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  2. Standard enthalpy of formation - Wikipedia

    en.wikipedia.org/wiki/Standard_enthalpy_of_formation

    Δ latt H corresponds to U L in the text. The downward arrow "electron affinity" shows the negative quantity –EA F , since EA F is usually defined as positive. For ionic compounds, the standard enthalpy of formation is equivalent to the sum of several terms included in the Born–Haber cycle .

  3. 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.

  4. Standard enthalpy of reaction - Wikipedia

    en.wikipedia.org/wiki/Standard_enthalpy_of_reaction

    The hydrogenation of one mole of acetylene yields ethane as a product and is described by the equation C 2 H 2 (g) + 2 H 2 (g) → C 2 H 6 (g). Standard enthalpy of neutralization is the change in enthalpy that occurs when an acid and base undergo a neutralization reaction to form one mole of water.

  5. Helmholtz free energy - Wikipedia

    en.wikipedia.org/wiki/Helmholtz_free_energy

    F is the Helmholtz free energy (sometimes also called A, particularly in the field of chemistry) (SI: joules, CGS: ergs), U is the internal energy of the system (SI: joules, CGS: ergs), T is the absolute temperature of the surroundings, modelled as a heat bath, S is the entropy of the system (SI: joules per kelvin, CGS: ergs per kelvin).

  6. Delta potential - Wikipedia

    en.wikipedia.org/wiki/Delta_potential

    The delta potential is the potential = (), where δ(x) is the Dirac delta function. It is called a delta potential well if λ is negative, and a delta potential barrier if λ is positive. The delta has been defined to occur at the origin for simplicity; a shift in the delta function's argument does not change any of the following results.

  7. 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 ...

  8. Thermodynamic free energy - Wikipedia

    en.wikipedia.org/wiki/Thermodynamic_free_energy

    Historically, the term 'free energy' has been used for either quantity. In physics, free energy most often refers to the Helmholtz free energy, denoted by A (or F), while in chemistry, free energy most often refers to the Gibbs free energy. The values of the two free energies are usually quite similar and the intended free energy function is ...

  9. Enthalpy - Wikipedia

    en.wikipedia.org/wiki/Enthalpy

    Enthalpy (/ ˈ ɛ n θ əl p i / ⓘ) is the sum of a thermodynamic system's internal energy and the product of its pressure and volume. [1] It is a state function in thermodynamics used in many measurements in chemical, biological, and physical systems at a constant external pressure, which is conveniently provided by the large ambient atmosphere.