The kinetics of oxidation of the aliphatic primary amines, n-propylamine, n-butylamine, and isoamylamine, by N-sodio-N-bromobenznesulfonamide or bromamine-B (BAB), in the presence of osmium(VIII), has been studied in alkaline medium at 35ะC. In the presence of the catalyst, the experimental rate law
Kinetic and mechanistic study of oxidation of diethylamine by N-sodio-N-bromobenzene sulphonamide (Bromamine-B) in acid solution: Catalyzed by Ru(III)
โ Scribed by S. Ananda; Ravi J. D. Saldanha; K. M. L. Rai; B. M. Venkatesha
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 159 KB
- Volume
- 31
- Category
- Article
- ISSN
- 0538-8066
No coin nor oath required. For personal study only.
โฆ Synopsis
Kinetics of oxidation of diethylamine (DEA) by Bromamine-B (BAB) has been investigated at in acid solution with Ru(III) as catalyst. The oxidation behavior obeys 303 K the rate law, rate ฯญ k [BAB] [DEA] [Ru(III)] [H ฯฉ ] ฯชx where 'x' is less than unity indicating retardation of rate by [H ฯฉ ].
Added halide ions, the reaction product benzenesulphonamide, variation of ionic strength and dielectric constant of the medium do not have any significant effect on the rate. The protonation constant of monobromamine-B evaluated for the reaction is 32.3 at Activation parameters have been evaluated from Arrhenius plot. A mechanism 303 K. consistent with experimental results has been proposed.
๐ SIMILAR VOLUMES
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
The kinetics of oxidation of Norfloxacin [1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(lpiperazinyl)-3-quinoline carboxylic acid] by chloramine-B and N-chlorobenzotriazole has been studied in aqueous acetic acid medium (25% v/v) in the presence of perchloric acid at 323 K. For both the oxidants, the reacti
Manganese(III) solutions were prepared by known electrochemical methods in sulfuric acid, acetic acid, and pyrophosphate media. The nature of the oxidizing species present in manganese(III) solutions was characterized by spectrophotometric and redox potential measurements. Kinetics of oxidation of L