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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.
Hydrogen fluoride is typically produced by the reaction between sulfuric acid and pure grades of the mineral fluorite: [14] CaF 2 + H 2 SO 4 → 2 HF + CaSO 4 About 20% of manufactured HF is a byproduct of fertilizer production, which generates hexafluorosilicic acid .
As fluorine is itself manufactured by the electrolysis of hydrogen fluoride, ECF is a rather more direct route to fluorocarbons. The process proceeds at low voltage (5 – 6 V) so that free fluorine is not liberated. The choice of substrate is restricted as ideally it should be soluble in hydrogen fluoride.
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.
HF is miscible with water (will dissolve in any proportion), while the other hydrogen halides have large solubility gaps with water. Hydrogen fluoride and water also form several compounds in the solid state, most notably a 1:1 compound that does not melt until −40 °C (−40 °F), which is 44 degrees Celsius (79 degrees Fahrenheit) above the ...
Hydrogen fluoride, a weak acid in aqueous solution that is normally not thought to have any appreciable Brønsted basicity at all, is in fact the strongest Brønsted base in the mixture, protonating to H 2 F + in the same way water protonates to H 3 O + in aqueous acid. It is the fluoronium ion that accounts for fluoroantimonic acid's extreme ...
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.
ClF 3 also reacts explosively with water to give hydrogen fluoride and hydrogen chloride, along with oxygen and oxygen difluoride (OF 2): [15] ClF 3 + H 2 O → HF + HCl + OF 2 ClF 3 + 2H 2 O → 3HF + HCl + O 2. Upon heating, it decomposes: [13] ClF 3 ⇌ ClF + F 2. Reactions with many metals and even metal oxides give fluorides: [15] 6NiO + 4 ...