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  2. Halide - Wikipedia

    en.wikipedia.org/wiki/Halide

    In chemistry, a halide (rarely halogenide [1]) is a binary chemical compound, of which one part is a halogen atom and the other part is an element or radical that is less electronegative (or more electropositive) than the halogen, to make a fluoride, chloride, bromide, iodide, astatide, or theoretically tennesside compound.

  3. Hydrogen halide - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_halide

    In chemistry, hydrogen halides (hydrohalic acids when in the aqueous phase) are diatomic, inorganic compounds that function as Arrhenius acids. The formula is HX where X is one of the halogens: fluorine, chlorine, bromine, iodine, astatine, or tennessine. [1] All known hydrogen halides are gases at standard temperature and pressure. [2]

  4. Category:Halides - Wikipedia

    en.wikipedia.org/wiki/Category:Halides

    The halogens may either be bonded to another element through covalent bonding or (as in many metal halides) present in the form of the halide ion. Subcategories This category has the following 13 subcategories, out of 13 total.

  5. Hunsdiecker reaction - Wikipedia

    en.wikipedia.org/wiki/Hunsdiecker_reaction

    The Hunsdiecker reaction (also called the Borodin reaction or the Hunsdiecker–Borodin reaction) is a name reaction in organic chemistry whereby silver salts of carboxylic acids react with a halogen to produce an organic halide. [1]

  6. Metal halides - Wikipedia

    en.wikipedia.org/wiki/Metal_halides

    Halide ligands may also be displaced by the alkali salt of an X-type ligand, such as a salen-type ligand. [10] This reaction is formally a transmetallation, and the abstraction of the halide is driven by the precipitation of the resultant alkali halide in an organic solvent. The alkali halides generally have very high lattice energies.

  7. Hydrohalogenation - Wikipedia

    en.wikipedia.org/wiki/Hydrohalogenation

    This is due to the abstraction of a hydrogen atom by the alkene from the hydrogen halide (HX) to form the most stable carbocation (relative stability: 3°>2°>1°>methyl), as well as generating a halogen anion. A simple example of a hydrochlorination is that of indene with hydrogen chloride gas (no solvent): [4]

  8. Halocarbon - Wikipedia

    en.wikipedia.org/wiki/Halocarbon

    Halocarbon compounds are chemical compounds in which one or more carbon atoms are linked by covalent bonds with one or more halogen atoms (fluorine, chlorine, bromine or iodine – group 17) resulting in the formation of organofluorine compounds, organochlorine compounds, organobromine compounds, and organoiodine compounds.

  9. Silver bromide - Wikipedia

    en.wikipedia.org/wiki/Silver_bromide

    The larger halide ions are arranged in a cubic close-packing, while the smaller silver ions fill the octahedral gaps between them, giving a 6-coordinate structure where a silver ion Ag + is surrounded by 6 Br − ions, and vice versa. The coordination geometry for AgBr in the NaCl structure is unexpected for Ag(I) which typically forms linear ...