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Describe the mechanism for the first chemical reaction indicated in this reaction scheme. You need not describe the second reaction. DIELS ALDER CHEMISTRY. Indicate the Diels Alder product formed in the reaction of compounds: Diels Alder product of the diene lactone and methyl acetylene carboxylate (indicated in above) is unstable. If heated, it decomposes to produce CO_2 and methyl benzoate which is very stable. Propose a mechanism for this decarboxylation. DIELS ALDER CHEMISTRY. Indicate the product of the intramolecular Diels-Alder of this compound. (You do not need to indicate stereochemistry.)
Describe the mechanism for the first chemical reaction indicated in this reaction scheme. You need not describe the second reaction. DIELS ALDER CHEMISTRY. Indicate the Diels Alder product formed in the reaction of compounds: Diels Alder product of the diene lactone and methyl acetylene carboxylate (indicated in above) is unstable. If heated, it decomposes to produce CO_2 and methyl benzoate which is very stable. Propose a mechanism for this decarboxylation. DIELS ALDER CHEMISTRY. Indicate the product of the intramolecular Diels-Alder of this compound. (You do not need to indicate stereochemistry.)
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Jarrod RobelLv2
10 Nov 2019
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