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Answer:
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: 2R–X + 2Na → R–R + 2Na+X
An alkyl group can be added to a benzene molecule by an electrophile aromatic substitution reaction called the Friedel‐Crafts alkylation reaction. One example is the addition of a methyl group to a benzene ring. ... The electrophile attacks the π electron system of the benzene ring to form a nonaromatic carbocation.
The Kolbe electrolysis involves the formation of symmetrical hydrocarbons through the coupling of radicals generated from carboxylic acid at an anode via electrolysis. ... This reaction is useful for the preparation of hydrocarbons.
Explanation:
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