i. What starting materials would you use to prepare each of the following compounds by the Diels–Alder reaction?
ii. Diels–Alder reactions with benzene are rare, and require a very reactive (electron-deficient) dienophile, because benzene is a rather unreactive diene. Two are shown below. Give the structures of the product produced in each reaction.
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iii. Shown below are two heteroatom compounds that undergo the Diels–Alder reaction. Formulate the product obtained in each reaction.
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