Kinetics of the formation of substituted diamides of carbonic acid ...

A serious drawback which hindered the elucidation of many reaction mechanisms in organic chemistry, was the lack of accurate quantitative data. The classical investigation by Lapworth or the halogenation of ketones initiated a new kinetic era in organic chemistry promoting the search for more exact...

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Main Author: Smythe, LE
Format: Thesis
Language:unknown
Published: University Of Tasmania 2023
Subjects:
Online Access:https://dx.doi.org/10.25959/23246144
https://figshare.utas.edu.au/articles/thesis/Kinetics_of_the_formation_of_substituted_diamides_of_carbonic_acid/23246144
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spelling ftdatacite:10.25959/23246144 2023-06-11T04:10:55+02:00 Kinetics of the formation of substituted diamides of carbonic acid ... Smythe, LE 2023 https://dx.doi.org/10.25959/23246144 https://figshare.utas.edu.au/articles/thesis/Kinetics_of_the_formation_of_substituted_diamides_of_carbonic_acid/23246144 unknown University Of Tasmania In Copyright http://rightsstatements.org/vocab/InC/1.0/ article-journal Text ScholarlyArticle Thesis 2023 ftdatacite https://doi.org/10.25959/23246144 2023-06-01T12:13:39Z A serious drawback which hindered the elucidation of many reaction mechanisms in organic chemistry, was the lack of accurate quantitative data. The classical investigation by Lapworth or the halogenation of ketones initiated a new kinetic era in organic chemistry promoting the search for more exact knowledge of reaction mechanisms and the energy considerations involved. The reaction between urea and formaldehyde first occupied the attention or chemists some sixty years ago with the studies of Holzer, Ludy, Hemmelmayr, Goldschmidt, Einhorn, Hamburger and others. The greater portion of the work published since then related to the preparative aspects of the reaction and it was not until 1928 that the first serious attempt to suggest a reaction mechanism was made. ... Thesis Carbonic acid DataCite Metadata Store (German National Library of Science and Technology)
institution Open Polar
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op_collection_id ftdatacite
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description A serious drawback which hindered the elucidation of many reaction mechanisms in organic chemistry, was the lack of accurate quantitative data. The classical investigation by Lapworth or the halogenation of ketones initiated a new kinetic era in organic chemistry promoting the search for more exact knowledge of reaction mechanisms and the energy considerations involved. The reaction between urea and formaldehyde first occupied the attention or chemists some sixty years ago with the studies of Holzer, Ludy, Hemmelmayr, Goldschmidt, Einhorn, Hamburger and others. The greater portion of the work published since then related to the preparative aspects of the reaction and it was not until 1928 that the first serious attempt to suggest a reaction mechanism was made. ...
format Thesis
author Smythe, LE
spellingShingle Smythe, LE
Kinetics of the formation of substituted diamides of carbonic acid ...
author_facet Smythe, LE
author_sort Smythe, LE
title Kinetics of the formation of substituted diamides of carbonic acid ...
title_short Kinetics of the formation of substituted diamides of carbonic acid ...
title_full Kinetics of the formation of substituted diamides of carbonic acid ...
title_fullStr Kinetics of the formation of substituted diamides of carbonic acid ...
title_full_unstemmed Kinetics of the formation of substituted diamides of carbonic acid ...
title_sort kinetics of the formation of substituted diamides of carbonic acid ...
publisher University Of Tasmania
publishDate 2023
url https://dx.doi.org/10.25959/23246144
https://figshare.utas.edu.au/articles/thesis/Kinetics_of_the_formation_of_substituted_diamides_of_carbonic_acid/23246144
genre Carbonic acid
genre_facet Carbonic acid
op_rights In Copyright
http://rightsstatements.org/vocab/InC/1.0/
op_doi https://doi.org/10.25959/23246144
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