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  2. Lewis structure - Wikipedia

    en.wikipedia.org/wiki/Lewis_structure

    Lewis structure of a water molecule. Lewis structures – also called Lewis dot formulas, Lewis dot structures, electron dot structures, or Lewis electron dot structures (LEDs) – are diagrams that show the bonding between atoms of a molecule, as well as the lone pairs of electrons that may exist in the molecule.

  3. Carbon tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrafluoride

    Tetrafluoromethane is the product when any carbon compound, including carbon itself, is burned in an atmosphere of fluorine. With hydrocarbons, hydrogen fluoride is a coproduct. It was first reported in 1926. [7] It can also be prepared by the fluorination of carbon dioxide, carbon monoxide or phosgene with sulfur tetrafluoride.

  4. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Silicon tetrafluoride, similar to carbon tetrafluoride and germanium tetrafluoride, adopts a molecular tetrahedral structure. [81] SiF 4 is stable against heating or electric spark, but reacts with water (even moist air), metals, and alkalis, thus demonstrating weak acidic character. [82]

  5. 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 ...

  6. Carbonyl fluoride - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_fluoride

    Carbonyl fluoride can also be prepared by reaction of phosgene with hydrogen fluoride and the fluorination of carbon monoxide, although the latter tends to result in over-fluorination to carbon tetrafluoride. The fluorination of carbon monoxide with silver difluoride is convenient: CO + 2 AgF 2 → COF 2 + 2 AgF. Carbonyl fluoride is unstable ...

  7. Three-center four-electron bond - Wikipedia

    en.wikipedia.org/wiki/Three-center_four-electron...

    The 3-center 4-electron (3c–4e) bond is a model used to explain bonding in certain hypervalent molecules such as tetratomic and hexatomic interhalogen compounds, sulfur tetrafluoride, the xenon fluorides, and the bifluoride ion.

  8. Tetrafluoroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroethylene

    Tetrafluoroethylene is a synthetic colorless, odorless gas that is insoluble in water. Like all unsaturated fluorocarbons, it is susceptible to nucleophilic attack. It is unstable towards decomposition to carbon and carbon tetrafluoride (CF 4) and prone to form explosive peroxides in contact with air. [3] [4]

  9. Tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroborate

    The structure of the tetrafluoroborate anion, BF − 4. Tetrafluoroborate is the anion BF − 4. This tetrahedral species is isoelectronic with tetrafluoroberyllate (BeF 2− 4), tetrafluoromethane (CF 4), and tetrafluoroammonium (NF + 4) and is valence isoelectronic with many stable and important species including the perchlorate anion, ClO −