Favorskii Rearrangement
It's the Favorskii rearrangement, a method of ring contraction! This reaction utilizes cyclopropane intermediates and is super neat. Need to make your ring one carbon smaller? Try the Favorskii rearrangement! Watch the whole Organic Chemistry playlist: http://bit.ly/ProfDaveOrgChem General Chemistry Tutorials: http://bit.ly/ProfDaveGenChem Biochemistry Tutorials: http://bit.ly/ProfDaveBiochem Biology Tutorials: http://bit.ly/ProfDaveBio Classical Physics Tutorials: http://bit.ly/ProfDavePhysics1 Modern Physics Tutorials: http://bit.ly/ProfDavePhysics2 Mathematics Tutorials: http://bit.ly/ProfDaveMath EMAIL► [email protected] PATREON► / professordaveexplains Check out "Is This Wi-Fi Organic?", my book on disarming pseudoscience! Amazon: https://amzn.to/2HtNpVH Bookshop: https://bit.ly/39cKADM Barnes and Noble: https://bit.ly/3pUjmrn Book Depository: http://bit.ly/3aOVDlT

Nef Reaction (Introduction to Umpolung Chemistry)

Curtius Rearragement

Carbenes Part 1: Properties and Formation

Favorskii Rearrangement # Organic Name Reaction Mechanism # with solved Examples

Beckmann Rearrangement

Adding Multiple Species to a Jurassic Park Lagoon

What If Humanity Never Masters Fusion?

The Hofmann Rearrangement--Rxn and Mechanism

Favorskii Rearrangement

Mitsunobu Reaction

IUPAC Nomenclature of Alkanes: Part 1

Pericyclic Reactions Part 3: Sigmatropic Shifts (Cope Rearrangement, Claisen Rearrangement)

Carbenes Part 2: Cyclopropanation, C-H Insertion, and the Bamford-Stevens Reaction

Pinacol Rearrangement Reaction of Diols into Ketones

Oxidation of alkenes by hot concentrated KMnO4

Biginelli Reaction

Claisen Condensation and Dieckmann Condensation

Favorskii Rearrangement Detailed Overview

Robinson Annulation

