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  2. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    The addition of halogens to alkenes proceeds via intermediate halonium ions. In special cases, such intermediates have been isolated. [5] Bromination is more selective than chlorination because the reaction is less exothermic. Illustrative of the bromination of an alkene is the route to the anesthetic halothane from trichloroethylene: [6]

  3. Halogen - Wikipedia

    en.wikipedia.org/wiki/Halogen

    The other aliphatic-halogen bonds are weaker, their reactivity increasing down the periodic table. They are usually more chemically reactive than aliphatic C-H bonds. As a consequence, the most common halogen substitutions are the less reactive aromatic fluorine and chlorine groups.

  4. Aliphatic compound - Wikipedia

    en.wikipedia.org/wiki/Aliphatic_compound

    Aliphatic compounds can be saturated, joined by single bonds (), or unsaturated, with double bonds or triple bonds ().If other elements (heteroatoms) are bound to the carbon chain, the most common being oxygen, nitrogen, sulfur, and chlorine, it is no longer a hydrocarbon, and therefore no longer an aliphatic compound.

  5. Iodine compounds - Wikipedia

    en.wikipedia.org/wiki/Iodine_compounds

    By the same token, however, since iodine has the lowest ionisation energy among the halogens and is the most easily oxidised of them, it has a more significant cationic chemistry and its higher oxidation states are rather more stable than those of bromine and chlorine, for example in iodine heptafluoride. [1]

  6. Electrophilic halogenation - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_halogenation

    Halogenation of benzene where X is the halogen, catalyst represents the catalyst (if needed) and HX represents the protonated base. A few types of aromatic compounds, such as phenol, will react without a catalyst, but for typical benzene derivatives with less reactive substrates, a Lewis acid is required as a catalyst.

  7. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    Phenylic hydrogens have extremely strong bonds and are rarely displaced by halogens. Non-enolizable aldehydes oxidize to the acyl halide, but enolizable aldehydes typically halogenate at the α position instead. Indeed, allylic and benzylic hydrogens have bonds much weaker than alkanes, and are selectively replaced in the Wohl-Ziegler reaction.

  8. Saturated and unsaturated compounds - Wikipedia

    en.wikipedia.org/wiki/Saturated_and_unsaturated...

    For organic compounds containing heteroatoms (other than C and H), the list of unsaturated groups is long but some common types are: carbonyl, e.g. ketones, aldehydes, esters, carboxylic acids (unsaturated) vs alcohol or ether (saturated) nitrile (unsaturated) vs amine (saturated) nitro (unsaturated) vs amine (saturated)

  9. Water-reactive substances - Wikipedia

    en.wikipedia.org/wiki/Water-reactive_substances

    Halogens are so named due to their potential to form salts, and form many simple strong acids with hydrogen. Out of the four stable halogens, only fluorine and chlorine have reduction potentials higher than that of oxygen, allowing them to form hydrofluoric acid and hydrochloric acid directly through reaction with water. [17]