enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Bond energy - Wikipedia

    en.wikipedia.org/wiki/Bond_energy

    The bond dissociation energy (enthalpy) [4] is also referred to as bond disruption energy, bond energy, bond strength, or binding energy (abbreviation: BDE, BE, or D). It is defined as the standard enthalpy change of the following fission: R—X → R + X. The BDE, denoted by Dº(R—X), is usually derived by the thermochemical equation,

  3. Standard enthalpy of reaction - Wikipedia

    en.wikipedia.org/wiki/Standard_enthalpy_of_reaction

    If the enthalpies for each step can be measured, then their sum gives the enthalpy of the overall single reaction. [11] Finally the reaction enthalpy may be estimated using bond energies for the bonds which are broken and formed in the reaction of interest. This method is only approximate, however, because a reported bond energy is only an ...

  4. Bell–Evans–Polanyi principle - Wikipedia

    en.wikipedia.org/wiki/Bell–Evans–Polanyi...

    The activation energy may be used to characterize the kinetic rate parameter of a given reaction through application of the Arrhenius equation. The Evans–Polanyi model assumes that the pre-exponential factor of the Arrhenius equation and the position of the transition state along the reaction coordinate are the same for all reactions ...

  5. Binding energy - Wikipedia

    en.wikipedia.org/wiki/Binding_energy

    Bond energies and bond-dissociation energies are typically in the range of a few eV per bond. The bond-dissociation energy of a carbon-carbon bond is about 3.6 eV. Molecular level: Electron binding energy; Ionization energy Electron binding energy, more commonly known as ionization energy, [3] is a measure of the energy required to free an ...

  6. Thermodynamic databases for pure substances - Wikipedia

    en.wikipedia.org/wiki/Thermodynamic_databases...

    It is very difficult to measure the absolute amount of any thermodynamic quantity involving the internal energy (e.g. enthalpy), since the internal energy of a substance can take many forms, each of which has its own typical temperature at which it begins to become important in thermodynamic reactions.

  7. Gibbs–Helmholtz equation - Wikipedia

    en.wikipedia.org/wiki/Gibbs–Helmholtz_equation

    This equation quickly enables the calculation of the Gibbs free energy change for a chemical reaction at any temperature T 2 with knowledge of just the standard Gibbs free energy change of formation and the standard enthalpy change of formation for the individual components. Also, using the reaction isotherm equation, [8] that is

  8. Bond-dissociation energy - Wikipedia

    en.wikipedia.org/wiki/Bond-dissociation_energy

    The term bond-dissociation energy is similar to the related notion of bond-dissociation enthalpy (or bond enthalpy), which is sometimes used interchangeably.However, some authors make the distinction that the bond-dissociation energy (D 0) refers to the enthalpy change at 0 K, while the term bond-dissociation enthalpy is used for the enthalpy change at 298 K (unambiguously denoted DH° 298).

  9. Transition state theory - Wikipedia

    en.wikipedia.org/wiki/Transition_state_theory

    At 298 K, a reaction with ΔG ‡ = 23 kcal/mol has a rate constant of k ≈ 8.4 × 10 −5 s −1 and a half life of t 1/2 ≈ 2.3 hours, figures that are often rounded to k ~ 10 −4 s −1 and t 1/2 ~ 2 h. Thus, a free energy of activation of this magnitude corresponds to a typical reaction that proceeds to completion overnight at room ...