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Dienes, Conjugated Pi Systems, and Pericyclic Reactions
Temperature and Diels–Alder Reaction Reversibility
Description
The Diels–Alder reaction is thermally reversible. At suitable temperatures, it can return to the starting diene and dienophile. The forward reaction forms a cyclohexene derivative and is favored at low to medium temperatures.
The reverse process is called the retro-Diels–Alder reaction. It is a r...
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Transcript
The Diels–Alder is a reversible reaction where the reaction temperature strongly influences the equilibrium position.
Moderate temperatures favor the addition product, whereas high temperatures favor the reactants via the reverse reaction known as retro Diels–Alder.
But why?
Recall that the change in Gibbs free energy, ∆...
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