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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. Dehalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehalogenation

    The rate of dehalogenation depends on the strength of the bond between the carbon and halogen atom. The bond dissociation energies of carbon-halogen bonds are described as: H 3 C−I (234 kJ/mol), H 3 C−Br (293 kJ/mol), H 3 C−Cl (351 kJ/mol), and H 3 C−F (452 kJ/mol).

  4. Homolysis (chemistry) - Wikipedia

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

    Homolytic cleavage is driven by the ability of a molecule to absorb energy from light or heat, and the bond dissociation energy . If the radical species is better able to stabilize the radical, the energy of the SOMO will be lowered, as will the bond dissociation energy. Bond dissociation energy is determined by multiple factors: [4]

  5. Bond cleavage - Wikipedia

    en.wikipedia.org/wiki/Bond_cleavage

    In chemistry, bond cleavage, or bond fission, is the splitting of chemical bonds. This can be generally referred to as dissociation when a molecule is cleaved into two or more fragments. [1] In general, there are two classifications for bond cleavage: homolytic and heterolytic, depending on the nature of the process

  6. Bond energy - Wikipedia

    en.wikipedia.org/wiki/Bond_energy

    Bond energy (BE) is the average of all bond-dissociation energies of a single type of bond in a given molecule. [7] The bond-dissociation energies of several different bonds of the same type can vary even within a single molecule. For example, a water molecule is composed of two O–H bonds bonded as H–O–H.

  7. Organoiodine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organoiodine_chemistry

    This periodic order also follows the atomic radius of halogens and the length of the carbon-halogen bond. For example, in the molecules represented by CH 3 X, where X is a halide, the carbon-X bonds have strengths, or bond dissociation energies, of 115, 83.7, 72.1, and 57.6 kcal/mol for X = fluoride, chloride, bromide, and iodide, respectively. [2]

  8. Iodine compounds - Wikipedia

    en.wikipedia.org/wiki/Iodine_compounds

    The H–I bond dissociation energy is likewise the smallest of the hydrogen halides, at 295 kJ/mol. [5] Aqueous hydrogen iodide is known as hydroiodic acid , which is a strong acid. Hydrogen iodide is exceptionally soluble in water: one litre of water will dissolve 425 litres of hydrogen iodide, and the saturated solution has only four water ...

  9. Radical (chemistry) - Wikipedia

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

    The homolytic bond dissociation energies, usually abbreviated as "ΔH °" are a measure of bond strength. Splitting H 2 into 2 H •, for example, requires a ΔH ° of +435 kJ/mol, while splitting Cl 2 into two Cl • requires a ΔH ° of +243 kJ/mol. For weak bonds, homolysis can be induced thermally.