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The fluorine–fluorine bond of the difluorine molecule is relatively weak when compared to the bonds of heavier dihalogen molecules. The bond energy is significantly weaker than those of Cl 2 or Br 2 molecules and similar to the easily cleaved oxygen–oxygen bonds of peroxides or nitrogen–nitrogen bonds of hydrazines. [8]
Radical fluorination with the pure element is difficult to control and highly exothermic; care must be taken to prevent an explosion or a runaway reaction. With chlorine the reaction is moderate to fast; with bromine, slow and requires intense UV irradiation; and with iodine, it is practically nonexistent and thermodynamically unfavored.
Chlorine pentafluoride (ClF 5) is made on a large scale by direct fluorination of chlorine with excess fluorine gas at 350 °C and 250 atm, and on a small scale by reacting metal chlorides with fluorine gas at 100–300 °C. It melts at −103 °C and boils at −13.1 °C.
Such reagents include cobalt trifluoride, chlorine trifluoride, and iodine pentafluoride. [4] The method electrochemical fluorination is used commercially for the production of perfluorinated compounds. It generates small amounts of elemental fluorine in situ from hydrogen fluoride. The method avoids the hazards of handling fluorine gas.
A common preparative method involves fluorination of sodium hydroxide: 2 F 2 + 2 NaOH → OF 2 + 2 NaF + H 2 O. OF 2 is a colorless gas at room temperature and a yellow liquid below 128 K. Oxygen difluoride has an irritating odor and is poisonous. [3] It reacts quantitatively with aqueous haloacids to give free halogens: OF 2 + 4 HCl → 2 Cl 2 ...
Chlorine and oxygen can bond in a number of ways: chlorine monoxide radical, ClO•, chlorine (II) oxide radical; chloroperoxyl radical, ClOO•, chlorine (II) peroxide radical; chlorine dioxide, ClO 2, chlorine (IV) oxide; chlorine trioxide radical, ClO 3 •, chlorine (VI) oxide radical; chlorine tetroxide radical, ClO 4 •, chlorine (VII ...
Organofluorine compounds are prepared by numerous routes, depending on the degree and regiochemistry of fluorination sought and the nature of the precursors. The direct fluorination of hydrocarbons with F 2, often diluted with N 2, is useful for highly fluorinated compounds: R 3 CH + F 2 → R 3 CF + HF
The reaction at the anode results in chlorine gas from chlorine ions: 2 Cl − → Cl 2 + 2 e −. The reaction at the cathode results in hydrogen gas and hydroxide ions: 2 H 2 O + 2 e − → H 2 + 2 OH −. Without a partition between the electrodes, the OH − ions produced at the cathode are free to diffuse throughout the electrolyte to the ...