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  2. 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).

  3. Bond energy - Wikipedia

    en.wikipedia.org/wiki/Bond_energy

    The bond energy for H 2 O is the average energy required to break each of the two O–H bonds in sequence: Although the two bonds are the equivalent in the original symmetric molecule, the bond-dissociation energy of an oxygen–hydrogen bond varies slightly depending on whether or not there is another hydrogen atom bonded to the oxygen atom.

  4. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    The bond is labeled as "the strongest in organic chemistry," [1] because fluorine forms the strongest single bond to carbon. Carbon–fluorine bonds can have a bond dissociation energy (BDE) of up to 130 kcal/mol. [2] The BDE (strength of the bond) of C–F is higher than other carbon–halogen and carbon–hydrogen bonds.

  5. Homolysis (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Homolysis_(chemistry)

    Bond dissociation energy is determined by multiple factors: [4] The bond dissociation energy depends on the electronegativity of the species bonded. Electronegativity. Less electronegative atoms are better stabilizers of radicals, meaning that a bond between two electronegative atoms will have a higher BDE than a similar molecule with two less ...

  6. Binding energy - Wikipedia

    en.wikipedia.org/wiki/Binding_energy

    Bond energy and bond-dissociation energy are measures of the binding energy between the atoms in a chemical bond. It is the energy required to disassemble a molecule into its constituent atoms. This energy appears as chemical energy , such as that released in chemical explosions , the burning of chemical fuel and biological processes.

  7. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    The σ from the 2p is more non-bonding due to mixing, and same with the 2s σ. This also causes a large jump in energy in the 2p σ* orbital. The bond order of diatomic nitrogen is three, and it is a diamagnetic molecule. [12] The bond order for dinitrogen (1σ g 2 1σ u 2 2σ g 2 2σ u 2 1π u 4 3σ g 2) is three because two electrons are now ...

  8. Bond cleavage - Wikipedia

    en.wikipedia.org/wiki/Bond_cleavage

    The bond-dissociation energy of a bond is the amount of energy required to cleave the bond homolytically. This enthalpy change is one measure of bond strength . The triplet excitation energy of a sigma bond is the energy required for homolytic dissociation, but the actual excitation energy may be higher than the bond-dissociation energy due to ...

  9. Dissociation (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Dissociation_(chemistry)

    For instance, when an acid dissolves in water, a covalent bond between an electronegative atom and a hydrogen atom is broken by heterolytic fission, which gives a proton (H +) and a negative ion. Dissociation is the opposite of association or recombination.