The oxidation kinetics of 2-butanol by alkaline hexacyanoferrate(III) catalyzed by sodium ruthenate has been studied spectrophotometrically. The initial rates method was used for kinetic analysis. The reaction rate shows a fractional-order in [hexacyanoferrate(III)] and [substrate] and a first-order
Kinetic study of ruthenium (VI)-catalyzed oxidation of 2-propanol by alkaline hexacyanoferrate (III)
✍ Scribed by A. E. Mucientes; F. J. Poblete; M. A. Rodríguez; F. Santiago
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 101 KB
- Volume
- 12
- Category
- Article
- ISSN
- 0894-3230
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✦ Synopsis
The kinetics of Ru(VI)-catalyzed oxidation of 2-propanol by hexacyanoferrate(III) was investigated in alkaline media using a spectrophotometric technique. The reaction shows first order in [Ru(VI)], a Michaelis-Menten-type dependence on [2-propanol], a fractional order in [Fe(CN) 3À 6 ] and a complicated variation on [OH À ]. A reaction mechanism which involves two active catalytic species is proposed. Each of these species forms an intermediate complex with the substrate. These complexes decompose slowly, producing ruthenium(IV) complexes, which are reoxidized by hexacyanoferrate(III) in subsequent steps. The theoretical rate law obtained is in complete agreement with all the experimental observations.
📜 SIMILAR VOLUMES
with respect to the catalyst concentration is first. The reaction mechanism supposes the formation of a complex between the substrate and the catalyst active form . Subsequently, the complex thus formed slowly decomposes in the rate determining step to give carbonium ions and ruthenium hydride, sinc
## Abstract The kinetics of Ruthenium (III) catalysed oxidation of L‐Valine by alkaline solution of hexacyanoferrate (III) were studied by following the rate of disappearance of Fe(CN)^3‐^. The reaction shows zero order dependence on hexacyanoferrate (III). First order on ruthenium (III). The first
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