Dibenzoylmesitylene undergoes protiodeacylation in 89.8% (w/w) sulfuric acid at ca. 9O"C, with subsequent sulfonation, to give mesitylenedisulfonic acid. The reaction involves a single-path sequence of four first-order reactions. The corresponding reaction of acetylbenzoylmesitylene can proceed by t
Kinetic analysis of an extended single-path sequence of first-order reactions. The reaction of mesitonitrile in sulfuric acid
✍ Scribed by Ja′far Al-ka′bi; Peter H. Gore; Esmat F. Saad; David N. Waters; Gerald F. Moxon
- Publisher
- John Wiley and Sons
- Year
- 1983
- Tongue
- English
- Weight
- 277 KB
- Volume
- 15
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
✦ Synopsis
The system of a sequence of five first-order reactions, A -B -C -D -E -F , has been analyzed kinetically. An actual example is proposed in the reaction of mesitonitrile in 89.8% (w/w) sulfuric acid a t 98.3OC. The analysis provides estimates of concentration ratios as functions of time, and the progress of the buildup and decay of the intermediate species can he monitored. The kinetics have been measured for the hydration of mesitonitrile, the hydrolysis of mesitamide, and the sulfonation of mesitylenesulfonic acid in 89.8% sulfuric acid. The calculated values of the concentration ratios of mesitylenedisulfonic acid as a function of time were satisfactorily close to those found in experiment.
📜 SIMILAR VOLUMES