Answer:
The stereochemistry of the dienophile is retained in the product.
Explanation:
The main properties of the Diels-Alder reaction are:
- The diene can react only when it adopts the s-cis conformation.
- Electron-donating substituents in the diene increase reaction rate.
- Electron-withdrawing substituents in the dienophile increase reaction rate.
- The stereochemistry of the dienophile and of the diene is retained in the product.