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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. [1] [2] With some exceptions, these unpaired electrons make radicals highly chemically reactive. Many radicals spontaneously dimerize. Most ...
For example, the increase in temperature, drought are factors that limit the availability of CO 2 due to stomatal closure, increasing the production of ROS, such as O 2 ·- and 1 O 2 in chloroplasts. [ 33 ] [ 34 ] The production of 1 O 2 in chloroplasts can cause reprogramming of the expression of nucleus genes leading to chlorosis and ...
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 ...
List of inorganic compounds. ... (only simple oxides, oxyhalides, and related compounds, not hydroxides, carbonates, acids, or other compounds listed elsewhere) P
This list may not reflect recent changes. Free radical; Radical (chemistry) * Disposable soma theory of aging; Free-radical theory of aging; A. 4-Acetamido-TEMPO;
is an alkaline solution of potassium permanganate; used in organic chemistry as a qualitative test for the presence of unsaturation, such as double bonds; N-Bromosuccinimide: used in radical substitution and electrophilic addition reactions in organic chemistry. Also acts as a mild oxidizer to oxidize benzylic or allylic alcohols.
In chemistry, radical initiators are substances that can produce radical species under mild conditions and promote radical reactions. [1] These substances generally possess weak bonds—bonds that have small bond dissociation energies. Radical initiators are utilized in industrial processes such as polymer synthesis.
Another important class of radical substitutions involve aryl radicals. One example is the hydroxylation of benzene by Fenton's reagent. Many oxidation and reduction reactions in organic chemistry have free radical intermediates, for example the oxidation of aldehydes to carboxylic acids with chromic acid.