Why does the alkoxide anion dont act as a nucleophile in the fevorskii rearrangement? It can displace halide as halide is alpha to carbonyl and carbonyl decreses the energy of c-halide lumo

  • 2
    $\begingroup$ It can but because intremolecule reactions are much faster then intermolecular reactions you get mostly the rearrangement product. $\endgroup$ – Waylander Jan 11 at 15:46
  • 2
    $\begingroup$ SN2 reactions on secondary alkyl halides is not that fast. $\endgroup$ – Zhe Jan 11 at 21:30

Your Answer

By clicking "Post Your Answer", you acknowledge that you have read our updated terms of service, privacy policy and cookie policy, and that your continued use of the website is subject to these policies.

Browse other questions tagged or ask your own question.