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  2. Hydrogen fluoride - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_fluoride

    Hydrogen fluoride does not boil until 20 °C in contrast to the heavier hydrogen halides, which boil between −85 °C (−120 °F) and −35 °C (−30 °F). [6] [7] [8] This hydrogen bonding between HF molecules gives rise to high viscosity in the liquid phase and lower than expected pressure in the gas phase.

  3. 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]

  4. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Fluorine's chemistry includes inorganic compounds formed with hydrogen, metals, nonmetals, and even noble gases; as well as a diverse set of organic compounds. [ note 1 ] For many elements (but not all) the highest known oxidation state can be achieved in a fluoride.

  5. Fluorination with aminosulfuranes - Wikipedia

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

    Attack of the hydroxyl group of the substrate on sulfur and elimination of hydrogen fluoride lead to an alkoxyaminosulfur difluoride intermediate. Nucleophilic attack by fluoride, either by an S N 1 [5] or S N 2 [6] pathway, leads to the product. Although clean configurational inversion has been observed in a number of chiral alcohols ...

  6. Electrochemical fluorination - Wikipedia

    en.wikipedia.org/wiki/Electrochemical_fluorination

    The Simons process, named after Joseph H. Simons entails electrolysis of a solution of an organic compound in a solution of hydrogen fluoride. An individual reaction can be described as: R 3 C–H + HF → R 3 C–F + H 2. In the course of a typical synthesis, this reaction occurs once for each C–H bond in the precursor.

  7. Fries rearrangement - Wikipedia

    en.wikipedia.org/wiki/Fries_rearrangement

    As an alternative to aluminium chloride, other Lewis acids such as boron trifluoride and bismuth triflate or strong protic acids such as hydrogen fluoride and methanesulfonic acid can also be used. [ citation needed ] In order to avoid the use of these corrosive and environmentally unfriendly catalysts altogether research into alternative ...

  8. 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.

  9. Monofluoride - Wikipedia

    en.wikipedia.org/wiki/Monofluoride

    Because the fluoride anion is highly basic, many alkali metal fluorides form bifluorides with the formula MHF 2. Sodium and potassium bifluorides are significant to the chemical industry. [ 2 ] Among other monofluorides, only silver(I) [ 3 ] and thallium(I) [ 4 ] fluorides are well-characterized.