in Wittig reaction intermediates formed are
a) Carbene b) Nitrene
d) Betain
Carbocation
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(2+2) Cycloaddition of the ylide to the carbonyl forms a four-membered cyclic intermediate, an oxaphosphetane. Preliminary posultated mechanisms lead first to a betaine as a zwitterionic intermediate, which would then close to the oxaphosphetane.
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