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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.
The lighter noble gases xenon and krypton can be made to react with fluorine under special conditions, while argon will undergo chemical transformations only with hydrogen fluoride. [18] Nitrogen, with its very stable triple bonds, requires electric discharge and high temperatures to combine with fluorine directly. [19]
At high temperatures, heptafluoropropane will decompose and produce hydrogen fluoride. The decomposition produces a sharp, pungent odour, which can be perceived in concentrations far below a dangerous level. Other decomposition products include carbonyl fluoride, carbon monoxide and carbon dioxide. Prior to re-entry of a room where HFC-227ea ...
Perfluoroalkanes are very stable because of the strength of the carbon–fluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...
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.
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]
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 ...