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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.
In a condensed phase, the carbocation can also gain an electron from surrounding molecules, thus becoming an electrically neutral radical. For example, in crystalline naphthalene, a molecule with tritium substituted for hydrogen in the 1 (or 2) position will be turned by decay into a cation with a positive charge at that position.
These free radicals may then react chemically with neighbouring materials even after the original radiation has stopped (e.g. ozone cracking of polymers by ozone formed by ionization of air). Ionizing radiation can also accelerate existing chemical reactions such as polymerization and corrosion, by contributing to the activation energy required ...
The hydroxyl radical, • HO, is the neutral form of the hydroxide ion (HO –). Hydroxyl radicals are highly reactive and consequently short-lived; however, they form an important part of radical chemistry .
In contemporary usage, the term radical refers to various free radicals, which are species that have an unpaired electron and need not be charged. [ citation needed ] [ 3 ] A simple example of a polyatomic ion is the hydroxide ion, which consists of one oxygen atom and one hydrogen atom, jointly carrying a net charge of −1 ; its chemical ...
Nitric oxide (nitrogen oxide or nitrogen monoxide [1]) is a colorless gas with the formula NO.It is one of the principal oxides of nitrogen.Nitric oxide is a free radical: it has an unpaired electron, which is sometimes denoted by a dot in its chemical formula (• N=O or • NO).
A free-radical reaction is any chemical reaction involving free radicals. This reaction type is abundant in organic reactions . Two pioneering studies into free radical reactions have been the discovery of the triphenylmethyl radical by Moses Gomberg (1900) and the lead-mirror experiment [ 1 ] described by Friedrich Paneth in 1927.
The molecular geometry of the methyl radical is trigonal planar (bond angles are 120°), although the energy cost of distortion to a pyramidal geometry is small. All other electron-neutral, non-conjugated alkyl radicals are pyramidalized to some extent, though with very small inversion barriers.