Alkyl which alkyl halide is used in identification of ethylene / brainly
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Explanation:
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The Wurtz reaction, named after Charles Adolphe Wurtz, is a coupling reaction in organic chemistry, organometallic chemistry and recently inorganic main group polymers, whereby two alkyl halides are reacted with sodium metal in dry ether solution to form a higher alkane. In this reaction alkyl halides are treated with sodium metal in dry ethereal (free from moisture) solution to produce higher alkanes and it is also used for the preparation of higher alkanes containing even number of carbon atoms.
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Answer:
Organohalogen compound, any of a class of organic compounds that contain at least one halogen (fluorine [F], chlorine [Cl], bromine [Br], or iodine [I]) bonded to carbon. They are subdivided into alkyl, vinylic, aryl, and acyl halides. In alkyl halides all four bonds to the carbon that bears the halogen are single bonds; in vinylic halides the carbon that bears the halogen is doubly bonded to another carbon; in aryl halides the halogen-bearing carbon is part of an aromatic ring; and in acyl halides (also called acid halides) the halogen-bearing carbon is doubly bonded to oxygen.
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