For the solvolysis of Co(4-t-Bupy)rClz-ions in water + methanol and water + ethanol, log (rate constant) does not vary linearly with the reciprocal of the dielectric constant. The Gibbs free energy, the enthalpy, and the entropy of activation are insensitive to changes in the solvent composition in
Kinetics of the solvolysis oftrans-dichlorotetra-(4-t-butylpyridine)-cobalt(III) ions in water +t-butyl alcohol mixtures
โ Scribed by Kamal H. M. Halawani; Cecil F. Wells
- Publisher
- Springer US
- Year
- 1990
- Tongue
- English
- Weight
- 561 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0095-9782
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๐ SIMILAR VOLUMES
The kinetics of the solvolysis of the ion trans-[Coen2N3C11' have been investigated a t several temperatures in mixtures of water with t-butyl alcohol with concentrations of the latter ranging up to 50 vol% or a mol fraction of 0.16. Values for the enthalpy and entropy of activation show sharp chang
The kinetics of the solvolysis of the hydrophobic ion, Co(4-t-Bupy)dCl:, have been followed in mixtures of water with co-solvents having a hydrophilic tendency, ethane-1,2-diol and 2-methoxyethanol. The variation of ln(rate constant) with the reciprocal of the dielectric constant is nonlinear for bo
## Abstract Rates of solvolysis of complex ions [Co(3Rpy)~4~Cl~2~]^+^ with R = __Me__ and __Et__ have been determined in mixtures of water with __t__โbutyl alcohol over a range of temperatures. Extrema found in the enthalpy ฮ__H__\* and entropy ฮ__S__\* of activation are correlated with the physica