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1. Give the structures of the products obtained when the following are heated: Ph „Me -OMe b. a. Ph С. NC. CN + d. Which comp oundo would vou beot tegother in order to

1. Give the structures of the products obtained when the following are heated: Ph „Me -OMe b. a. Ph С. NC. CN + d. Which comp oundo would vou beot tegother in order to

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
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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1. Give the structures of the products obtained when the following are heated: Ph Me -OMe b. а. O2N Ph NC. CN C. d. 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:1. Give the structures of the products obtained when the following are heated: Ph Me -OMe b. а. O2N Ph NC. CN C. d. 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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