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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]
Assume two products B and C form in a reaction: a A + d D → b B, a A + d D → c C. In this case, K eq can be defined as ratio of B to C rather than the equilibrium constant. When B / C > 1, B is the favored product, and the data on the Van 't Hoff plot will be in the positive region.
A ligand C is chosen which forms a weaker complex with A The stability constant, K AC, is small enough to be determined by a direct method. For example, in the case of EDTA complexes A is a metal ion and C may be a polyamine such as diethylenetriamine .
In chemistry, biochemistry, and pharmacology, a dissociation constant (K D) is a specific type of equilibrium constant that measures the propensity of a larger object to separate (dissociate) reversibly into smaller components, as when a complex falls apart into its component molecules, or when a salt splits up into its component ions.
The affinity constants, k + and k −, of the 1879 paper can now be recognised as rate constants. The equilibrium constant, K, was derived by setting the rates of forward and backward reactions to be equal. This also meant that the chemical affinities for the forward and backward reactions are equal. The resultant expression
The concentrations of reactants and products in an equilibrium mixture are determined by the analytical concentrations of the reagents (A and B or C and D) and the equilibrium constant, K. The magnitude of the equilibrium constant depends on the Gibbs free energy change for the reaction. [2] So, when the free energy change is large (more than ...
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 ...
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 ...