A study is made of the kinetic salt effects upon the outer-sphere electron transfer reaction between hexacyanoferrate(I1) and 4-pyridinecarboxylatopentaamminecobalt(III~. The observed salts effects are analyzed, taking into account the possible association of the reactants with the ions of the suppo
Kinetics of the reaction between hexacyanoferrate(III) and thiosulphate ions. The initial reaction
β Scribed by K.E. Howlett; B.L. Wedzicha
- Publisher
- Elsevier Science
- Year
- 1976
- Tongue
- English
- Weight
- 500 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0020-1693
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β¦ Synopsis
The kinetics of the reaction between hexacyanoferrate(IIl) and thiosulphate in aqueous solution have been investigated spectrophotometrically. The rate equation contains several terms. Results on the first few percent of reaction only are analysed here. The total initial rate consists of an uncatalysed part, viz. -d[Fe (CN),&]ldt = 38[H+][S,O,"]' mol t-' min-' at 298" K together with components caused by catalysis by acetate and by cations. The mechanistic reasons for this are investigated and the uncatalysed path is shown to correspond in rate to the decomposition of thiosulphate.
π SIMILAR VOLUMES
The kinetics of the oxidation of S20:-by CIOz-have been studied in aqueous alkaline solution at 90Β°C using classical titrimetric methods to follow the course of the reaction. The reaction takes place according to the stoichiometry SzO: - + 2C10z-+ 20H-= 2S042-+ 2Cl-+ H 2 0 even in large SzO:excess.
## Abstract The kinetics of the reaction between Mg^2+^ and EriochromeβBlackβT (EBT) has been investigated in the pH range between 7.05 and 9.0, in the presence of 12% ethanol. The reaction is found to consist of two parallel paths, one involving the tervalent unprotonated ligand, and one its monop