A Wagner-Meerwein rearrangement is a group of carbocation 1,2-rearrangement reactions in which a hydrogen, aryl or alkyl group shifts from one carbon to a neighboring carbon.
The rearrangement was first founded in bicyclic terpenes for instance the conversion of isoborneol to camphene:
![1513_Wagner–Meerwein-rearrangement.png](https://www.expertsmind.com/../CMSImages/1513_Wagner–Meerwein-rearrangement.png)
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