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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.
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.
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).
With the extra metal in the catalyst yield of the isomer can be 98% compared with the unsymmetrical isomer. [2] Mixed with perfluorooctane, it is a solvent for polydimethylsiloxane. [3] CFC-112 can be prepared as a mixture with other hydrochlorofluorocarbons from trichloroethylene and anhydrous hydrogen fluoride when electric current is passed ...
4 serves as a fluorine source to deliver an equivalent of fluoride. [2] The Balz–Schiemann reaction for the synthesis of aryl fluorides is the best known example of such a reaction. [3] Ether and halopyridine adducts of HBF 4 have been reported to be effective reagents for the hydrofluorination of alkynes. [4]
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.
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.
Though hydrogen fluoride is normally regarded as an exceptionally weak proton acceptor (though a somewhat better one than the SbF 6 – anion), dissociation of its protonated form, the fluoronium ion H 2 F + to HF and the truly naked H + is still a highly endothermic process (ΔG° = +113 kcal/mol), and imagining the proton in the condensed ...