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 compli
Kinetics and mechanism of the oxidation of butane-2,3-diol by alkaline hexacyanoferrate (III), catalyzed by ruthenium trichloride
✍ Scribed by A. Mucientes Balado; F. Santiago Jimenez; F. J. Poblete Martín; R. Varón Castellanos
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 143 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0538-8066
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✦ Synopsis
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, since ruthenium (III) abstracts a hydride ion from the ␣carbon atom of the diol .
In particular, the kinetics of oxidation of butane-2,3-diol has not been studied. In this article, we report the results of our experimental research on the
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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
## 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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