The Cope rearrangement is an extensively studied organic reaction involving the -sigmatropic rearrangement of 1,5-dienes. It was developed by Arthur C. Cope. For example 3-methyl-1,5-hexadiene heated to 300°C yields 1,5-heptadiene.
The Cope rearrangement causes the fluxional states of the molecules in the bullvalene family.
Read more about Cope Rearrangement: Mechanism, Examples, Oxy-Cope Rearrangement, Variations
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