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(Solved): 5. what is the structure of the intramolecular Diels-Alder product of the compound shown?6. two cons ...
5. what is the structure of the intramolecular Diels-Alder product of the compound shown?
6. two constitutional isomers of molecular formula C8H12O are formed in the following reaction. Ignoring stereochemistry, suggest reasonable structures for these Diels-Alder adducts.
7. Allene can be converted to a trimer (compound A) of the molecular formula if C9H12. Compound A reacts with dimethyl acetylenedicarboxylate to give compound B. Deduce the structure of compound A.
5) What is the structure of the intramolecular Diels-Alder product of the compound shown? (No need to show stereochemistry.) A 8 C. D. 6. Two constitutional isomers of molecular formula are formed in the following reaction. Ignoring stereochemistry, suggest reasonable structures for these Diels-Alder adducts. heat 7. Allene can be converted to a trimer (compound A) of molecular formula . Compound reacts with dimethyl acetylenedicarboxylate to give compound . Deduce the structure of compound A. Compound B
Expert Answer
5) The solution of this question is given below;