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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Which compound from the list below can undergo a Diels-Alder reaction?
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Which constitutional isomer represents the product of this Diels-Alder reaction?
9. For the following Diels-Alder products, propose the correct starting materials needed. D. a. b. C. fo{- ●●● Xox -
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?
Compounds P and Q can undergo a Diels-Alder reaction to form two regioisomeric products R and S as shown in Figure 5. OMe O C8H12O2 R C8H12O2 S Figure 5 Draw the chemical structures of regioisomeric compounds R and S. Using possible resonance contributors of P and Q predict which of the two regioisomers will be favoured in the reaction. Using curly arrows, draw the mechanism for the reaction of P and Q to form the dominant regioisomer you have predicted in your answer to part (ii) above.

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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