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  2. Ice rules - Wikipedia

    en.wikipedia.org/wiki/Ice_rules

    In 1935, Linus Pauling used the ice rules to calculate the residual entropy (zero temperature entropy) of ice I h. [3] For this (and other) reasons the rules are sometimes mis-attributed and referred to as "Pauling's ice rules" (not to be confused with Pauling's rules for ionic crystals). A nice figure of the resulting structure can be found in ...

  3. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The bond energy is significantly weaker than those of Cl 2 or Br 2 molecules and similar to the easily cleaved oxygen–oxygen bonds of peroxides or nitrogen–nitrogen bonds of hydrazines. [8] The covalent radius of fluorine of about 71 picometers found in F 2 molecules is significantly larger than that in other compounds because of this weak ...

  4. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    [21] [22] Conversely, bonds to other atoms are very strong because of fluorine's high electronegativity. Unreactive substances like powdered steel, glass fragments, and asbestos fibers react quickly with cold fluorine gas; wood and water spontaneously combust under a fluorine jet. [5] [23]

  5. Dioxygen difluoride - Wikipedia

    en.wikipedia.org/wiki/Dioxygen_difluoride

    The O−O bond length is within 2 pm of the 120.7 pm distance for the O=O double bond in the dioxygen molecule, O 2 . Several bonding systems have been proposed to explain this, including an O−O triple bond with O−F single bonds destabilised and lengthened by repulsion between the lone pairs on the fluorine atoms and the π orbitals of the ...

  6. 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 ...

  7. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    Perfluoroalkanes are very stable because of the strength of the carbon–fluorine 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. Tetrahedral molecular geometry - Wikipedia

    en.wikipedia.org/wiki/Tetrahedral_molecular_geometry

    In the gas phase, a single water molecule has an oxygen atom surrounded by two hydrogens and two lone pairs, and the H 2 O geometry is simply described as bent without considering the nonbonding lone pairs. [citation needed] However, in liquid water or in ice, the lone pairs form hydrogen bonds with neighboring water molecules. The most common ...

  9. Fluoride - Wikipedia

    en.wikipedia.org/wiki/Fluoride

    Water and food sources of fluoride include community water fluoridation, seafood, tea, and gelatin. [ 52 ] Soluble fluoride salts, of which sodium fluoride is the most common, are toxic, and have resulted in both accidental and self-inflicted deaths from acute poisoning . [ 4 ]