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  2. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbonfluorine_bond

    Carbonfluorine bond. The carbonfluorine bond is a polar covalent bond between carbon and fluorine that is a component of all organofluorine compounds. It is one of the strongest single bonds in chemistry (after the B–F single bond, Si–F single bond, and H–F single bond), and relatively short, due to its partial ionic character.

  3. Bent's rule - Wikipedia

    en.wikipedia.org/wiki/Bent's_rule

    Because carbon is more electronegative than hydrogen, the electron density in a C-H bond will be shortened and the C-F bond will be elongated. The same trend also holds for the chlorinated analogs of methane, although the effect is less dramatic because chlorine is less electronegative than fluorine. [2]

  4. Electronegativity - Wikipedia

    en.wikipedia.org/wiki/Electronegativity

    For the Nightfall EP, see Electronegative (EP). Electrostatic potential map of a water molecule, where the oxygen atom has a more negative charge (red) than the positive (blue) hydrogen atoms. Electronegativity, symbolized as χ, is the tendency for an atom of a given chemical element to attract shared electrons (or electron density) when ...

  5. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    The carbonfluorine bond is usually very stable. Organofluorine compounds are widely used as refrigerants, electrical insulation, and PTFE (Teflon). Pharmaceuticals such as atorvastatin and fluoxetine contain C−F bonds. The fluoride ion from dissolved fluoride salts inhibits dental cavities and so finds use in toothpaste and water fluoridation.

  6. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Fluorine's chemistry is dominated by its strong tendency to gain an electron. It is the most electronegative element and elemental fluorine is a strong oxidant. The removal of an electron from a fluorine atom requires so much energy that no known reagents are known to oxidize fluorine to any positive oxidation state. [20]

  7. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    Perfluoroalkanes are very stable because of the strength of the carbonfluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...

  8. Molecular orbital diagram - Wikipedia

    en.wikipedia.org/wiki/Molecular_orbital_diagram

    A diatomic molecular orbital diagram is used to understand the bonding of a diatomic molecule. MO diagrams can be used to deduce magnetic properties of a molecule and how they change with ionization. They also give insight to the bond order of the molecule, how many bonds are shared between the two atoms.

  9. Octet rule - Wikipedia

    en.wikipedia.org/wiki/Octet_rule

    Octet rule. The bonding in carbon dioxide (CO 2): all atoms are surrounded by 8 electrons, fulfilling the octet rule. The octet rule is a chemical rule of thumb that reflects the theory that main-group elements tend to bond in such a way that each atom has eight electrons in its valence shell, giving it the same electronic configuration as a ...