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  2. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Fluorine's chemistry is dominated by its strong tendency to gain an electron. It is the most electronegative element and elemental fluorine is a strong oxidant. The removal of an electron from a fluorine atom requires so much energy that no known reagents are known to oxidize fluorine to any positive oxidation state. [20]

  3. Electrophilic aromatic directing groups - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    Due to a stronger resonance effect and inductive effect than the heavier halogens, fluorine is anomalous. The partial rate factor of electrophilic aromatic substitution on fluorobenzene is often larger than one at the para position, making it an activating group. [11]

  4. Fluoride - Wikipedia

    en.wikipedia.org/wiki/Fluoride

    The tea plant (Camellia sinensis L.) is a known accumulator of fluorine compounds, released upon forming infusions such as the common beverage. The fluorine compounds decompose into products including fluoride ions. Fluoride is the most bioavailable form of fluorine, and as such, tea is potentially a vehicle for fluoride dosing. [29]

  5. Molar ionization energies of the elements - Wikipedia

    en.wikipedia.org/wiki/Molar_ionization_energies...

    This is the energy per mole necessary to remove electrons from gaseous atoms or atomic ions. The first molar ionization energy applies to the neutral atoms. The second, third, etc., molar ionization energy applies to the further removal of an electron from a singly, doubly, etc., charged ion.

  6. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    Fluorine is a chemical element; it has symbol F and atomic number 9. It is the lightest halogen [ note 1 ] and exists at standard conditions as pale yellow diatomic gas. Fluorine is extremely reactive as it reacts with all other elements except for the light noble gases .

  7. Radical fluorination - Wikipedia

    en.wikipedia.org/wiki/Radical_fluorination

    The O–F bond of hypofluorites is relatively weak. For trifluoromethyl hypofluorite (CF 3 OF), it has been estimated to be 43.5 kcal/mol (182 kJ/mol). [9] The ability of trifluoromethyl hypofluorite to transfer fluorine to alkyl radicals is notably demonstrated by reacting independently generated ethyl radicals from ethene and tritium in the presence of CF 3 OF. [10]

  8. Electrophilic fluorination - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_fluorination

    The mechanism of electrophilic fluorination remains controversial. At issue is whether the reaction proceeds via an S N 2 or single-electron transfer (SET) process. In support of the S N 2 mechanism, aryl Grignard reagents and aryllithiums give similar yields of fluorobenzene in combination with N-fluoro-o-benzenedisulfonimide (NFOBS), even though the tendencies of these reagents to ...

  9. Fluoroanion - Wikipedia

    en.wikipedia.org/wiki/Fluoroanion

    In chemistry, a fluoroanion or fluorometallate anion is a polyatomic anion that contains one or more fluorine atoms. The ions and salts form from them are also known as complex fluorides. They can occur in salts, or in solution, but seldom as pure acids. Fluoroanions often contain elements in higher oxidation states. They mostly can be ...