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no reaction. A diene trand in nakere, it will not undorgo diela aldri reaction.

no reaction. A diene trand in nakere, it will not undorgo diela aldri reaction.

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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1. ph a. Me. [4+2J Me Ph Ph O b. Me Me. cyloaddition NC CN CN. yeocaddition d. no reaction. A dieme i trane in naterre, it will n undergo diel's aldr reachton.
Transcribed Image Text:1. ph a. Me. [4+2J Me Ph Ph O b. Me Me. cyloaddition NC CN CN. yeocaddition d. no reaction. A dieme i trane in naterre, it will n undergo diel's aldr reachton.
2. Which compounds would you heat together in order to synthesize each of the following? CHO 3. The 1,4-diphenyl-1,3-butadiene that you used is the (E,E)-isomer. The phenyl cis groups in your product are other. with respect STEREOCHEMICAL FORMULAS, explain to each USING why the (E,E)- diene gives an adduct in which the phenyl groups are cis. (HINT: Remember that there is free rotation around single bonds, and study the Diels- discussion of the stereochemistry of the Alder reaction in your text.)
Transcribed Image Text:2. Which compounds would you heat together in order to synthesize each of the following? CHO 3. The 1,4-diphenyl-1,3-butadiene that you used is the (E,E)-isomer. The phenyl cis groups in your product are other. with respect STEREOCHEMICAL FORMULAS, explain to each USING why the (E,E)- diene gives an adduct in which the phenyl groups are cis. (HINT: Remember that there is free rotation around single bonds, and study the Diels- discussion of the stereochemistry of the Alder reaction in your text.)
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Step 1

Here we have to determine the starting material required to prepare the given adduct. We can solve this by retro -diel's alder reaction. 

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