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

Cornerstones of Cost Management (Cornerstones Series)

4th Edition

ISBN:9781305970663

Author:Don R. Hansen, Maryanne M. Mowen

Publisher:Don R. Hansen, Maryanne M. Mowen

Chapter20: Inventory Management: Economic Order Quantity, Jit, And The Theory Of Constraints

Section: Chapter Questions

Problem 14E: Hales Company produces a product that requires two processes. In the first process, a subassembly is...

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