Grignard reagent.
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The Grignard reaction is an organometallic chemical reaction in which alkyl, allyl, vinyl, or aryl-magnesium halides add to a carbonyl group in an aldehyde or ketone.
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A Grignard reagent has a formula RMgX where X is a halogen, and R is an alkyl or aryl (based on a benzene ring) group. For the purposes of this page, we shall take R to be an alkyl group (e.g., CH3CH2MgBr). Grignard reagents are made by adding the halogenoalkane to small bits of magnesium in a flask containing ethoxyethane (commonly called diethyl ether or just "ether"). The flask is fitted with a reflux condenser, and the mixture is warmed over a water bath for 20 - 30 minutes.
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