(a)
To determine: The product that is formed when given diene reacts with methyl acetylenecarboxylate, a strong dienophile.
Interpretation: The product that is formed when given diene reacts with methyl acetylenecarboxylate, a strong dienophile is to be stated.
Concept introduction: Diels-alder reaction is a cycloaddition reaction in which two molecules combine to form a new ring. In this type of reaction, syn addition takes place. It is a reaction between diene with a dienophile to yield a cyclohexene. The dienophile adds to one side of the diene, and the diene adds to the one side of the dienophile. Thus, they have syn stereochemistry. In Diels-Alder reaction, the diene behaves like an electron rich species, whereas the dienophile behaves like an electron poor species.
(b)
To determine: The path by which the strongly exothermic decarboxylation takes place.
Interpretation: The path by which the strongly exothermic decarboxylation takes place is to be stated.
Concept introduction: Diels-alder reaction is a cycloaddition reaction in which two molecules combine to form a new ring. In this type of reaction, syn addition takes place. It is a reaction between diene with a dienophile to yield a cyclohexene. The dienophile adds to one side of the diene, and the diene adds to the one side of the dienophile. Thus, they have syn stereochemistry.
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Chapter 15 Solutions
Organic Chemistry Plus Mastering Chemistry with Pearson eText -- Access Card Package (9th Edition) (New in Organic Chemistry)
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Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage Learning