-2016. Institution: University of London, Bedford College (United Kingdom).


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