Cope rearrangement
| Cope rearrangement | |
|---|---|
| Named after | Arthur C. Cope | 
| Reaction type | Rearrangement reaction | 
| Identifiers | |
| Organic Chemistry Portal | cope-rearrangement | 
| RSC ontology ID | RXNO:0000028 | 
The Cope rearrangement is an extensively studied organic reaction involving the [3,3]-sigmatropic rearrangement of 1,5-dienes. It was developed by Arthur C. Cope and Elizabeth Hardy. For example, 3-methyl-hexa-1,5-diene heated to 300 °C yields hepta-1,5-diene.
The Cope rearrangement causes the fluxional states of the molecules in the bullvalene family.