Beckmann rearrangement

Beckmann rearrangement

Auto-curated
Playing 1/13
  • Beckmann rearrangement

    YouTube 03:54
  • Beckmann Rearrangement

    YouTube 01:21
  • Beckmann Rearrangement Mechanism | Organic Chemistry

    YouTube 02:10
  • Beckmann Rearrangement Example Mechanism | Organic Chemistry

    YouTube 02:11
  • Beckmann Rearrangement - Oxime Conversion to Nitrile Mechanism

    YouTube 02:20
  • What is Ethanol | Preparation & Properties of Ethanol | Uses & Chemical Properties of Ethanol

    YouTube 06:28
  • NYLON

    YouTube 01:49
  • GCSE Chemistry - Carboxylic Acids #69

    YouTube 03:05
  • Fluoride Ion Battery Research

    YouTube 00:30
  • Boiling Point of Organic compound(Aniline)

    YouTube 12:41
  • What Are Catalysts? | Reactions | Chemistry | FuseSchool

    YouTube 03:34
  • Ketone Identification Test Organic Compounds

    YouTube 03:50
  • How to Write the Formula for Carbon tetrachloride

    YouTube 01:07

The Beckmann rearrangement, named after the German chemist Ernst Otto Beckmann (1853–1923), is a rearrangement of an oxime functional group to substituted amides. The rearrangement has also been successful performed on haloimines and nitrones. Cyclic oximes and haloimines yield lactams.

Discover in context

This site is not available in the landscape mode.
Please rotate your phone or install our app.