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  2. Van 't Hoff equation - Wikipedia

    en.wikipedia.org/wiki/Van_'t_Hoff_equation

    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. When ⁠ B / C ⁠ < 1, C is the favored product, and the data on the Van 't Hoff plot will be in the negative region.

  3. Gibbs free energy - Wikipedia

    en.wikipedia.org/wiki/Gibbs_free_energy

    In thermodynamics, the Gibbs free energy (or Gibbs energy as the recommended name; symbol ) is a thermodynamic potential that can be used to calculate the maximum amount of work, other than pressure–volume work, that may be performed by a thermodynamically closed system at constant temperature and pressure.

  4. Transition state theory - Wikipedia

    en.wikipedia.org/wiki/Transition_state_theory

    In 1884, Jacobus van 't Hoff proposed the Van 't Hoff equation describing the temperature dependence of the equilibrium constant for a reversible reaction: ⁡ = where ΔU is the change in internal energy, K is the equilibrium constant of the reaction, R is the universal gas constant, and T is thermodynamic temperature.

  5. Gibbs–Helmholtz equation - Wikipedia

    en.wikipedia.org/wiki/Gibbs–Helmholtz_equation

    The definition of the Gibbs function is = + where H is the enthalpy defined by: = +. Taking differentials of each definition to find dH and dG, then using the fundamental thermodynamic relation (always true for reversible or irreversible processes): = where S is the entropy, V is volume, (minus sign due to reversibility, in which dU = 0: work other than pressure-volume may be done and is equal ...

  6. Equilibrium constant - Wikipedia

    en.wikipedia.org/wiki/Equilibrium_constant

    For a system undergoing a reversible reaction described by the general chemical equation + + + + a thermodynamic equilibrium constant, denoted by , is defined to be the value of the reaction quotient Q t when forward and reverse reactions occur at the same rate.

  7. Determination of equilibrium constants - Wikipedia

    en.wikipedia.org/wiki/Determination_of...

    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. = [] [] []

  8. Binding constant - Wikipedia

    en.wikipedia.org/wiki/Binding_constant

    The binding constant, or affinity constant/association constant, is a special case of the equilibrium constant K, [1] and is the inverse of the dissociation constant. [2] It is associated with the binding and unbinding reaction of receptor (R) and ligand (L) molecules, which is formalized as:

  9. Arrhenius equation - Wikipedia

    en.wikipedia.org/wiki/Arrhenius_equation

    In physical chemistry, the Arrhenius equation is a formula for the temperature dependence of reaction rates.The equation was proposed by Svante Arrhenius in 1889, based on the work of Dutch chemist Jacobus Henricus van 't Hoff who had noted in 1884 that the van 't Hoff equation for the temperature dependence of equilibrium constants suggests such a formula for the rates of both forward and ...