Quinone
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Quinone
Benzoquinone, or quinone is one of the two isomers of cyclohexadienedione. These compounds have the molecular formula C6H4O2. Orthobenzoquinone is the 1,2-dione, whereas parabenzoquinone is the 1,4-dione. Orthobenzoquinone is the oxidized form of catechol (1,2-dihydroxybenzene), while parabenzoquinone is the oxidized form of hydroquinone. An acidic potassium iodide solution reduces a solution of benzoquinone to hydroquinone, which is oxidized back with a solution of silver nitrate. Quinone is also the name for the class of compounds containing either benzoquinone isomers as part of their structure. Quinones are not aromatic, but are diketones. <gallery> Image:orthobenzoquinone.svg|1,2-Benzoquinone Image:P-Benzochinon.svg|1,4-Benzoquinone Image:2,3,5,6-tetrachloro-parabenzoquinone.svg|p-chloranil Image:2,3-dicyano-5,6-dichloroparabenzoquinone.svg|DDQ </gallery> BiochemistryQuinone is a common constituent of biologically relevant molecules (e.g. Vitamin K1 is phylloquinone). Others serve as electron acceptors in electron transport chains such as those in Photosystems I & II of photosynthesis, and aerobic respiration. A natural example of the oxidization of hydroquinone to quinone is the spray of bombardier beetles. Hydroquinone is reacted with hydrogen peroxide to produce a fiery blast of steam, a strong deterrent in the animal world. Quinones can be partially reduced to quinols. Oxidizing agentsBenzoquinone is used in organic chemistry as an oxidizing agent. Stronger quinone oxidising agents exist; for instance: 2,3,5,6-tetrachloro-parabenzoquinone (also known as p-chloranil) and 2,3-dicyano-5,6-dichloro-parabenzoquinone (also known as DDQ). [1] Referencesda:Quinon de:Chinone es:Quinona fr:Quinone it:Chinoni nl:Chinon (chemie) ja:??? pl:Benzochinon pt:Quinona vi:Quinon zh:?
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