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The Van 't Hoff equation relates the change in the equilibrium constant, K eq, of a chemical reaction to the change in temperature, T, given the standard enthalpy change, Δ r H ⊖, for the process. The subscript r {\displaystyle r} means "reaction" and the superscript ⊖ {\displaystyle \ominus } means "standard".
Equilibrium constants are determined in order to quantify chemical equilibria.When an equilibrium constant K is expressed as a concentration quotient, = [] [] [] [] it is implied that the activity quotient is constant.
In coordination chemistry, a stability constant (also called formation constant or binding constant) is an equilibrium constant for the formation of a complex in solution. It is a measure of the strength of the interaction between the reagents that come together to form the complex. There are two main kinds of complex: compounds formed by the ...
The role of water in the association equilibrium is ignored as in all but the most concentrated solutions the activity of water is constant. K is defined here as an association constant, the reciprocal of an acid dissociation constant. Each activity term { } can be expressed as the product of a concentration [ ] and an activity coefficient γ ...
The Benesi–Hildebrand method is a mathematical approach used in physical chemistry for the determination of the equilibrium constant K and stoichiometry of non-bonding interactions. This method has been typically applied to reaction equilibria that form one-to-one complexes, such as charge-transfer complexes and host–guest molecular ...
In particular, equilibrium constants for species in aqueous solution are dependent on ionic strength, as the quotient of activity coefficients varies with the ionic strength of the solution. The values of the standard free energy change and of the equilibrium constant are temperature dependent.
The decrease in zero-point energy due to deuterium substitution will then be more important for R'–H than for R–H, and R'–D will be stabilized more than R–D, so that the equilibrium constant K D for R' + D–R ⇌ R'–D + R is greater than K H. This is summarized in the rule the heavier atom favors the stronger bond. [19]
The lowercase letters (e, s, a, b, l) are system constants describing the contribution of the aerosol phase to the sorption process. [5] The capital letters (E, S, A, B, L) are solute descriptors representing the complementary properties of the compounds. Specifically, L is the gas–liquid partition constant on n-hexadecane at 298 K;