Please explain each step please explain each step Draw the product(s) of the following Diels-Alder reaction. Explain the formation of theproduct(s) by suggesting a mechanism.OH+OH80F3F4A%LOF5MacBook AirF6об гF7*DIIF8OF9

Mechanism is given in the image.

Answered: Draw the product(s) of the following…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter14: Conjugated Compounds And Ultraviolet Spectroscopy

Section14.SE: Something Extra

Problem 40AP

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Draw the structure of the product of the Diels-Alder reaction below. OCH3 H₂C 11 NO-C=C-CN
Draw the structure of the product of the Diels-Alder reaction below. H3C CH3 O || O || + CH3OC-CEC-COCH3
True or False: Acetylene is a naturally occurring conjugated diene True or False: The Diels-Alder reaction has the stereochemistry of the dienophile is retained in the product. True or False: When looking at kinetic vs. thermodynamic products the kinetic product predominates at low temperature. True or False: the mechanism of the Diels-Alder reaction is three π bonds break; one σ bond and two π bonds form.
Mechanism The Diels-Alder reaction is part of a class of reactions known as a cycloaddition reaction. This reaction is specifically a [4+2] cycloaddition which is a concerted (one-step) process in which two new carbon - carbon sigma bonds are formed from two pi bonds. For the first Diels - Alder step of the mechanism fill in the arrows needed for the transformation. The rest of the mechanism is drawn for you. OH Show mechanism arrows for this step! 4 + 2 cycloaddition OH H D- & H+ transfer OH Nuc acyl substitution H L.G.
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What is the diene and dienophile?
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Which of the following diene(s) cannot undergo the Diels-Alder reaction? II IV %3D
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The following is an example of a hetero Diels-Alder reaction, because a noncarbon atom (in this case, an N atom) is involved in bond formation and bond breaking. Draw the curved arrows necessary to account for this transformation. OCH3 OCH3 + N- Hydroquinone, benzene, 25 °C, 90 min 86%
4) Identify the reagents to prepare the following compound via Diels-Alder reaction Coalf DI Caotl a) X + .wolt •Looft b) x + you to c) of + Xco coot الاك d) None
Use arrows to predict the final favored product of the following Diels-Alder reaction. Use the step-wise mechanism to predict the final product of the following reaction. Show stereochemistry at stereogenic centers. NaBH4 CH;OH Use the step-wise mechanism to predict the product of the following reaction. (Excess) H.

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Draw the product(s) of the following Diels-Alder reaction. Explain the formation of the product(s) by suggesting a mechanism. OH + OH 80 F3 F4 A % L O F5 MacBook Air F6 об г F7 * DII F8 O F9