Mechanism of oxidation of aromatic amines by peroxomonosulphate – a kinetic study
✍ Scribed by Maddy Satyanarayan Reddy; K. C. Rajanna; Ahmed Naseeruddin
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 369 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
Abstract
Oxidation of aromatic amines (substrate) by peroxomonosulphate (PMS) in phthalate buffers at various temperatures revealed first‐order dependence on [PMS] as well as [Substrate]. Rate of oxidation was found to increase with an increase in pH as well as dielectric constant (D) of the medium. The most plausible mechanism involving PMS^−^ and substrate in rate limiting step was proposed. Hammett's plot of log‐rate constant versus σ deviated from linearity. Deviations were explained due to para resonance interaction energies. © 1995 John Wiley & Sons, Inc.
📜 SIMILAR VOLUMES
The kinetics of the oxidation of aliphatic aldehydes, formaldehyde, acetaldehyde, propionaldehyde, n-butyraldehyde, and trichloroacetaldehyde by Peroxomonosulphate (PMS) was carried out in aqueous perchloric acid medium (0.1-1 M H+) a t constant ionic strength of 1.2 M in the temperature range 1O"-6
## Abstract Kinetics of oxidation of indole‐3‐acetic acid (IAA) by peroxomonosulphate (PMS) in aqueous acetonitrile medium has been investigated. The reaction follows a total second order, first order each with respect to [IAA] and [PMS]. The rate of the reaction was not affected by added [H^+^]. V
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The kinetics of oxidation of the aliphatic primary amines, n-propylarnine, n-butylarnine, and isoarnylarnine, by sodium N-brornobenzenesulfonarnide or bromamine-B (BAB) in sodium hydroxide medium has been studied at 35" C The reaction rate shows a First-order dependence each on [ BABl and [amine]. a