Abstract
The alkaline hydrolysis of dicarboxylic esters have been studied in mixed solvent systems of dioxan-water and acetone-water. The two rate constants have been obtained by the Frost Schwemer method combined with the Laidler-Landskroner Transition state, the results are consistent with an ion dipole process for both steps. The results indicate that increasing distance between the carbethoxy groups leads to a limiting value for the ratio which for any given solvent composition range is not sensitive to specific influences.
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Based on the thesis of R.V.V. approved for the Ph.D. Degree of the Madras University, 1963.
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Anantakrishnan, S.V., Venkatarathnam, R.V. Kinetic studies in ester hydrolysis. Proc. Indian Acad. Sci. 65, 188–194 (1967). https://doi.org/10.1007/BF03049530
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DOI: https://doi.org/10.1007/BF03049530