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If the correction factor is greater than one, the reaction displays an asymmetric amplification, also known as a positive non-linear effect. Under the ML 2 model, a (+)-NLE infers a less reactive heterochiral catalyst. In this case, the equilibrium constant K also increases as the correction factor increases.
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 ...
where ln denotes the natural logarithm, is the thermodynamic equilibrium constant, and R is the ideal gas constant.This equation is exact at any one temperature and all pressures, derived from the requirement that the Gibbs free energy of reaction be stationary in a state of chemical equilibrium.
There are two main kinds of complex: compounds formed by the interaction of a metal ion with a ligand and supramolecular complexes, such as host–guest complexes and complexes of anions. The stability constant(s) provide(s) the information required to calculate the concentration(s) of the complex(es) in solution.
In thermodynamics, a critical point (or critical state) is the end point of a phase equilibrium curve. One example is the liquid–vapor critical point, the end point of the pressure–temperature curve that designates conditions under which a liquid and its vapor can coexist.
For most non-electrolytes dissolved in water, the van 't Hoff factor is essentially 1. For most ionic compounds dissolved in water, the van 't Hoff factor is equal to the number of discrete ions in a formula unit of the substance. This is true for ideal solutions only, as occasionally ion pairing occurs in solution. At a given instant a small ...
The polar sensitivity factor ρ* can be obtained by plotting the ratio of the measured reaction rates (k s) compared to the reference reaction versus the σ* values for the substituents. This plot will give a straight line with a slope equal to ρ*. Similar to the Hammett ρ value:
The compressibility factor is defined as = where p is the pressure of the gas, T is its temperature, and is its molar volume, all measured independently of one another. In the case of an ideal gas, the compressibility factor Z is equal to unity, and the familiar ideal gas law is recovered: