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  2. Interhalogen - Wikipedia

    en.wikipedia.org/wiki/Interhalogen

    Bromine pentafluoride (BrF 5) is a colourless fuming liquid, made by reacting bromine trifluoride with fluorine at 200 °C. It is physically stable, but decomposes violently on contact with water, organic substances, and most metals and nonmetals .

  3. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Fluorine's chemistry includes inorganic compounds formed with hydrogen, metals, nonmetals, and even noble gases; as well as a diverse set of organic compounds. [note 1] For many elements (but not all) the highest known oxidation state can be achieved in a fluoride. For some elements this is achieved exclusively in a fluoride, for others ...

  4. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Bromine is a weaker halogenating agent than both fluorine and chlorine, while iodine is the least reactive of them all. The facility of dehydrohalogenation follows the reverse trend: iodine is most easily removed from organic compounds, and organofluorine compounds are highly stable.

  5. Halogen - Wikipedia

    en.wikipedia.org/wiki/Halogen

    The halogens (/ ˈ h æ l ə dʒ ə n, ˈ h eɪ-,-l oʊ-,-ˌ dʒ ɛ n / [1] [2] [3]) are a group in the periodic table consisting of six chemically related elements: fluorine (F), chlorine (Cl), bromine (Br), iodine (I), and the radioactive elements astatine (At) and tennessine (Ts), though some authors [4] would exclude tennessine as its chemistry is unknown and is theoretically expected to ...

  6. Organobromine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organobromine_chemistry

    Bromine is more electronegative than carbon (2.9 vs 2.5). Consequently, the carbon in a carbon–bromine bond is electrophilic, i.e. alkyl bromides are alkylating agents. [2] Carbon–halogen bond strengths, or bond dissociation energies are of 115, 83.7, 72.1, and 57.6 kcal/mol for bonded to fluorine, chlorine, bromine, or iodine, respectively ...

  7. Dehalogenation - Wikipedia

    en.wikipedia.org/wiki/Dehalogenation

    Dehalogenations come in many varieties, including defluorination (removal of fluorine), dechlorination (removal of chlorine), debromination (removal of bromine), and deiodination (removal of iodine). Incentives to investigate dehalogenations include both constructive and destructive goals.

  8. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    Fluorine has several distinctive differences from all other substituents encountered in organic molecules. As a result, the physical and chemical properties of organofluorines can be distinctive in comparison to other organohalogens. The carbon–fluorine bond is one of the strongest in organic chemistry (an average bond energy around 480 kJ ...

  9. Bromine fluoride - Wikipedia

    en.wikipedia.org/wiki/Bromine_fluoride

    Bromine fluoride may refer to several compounds with the elements bromine and fluorine: Bromine monofluoride, BrF;