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8. Explain why the cis-diastereomer of the compound shown below reacts faster than the trans-diastereomer in an E2 reaction. Br 9. Ethers can often be prepared by SN2 reaction of alkoxide ions, RO, with alkyl halides. Suppose you wanted to prepare cyclohexyl methyl ether. Which of the following two possible routes would you choose? Explain. + CH3I OCH3 OR + CH3O

8. Explain why the cis-diastereomer of the compound shown below reacts faster than the trans-diastereomer in an E2 reaction. Br 9. Ethers can often be prepared by SN2 reaction of alkoxide ions, RO, with alkyl halides. Suppose you wanted to prepare cyclohexyl methyl ether. Which of the following two possible routes would you choose? Explain. + CH3I OCH3 OR + CH3O

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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8. Explain why the cis-diastereomer of the compound shown below reacts faster than the trans-diastereomer in an E2 reaction. Br 9. Ethers can often be prepared by SN2 reaction of alkoxide ions, RO, with alkyl halides. Suppose you wanted to prepare cyclohexyl methyl ether. Which of the following two possible routes would you choose? Explain. + CH3I OCH3 OR + CH3O
Transcribed Image Text:8. Explain why the cis-diastereomer of the compound shown below reacts faster than the trans-diastereomer in an E2 reaction. Br 9. Ethers can often be prepared by SN2 reaction of alkoxide ions, RO, with alkyl halides. Suppose you wanted to prepare cyclohexyl methyl ether. Which of the following two possible routes would you choose? Explain. + CH3I OCH3 OR + CH3O
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