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  2. Fluoroalcohol - Wikipedia

    en.wikipedia.org/wiki/Fluoroalcohol

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  3. 2-Fluoroethanol - Wikipedia

    en.wikipedia.org/wiki/2-Fluoroethanol

    2-Fluoroethanol is the organic compound with the formula CH 2 FCH 2 OH. This colorless liquid is one of the simplest stable fluorinated alcohols. It was once used as a pesticide. The related difluoro- and trifluoroethanols are far less dangerous. [4]

  4. Pentafluorophenol - Wikipedia

    en.wikipedia.org/wiki/Pentafluorophenol

    Pentafluorophenol is the organofluorine compound (specifically a fluoroalcohol) with the formula C 6 F 5 OH. This is the perfluorinated analogue of phenol. It is a white solid that melts just above room temperature, and smells of phenol. With a pK a of 5.5, it is one of the most acidic phenols.

  5. Alcohol (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Alcohol_(chemistry)

    With strong bases such as sodium hydride or sodium they form salts [a] called alkoxides, with the general formula RO − M + (where R is an alkyl and M is a metal). R−OH + NaH → R−O − Na + + H 2 2 R−OH + 2 Na → 2 R−O − Na + + H 2. The acidity of alcohols is strongly affected by solvation. In the gas phase, alcohols are more ...

  6. Hexafluoro-2-propanol - Wikipedia

    en.wikipedia.org/wiki/Hexafluoro-2-propanol

    Hexafluoroisopropanol, commonly abbreviated HFIP, is the organic compound with the formula (CF 3) 2 CHOH. This fluoroalcohol finds use as solvent in organic chemistry. [1] Hexafluoro-2-propanol is transparent to UV light with high density, low viscosity and low refractive index. It is a colorless, volatile liquid with a pungent odor.

  7. Fluorotelomer alcohol - Wikipedia

    en.wikipedia.org/wiki/Fluorotelomer_alcohol

    The synthesis of fluorotelomer alcohols requires a varying number of tetrafluoroethylene monomers that form an oligomer with a pentafluoroethyl iodide telogen. The fluorinated iodide then undergoes an addition with ethylene to form an organoiodine compound with increased synthesis possibilities. [1]

  8. Nonafluoro-tert-butyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Nonafluoro-tert-butyl_alcohol

    Nonafluoro-tert-butyl alcohol (IUPAC name: 1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-ol) is a fluoroalcohol. It is the perfluorinated analog of tert-butyl alcohol. Notably, as a consequence of its electron withdrawing fluorine substituents, it is very acidic for an alcohol, with a pK a value of 5.4, similar to that of a carboxylic acid.

  9. Arrhenius equation - Wikipedia

    en.wikipedia.org/wiki/Arrhenius_equation

    In physical chemistry, the Arrhenius equation is a formula for the temperature dependence of reaction rates.The equation was proposed by Svante Arrhenius in 1889, based on the work of Dutch chemist Jacobus Henricus van 't Hoff who had noted in 1884 that the van 't Hoff equation for the temperature dependence of equilibrium constants suggests such a formula for the rates of both forward and ...