Named reactions: Wittig, Diels–Alder, Claisen, Dieckmann, Perkin
Advanced Organic (UG) · Chemistry
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Study notes
Let's trace the Diels–Alder reaction. Step 1: Take 1,3-butadiene (the diene) and ethene (the dienophile). Step 2: Imagine the electrons dancing. The double bonds shift to form two new single bonds and one new central double bond. Step 3: These two molecules fuse together. Result: You get cyclohexene, a 6-carbon ring. It is like building a box from two flat sheets of paper.