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  2. Hydrogen fluoride - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_fluoride

    Hydrogen fluoride (fluorane) is an inorganic compound with chemical formula H F. ... 1,1-Difluoroethane is produced by adding HF to acetylene using mercury as a catalyst.

  3. Hydrofluoric acid - Wikipedia

    en.wikipedia.org/wiki/Hydrofluoric_acid

    Hydrofluoric acid is a solution of hydrogen fluoride (HF) in water.Solutions of HF are colorless, acidic and highly corrosive.A common concentration is 49% (48-52%) but there are also stronger solutions (e.g. 70%) and pure HF has a boiling point near room temperature.

  4. Tetrachloro-1,2-difluoroethane - Wikipedia

    en.wikipedia.org/wiki/Tetrachloro-1,2-difluoroethane

    CFC-112 can be made in a reaction with hydrogen fluoride with hexachloroethane or tetrachloroethane with extra chlorine. This reaction occurs with an aluminium fluoride catalyst with some extra iron, nickel and chromium at 400°C. With the extra metal in the catalyst yield of the isomer can be 98% compared with the unsymmetrical isomer. [2]

  5. Fluoroantimonic acid - Wikipedia

    en.wikipedia.org/wiki/Fluoroantimonic_acid

    Fluoroantimonic acid is a mixture of hydrogen fluoride and antimony penta­fluoride, containing various cations and anions (the simplest being H 2 F + and SbF − 6).This mixture is a superacid stronger than pure sulfuric acid, by many orders of magnitude, according to its Hammett acidity function.

  6. Linear alkylbenzene - Wikipedia

    en.wikipedia.org/wiki/Linear_alkylbenzene

    Hydrogen fluoride (HF) and aluminium chloride (AlCl 3) are the two major catalysts for the alkylation of benzene with linear mono-olefins. The HF-based process is commercially dominant; however, the risk of releasing HF (a poisonous substance) into the environment became a concern particularly after the Clean Air Act Amendment.

  7. Fluorination with aminosulfuranes - Wikipedia

    en.wikipedia.org/wiki/Fluorination_with_amino...

    Fluorination with aminosulfuranes is a chemical reaction that transforms oxidized organic compounds into organofluorine compounds.Aminosulfuranes selectively exchange hydroxyl groups for fluorine, but are also capable of converting carbonyl groups, halides, silyl ethers, and other functionality into organofluorides.

  8. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Hydrogen bonding amongst HF molecules gives rise to high viscosity in the liquid phase and lower than expected pressure in the gas phase. Hydrogen fluoride does not boil until 20 °C in contrast to the heavier hydrogen halides which boil between −85 °C and −35 °C (−120 °F and –30 °F).

  9. Fluoroboric acid - Wikipedia

    en.wikipedia.org/wiki/Fluoroboric_acid

    The acidity of fluoroboric acid is complicated by the fact that its name refers to a range of different compounds, e.g. [H(CH 3 CH 2) 2 O] + [BF 4] − (dimethyloxonium tetrafluoroborate), [H 3 O] + [BF 4] − (oxonium tetrafluoroborate), and HF·BF 3 (hydrogen fluoride-boron trifluoride 1:1 adduct) – each with a different acidity.