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The kinetics of deprotonation from C-H bond of enolic p-chloroacetophenone and þ-methoxyacetophenone by DCDMH has been studied in aqueous acetic acid medium. The substate order is complex whereas rate is independent of the concentration of oxidant. The action of entropy (-ΔS#) indicates the presence of a symmetrical transition state in the slow process of rate-determining step. The analysis revealed the products of the reaction to be þ-chloro- and þ-methoxy phenyl glyoxals.
"Study of Reactions between þ-substituted acetophenones and 1,3-dichloro-5,5-dimethyl hydantoin ", International Journal of Science & Engineering Development Research (www.ijrti.org), ISSN:2455-2631, Vol.8, Issue 1, page no.256 - 259, January-2023, Available :http://www.ijrti.org/papers/IJRTI2301040.pdf
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2456-3315 | IMPACT FACTOR: 8.14 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.14 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator
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