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When determining the stability constants for ternary complexes, M p A q B r it is common practice the fix the values for the corresponding binary complexes M p′ A q′ and M p′′ B q′′, at values which have been determined in separate experiments. Use of such constraints reduces the number of parameters to be determined, but may result ...
These experiments enable one to artificially "enter" the reaction at any point, as the initial concentrations of one experiment (the intercepting reaction) are chosen to map directly onto the anticipated concentrations at some intermediate time, t, in another (the parent reaction). One would expect the reaction progress, described by the rate ...
In such a case A is the kinetic product and is favoured under kinetic control and B is the thermodynamic product and is favoured under thermodynamic control. [ 1 ] [ 2 ] [ 3 ] The conditions of the reaction, such as temperature, pressure, or solvent, affect which reaction pathway may be favored: either the kinetically controlled or the ...
The kinetic data (Figure 1a) shows the change in mass and humidity as a function of time. From the kinetic results, the rate of water uptake and water diffusion coefficients can be determined. The equilibrium mass values at the end of each humidity step were used to calculate the sorption and desorption isotherms (Figure 1b).
In 1923, Peter Debye and Erich Hückel reported the first successful theory for the distribution of charges in ionic solutions. [7] The framework of linearized Debye–Hückel theory subsequently was applied to colloidal dispersions by S. Levine and G. P. Dube [8] [9] who found that charged colloidal particles should experience a strong medium-range repulsion and a weaker long-range attraction.
In chemistry, chemical stability is the thermodynamic stability of a chemical system, in particular a chemical compound or a polymer. [1] Colloquially, it may instead refer to kinetic persistence , the shelf-life of a metastable substance or system; that is, the timescale over which it begins to degrade.
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The ideal kinetic resolution is that in which only one enantiomer reacts, i.e. k R >>k S. The selectivity (s) of a kinetic resolution is related to the rate constants of the reaction of the R and S enantiomers, k R and k S respectively, by s=k R /k S, for k R >k S. This selectivity can also be referred to as the relative rates of reaction.