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  2. Radical (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Radical_(chemistry)

    The hydroxyl radical, Lewis structure shown, contains one unpaired electron. Lewis dot structure of a Hydroxide ion compared to a hydroxyl radical. In chemistry, a radical, also known as a free radical, is an atom, molecule, or ion that has at least one unpaired valence electron.

  3. Hydroxyl radical - Wikipedia

    en.wikipedia.org/wiki/Hydroxyl_radical

    The hydroxyl radical has a very short in vivo half-life of approximately 10 −9 seconds and a high reactivity. [5] This makes it a very dangerous compound to the organism. [6] [7] Unlike superoxide, which can be detoxified by superoxide dismutase, the hydroxyl radical cannot be eliminated by an enzymatic reaction.

  4. Reactive oxygen species - Wikipedia

    en.wikipedia.org/wiki/Reactive_oxygen_species

    Hydroxyl radical (HO·) is generated by Fenton reaction of hydrogen peroxide with ferrous compounds and related reducing agents: Fe(II) + H 2 O 2 → Fe(III)OH + HO· In its fleeting existence, the hydroxyl radical reacts rapidly irreversibly with all organic compounds. superoxide (O − 2) is produced by reduction of O 2. [4]

  5. Free-radical reaction - Wikipedia

    en.wikipedia.org/wiki/Free-radical_reaction

    Reaction inhibitors slow down a radical reaction and radical disproportionation is a competing reaction. Radical reactions occur frequently in the gas phase, are often initiated by light, are rarely acid or base catalyzed and are not dependent on polarity of the reaction medium. [2] Reactions are also similar whether in the gas phase or ...

  6. Free-radical addition - Wikipedia

    en.wikipedia.org/wiki/Free-radical_addition

    These reactions can happen due to the free radicals having an unpaired electron in their valence shell, making them highly reactive. [1] Radical additions are known for a variety of unsaturated substrates, both olefinic or aromatic and with or without heteroatoms. Free-radical reactions depend on one or more relatively weak bonds in a

  7. Peters four-step chemistry - Wikipedia

    en.wikipedia.org/wiki/Peters_four-step_chemistry

    The third reaction, known as radical consumption layer, where most of the heat is released, and the first reaction, also known as fuel consumption layer, occur in a narrow region at the flame. The fourth reaction is the hydrogen oxidation layer, whose thickness is much larger than the former two layers.

  8. Trivalent group 14 radicals - Wikipedia

    en.wikipedia.org/wiki/Trivalent_group_14_radicals

    A trivalent group 14 radical (also known as a trivalent tetrel radical) is a molecule that contains a group 14 element (E = C, Si, Ge, Sn, Pb) with three bonds and a free radical, having the general formula of R 3 E•. Such compounds can be categorized into three different types, depending on the structure (or equivalently the orbital in which ...

  9. Sulfanyl - Wikipedia

    en.wikipedia.org/wiki/Sulfanyl

    Sulfanyl (HS •), also known as the mercapto radical, hydrosulfide radical, or hydridosulfur, is a simple radical molecule consisting of one hydrogen and one sulfur atom. The radical appears in metabolism in organisms as H 2 S is detoxified. Sulfanyl is one of the top three sulfur-containing gasses in gas giants such as Jupiter and is very ...