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  2. Bond energy - Wikipedia

    en.wikipedia.org/wiki/Bond_energy

    The strength of a bond can be estimated by comparing the atomic radii of the atoms that form the bond to the length of bond itself. For example, the atomic radius of boron is estimated at 85 pm, [10] while the length of the B–B bond in B 2 Cl 4 is 175 pm. [11] Dividing the length of this bond by the sum of each boron atom's radius gives a ratio of

  3. Hydrogen bond - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_bond

    The strength of the bond to each of those atoms is equal. It is an example of a three-center four-electron bond. This type of bond is much stronger than a "normal" hydrogen bond. The effective bond order is 0.5, so its strength is comparable to a covalent bond.

  4. 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).

  5. Hydrofluoric acid - Wikipedia

    en.wikipedia.org/wiki/Hydrofluoric_acid

    This is in part a result of the strength of the hydrogen–fluorine bond, but also of other factors such as the tendency of HF, H 2 O, and F − anions to form clusters. [19] At high concentrations, HF molecules undergo homoassociation to form polyatomic ions (such as bifluoride, HF − 2) and protons, thus greatly increasing the acidity. [20]

  6. Valence bond theory - Wikipedia

    en.wikipedia.org/wiki/Valence_bond_theory

    Hybridization also explains the equal C-H bond strengths. [11] In an HF molecule the covalent bond is formed by the overlap of the 1s orbital of H and the 2p z orbital of F, each containing an unpaired electron. Mutual sharing of electrons between H and F results in a covalent bond in HF.

  7. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    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. For example, the BDEs of the C–X bond within a CH 3 –X molecule is 115, 104.9, 83.7, 72.1, and 57.6 kcal/mol for X = fluorine, hydrogen ...

  8. Molecular orbital theory - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_theory

    Electrons in non-bonding orbitals tend to be associated with atomic orbitals that do not interact positively or negatively with one another, and electrons in these orbitals neither contribute to nor detract from bond strength. [16] Molecular orbitals are further divided according to the types of atomic orbitals they are formed from. Chemical ...

  9. Bifluoride - Wikipedia

    en.wikipedia.org/wiki/Bifluoride

    The bifluoride ion has a linear, centrosymmetric structure (D ∞h symmetry), with an F−H bond length of 114 pm. [1] The bond strength is estimated to be greater than 155 kJ/mol. [2] In molecular orbital theory, the atoms are modeled to be held together by a 3-center 4-electron bond (symmetrical hydrogen bond), [3] in a sort of hybrid between a hydrogen bond and a covalent bond.