## Abstract The kinetics of oxidation of sulfanilic acid (SAA) by chloramineβB (CAB) and bromamineβB (BAB) has been investigated in alkaline medium at 35 Β± 0.1Β°C. The oxidation reaction follows identical kinetics in the case of both the oxidants with firstβorder dependence on each [oxidant]~o~ and
Kinetic, mechanistic and spectral studies for the oxidation of sulfanilic acid by alkaline hexacyanoferrate(III)
β Scribed by Sairabanu A. Farokhi; Sharanappa T. Nandibewoor
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- French
- Weight
- 292 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
The kinetics of oxidation of sulfanilic acid (p-aminobenzenesulfonic acid) by hexacyanoferrate(III) in alkaline medium was studied spectrophotometrically. The reaction showed first order kinetics in hexacyanoferrate(III) and alkali concentrations and an order of less than unity in sulfanilic acid concentration (SAA). The rate of reaction increases with increase in alkali concentration. Increasing ionic strength increases the rate but the dielectric constant of the medium has no significant effect on the rate of the reaction. A retarding effect was observed by one of the products i.e. hexacyanoferrate(II) (HCF(II)). A mechanism involving the formation of a complex between sulfanilic acid and hexacyanoferrate(III) has been proposed. The reaction constants involved in the mechanism are evaluated. There is a good agreement between the observed and calculated rate constants under different experimental conditions. Investigations at different temperatures allowed the determination of the activation parameters with respect to the slow step of the proposed mechanism.
π SIMILAR VOLUMES
## Abstract The kinetics of the Ru(VI)βcatalyzed oxidation of benzyl alcohol by hexacyanoferrate(III), in an alkaline medium, has been studied using a spectrophotometric technique. The initial rates method was used for the kinetic analysis. The reaction is first order in [Ru(VI)], while the order c
## Abstract The oxidation of halotoluenes by hexacyanoferrate(III) in aqueous acetic acid containing perchloric acid (0.5__M__) at 50Β°C gave the corresponding aldehyde as the major product, and a small amount of polymeric material. The order with respect to each of the reactantsβsubstrate, oxidant,