Chemistry
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ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Transcribed Image Text:3. Predict the products of the following Diels-Alder reactions.
a.
NC
a.
4. Identify the diene and dienophile used to make these Diel-Alder products.
CN
CH3
CN
CH 3
CO₂CH3
CO₂CH3
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- 2. a) Which of the following dienes could react in a Diels-Alder reaction: CH2 CH3 i) ii) CCH2 ii) H2c: `CH3 iv)arrow_forward21. Using MO diagrams, show that the [4+2] Diels-Alder is photochemically forbidden. CH2 hv CH2arrow_forward4. Using a Frost circle, approximate the relative energy level of the a molecular orbitals for following ions and justify the presence or absence of aromaticity in each. а. b.arrow_forward
- S1arrow_forwardPlease don't provide handwritten solution ....arrow_forward11. Which of the following Diels-Alder reactions will work? For example, if part a) is a viable Diels-Alder reaction: write A-yes. For all reactions that give a product; draw the structure of the resulting major product a) b) c) NHarrow_forward
- In the Diels Alder reaction what is Kinetically controlled product and what isthermodynamically controlled product? Give reasons.arrow_forwardWhat dene and dienophile is needed to prepare the following compound via a Diels-A der reaction? Choices A. a and b c and d e and f c and f C. D. b ane Ck Soe nd Submit to save andarrow_forward3. Show how Diels-Alder reactions might be used to synthesize the following compounds. a. Harrow_forward
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