In Wittig reaction, the methyl, primary and secondary alkyl halide use

Question

In Wittig reaction, the methyl, primary and secondary alkyl halide used to prepare Witting reagent(ylide) but not tertiary.

22 Jan 2021

Answer :

Word Count : 272

The Wittig reaction is a powerful method for the synthesis of alkenes from aldehydes or ketones. It involves the use of a Wittig reagent, also known as a phosphorane or ylide, which reacts with a carbonyl compound to form an alkene. The key step in the Wittig reaction is the formation of the ylide, _______ _____ ________ ________ _____ _________ _____ ________ ______ _______.
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