Seyhan Ozturk Seyhan Ozturk, Shahin Shahabi Shahin Shahabi, Halil Kutuk Halil Kutuk
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引用次数: 0
Abstract
In this study, the mechanism of acid catalyzed hydrolysis of N-(4-substitutedaryl) succinimides in different acids was investigated. These acids are hydrochloric acid, perchloric acid and sulfuric acid, which were studied at 50.0and#177;0.1and#176;C. Analyses of the results obtained with the entropy of activation, Excess Acidity treatment and substituent effect are consistent across the entire acid studied by an A-2 mechanism. The catalytic order of strong acids for the acid catalyzed hydrolysis of the compounds studied were as HCl andgt; H2SO4 andgt; HClO4 in the whole range of acidity. This order is characteristics for an A–2 mechanism.
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This journal covers different research areas in the field of Chemistry. These include; Analytical Chemistry, Applied Chemistry, Biochemistry, Environmental Chemistry, Industrial Chemistry, Inorganic Chemistry, Organic Chemistry and Physical Chemistry. The journal publishes full length articles and Reviews from researchers in academia in addition to featuring comments. Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry.
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