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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.
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.
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 ...
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 ...
Most experimentally observed reactions are built up from many elementary reactions that occur in parallel or sequentially. The actual sequence of the individual elementary reactions is known as reaction mechanism. An elementary reaction involves a few molecules, usually one or two, because of the low probability for several molecules to meet at ...
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
Radical reactions must be carried out under inert atmosphere as dioxygen is a triplet radical which will intercept radical intermediates. Because the relative rates of a number of processes are important to the reaction, concentrations must be carefully adjusted to optimize reaction conditions.
One of the first pieces of experimental evidence for the existence of the solvent cage was the observation of the solvent cage effect on a crossover experiment. Since radical recombinations occur on very short timescales compared to non-radical reactions, the solvent cage effect is particularly relevant to radical chemistry. [5]