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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. For example, the formation of lithium fluoride,

  3. Enthalpy of neutralization - Wikipedia

    en.wikipedia.org/wiki/Enthalpy_of_neutralization

    In chemistry and thermodynamics, the enthalpy of neutralization (ΔH n) is the change in enthalpy that occurs when one equivalent of an acid and a base undergo a neutralization reaction to form water and a salt. It is a special case of the enthalpy of reaction. It is defined as the energy released with the formation of 1 mole of water.

  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. Gibbs free energy - Wikipedia

    en.wikipedia.org/wiki/Gibbs_free_energy

    The reaction C (s) diamond → C (s) graphite has a negative change in Gibbs free energy and is therefore thermodynamically favorable at 25 °C and 1 atm. However, the reaction is too slow to be observed, because of its very high activation energy. Whether a reaction is thermodynamically favorable does not determine its rate.

  6. 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 ...

  7. Spontaneous process - Wikipedia

    en.wikipedia.org/wiki/Spontaneous_process

    positive, the process is non-spontaneous as written, but it may proceed spontaneously in the reverse direction. zero, the process is at equilibrium, with no net change taking place over time. This set of rules can be used to determine four distinct cases by examining the signs of the Δ S and Δ H .

  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. Hess's law - Wikipedia

    en.wikipedia.org/wiki/Hess's_law

    A representation of Hess's law (where H represents enthalpy) Hess's law of constant heat summation, also known simply as Hess's law, is a relationship in physical chemistry and thermodynamics [1] named after Germain Hess, a Swiss-born Russian chemist and physician who published it in 1840.