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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.
Radical disproportionation encompasses a group of reactions in organic chemistry in which two radicals react to form two different non-radical products. Radicals in chemistry are defined as reactive atoms or molecules that contain an unpaired electron or electrons in an open shell. The unpaired electrons can cause radicals to be unstable and ...
Organobismuth radical is a chemical species that has unpaired electrons on bismuth centers within organic frameworks. [1] These radicals are part of the broader family of pnictogen -centered radicals , which include nitrogen , phosphorus , arsenic , antimony , and bismuth . [ 2 ]
Radical theory is an obsolete scientific theory in chemistry describing the structure of organic compounds. The theory was pioneered by Justus von Liebig , Friedrich Wöhler and Auguste Laurent around 1830 and is not related to the modern understanding of free radicals .
Inorganic peroxides function analogously to organic peroxides. Many polymers are often produced from the alkenes upon initiation with peroxydisulfate salts. In solution, peroxydisulfate dissociates to give sulfate radicals: [3] [O 3 SO-OSO 3] 2− ⇌ 2 [SO 4] −. The sulfate radical adds to an alkene forming radical sulfate esters, e.g. .
In organic chemistry, a radical-substitution reaction is a substitution reaction involving free radicals as a reactive intermediate. [1] The reaction always involves at least two steps, and possibly a third. In the first step called initiation (2,3), a free radical is created by homolysis.
Hydroxyl radicals are also produced during UV-light dissociation of H 2 O 2 (suggested in 1879) and likely in Fenton chemistry, where trace amounts of reduced transition metals catalyze peroxide-mediated oxidations of organic compounds. In organic synthesis hydroxyl radicals are most commonly generated by photolysis of 1-Hydroxy-2(1H ...
In free radical polymerization, radicals formed from the decomposition of an initiator molecule are surrounded by a cage consisting of solvent and/or monomer molecules. [6] Within the cage, the free radicals undergo many collisions leading to their recombination or mutual deactivation. [5] [6] [9] This can be described by the following reaction: