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The reactants can be found by the retrosynthesis of the given product which is as follows: 130 -1.0 but-3-en-2-one (Dienophile) 2,3-dimethylenetetrahydro-2H-pyran (Diene) The reaction is an example of Diels-alder reaction. The above two diene and dienophiles are the reactants for the reaction. The forward synthesis of the reaction is as follows: Heat In presence of heat, the diene and dienophile do cyclization reaction and make the product. Therefore, the reactants are as follows: but-3-en-2-one 2,3-dimethylenetetrahydro-2H-pyran

The reactants can be found by the retrosynthesis of the given product which is as follows: 130 -1.0 but-3-en-2-one (Dienophile) 2,3-dimethylenetetrahydro-2H-pyran (Diene) The reaction is an example of Diels-alder reaction. The above two diene and dienophiles are the reactants for the reaction. The forward synthesis of the reaction is as follows: Heat In presence of heat, the diene and dienophile do cyclization reaction and make the product. Therefore, the reactants are as follows: but-3-en-2-one 2,3-dimethylenetetrahydro-2H-pyran

Essentials Of Investments
Essentials Of Investments
11th Edition
ISBN:9781260013924
Author:Bodie, Zvi, Kane, Alex, MARCUS, Alan J.
Publisher:Bodie, Zvi, Kane, Alex, MARCUS, Alan J.
Chapter1: Investments: Background And Issues
Section: Chapter Questions
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The reactants can be found by the retrosynthesis of the given product which is as follows: 130 -1.0 but-3-en-2-one (Dienophile) 2,3-dimethylenetetrahydro-2H-pyran (Diene) The reaction is an example of Diels-alder reaction. The above two diene and dienophiles are the reactants for the reaction. The forward synthesis of the reaction is as follows: Heat In presence of heat, the diene and dienophile do cyclization reaction and make the product. Therefore, the reactants are as follows: but-3-en-2-one 2,3-dimethylenetetrahydro-2H-pyran
Transcribed Image Text:The reactants can be found by the retrosynthesis of the given product which is as follows: 130 -1.0 but-3-en-2-one (Dienophile) 2,3-dimethylenetetrahydro-2H-pyran (Diene) The reaction is an example of Diels-alder reaction. The above two diene and dienophiles are the reactants for the reaction. The forward synthesis of the reaction is as follows: Heat In presence of heat, the diene and dienophile do cyclization reaction and make the product. Therefore, the reactants are as follows: but-3-en-2-one 2,3-dimethylenetetrahydro-2H-pyran
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