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Reactions of elemental fluorine with metals require varying conditions. Alkali metals cause explosions and alkaline earth metals display vigorous activity in bulk; to prevent passivation from the formation of metal fluoride layers, most other metals such as aluminium and iron must be powdered, [ 21 ] and noble metals require pure fluorine gas ...
Water-reactive substances [1] are those that spontaneously undergo a chemical reaction with water, often noted as generating flammable gas. [2] Some are highly reducing in nature. [ 3 ] Notable examples include alkali metals , lithium through caesium , and alkaline earth metals , magnesium through barium .
Reactions with elemental fluorine are often sudden or explosive. Many substances that are generally regarded as unreactive, such as powdered steel, glass fragments, and asbestos fibers, are readily consumed by cold fluorine gas. Wood and even water burn with flames when subjected to a jet of fluorine, without the need for a spark. [12] [13]
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. This acid can be degraded to release HF thermally and by hydrolysis: H 2 SiF ...
Oxygen difluoride reacts with water to form hydrofluoric acid: OF 2 + H 2 O → 2 HF + O 2. It can oxidize sulphur dioxide to sulfur trioxide and elemental fluorine: OF 2 + SO 2 → SO 3 + F 2. However, in the presence of UV radiation, the products are sulfuryl fluoride (SO 2 F 2) and pyrosulfuryl fluoride (S 2 O 5 F 2): OF 2 + 2 SO 2 → S 2 O ...
The reaction of F 2 with organic compounds is, however, highly exothermic and can lead to non-selective fluorinations and C–C cleavage, as well as explosions. [6] Only a few selective radical fluorination methods have been reported. [7] [8] The use of fluorine for radical fluorination is mainly limited to perfluorination reactions. [5]
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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 ...