a. b. C. d. H3O+ 9. The acid-catalyzed hydrolysis of the epoxide drawn above will give a. A diol as a 50/50 mixture of enantiomers b. A diol as an enantiopure compound c. A diol as a meso compound d. No reaction 10. The reaction below is in equilibrium. Which of the following methods will help drive the reaction forward to form a near quantitative yield of products? Circle the entire answer and all answers that apply. OCH3 -OCH3 + H₂O + 2 CH3OH d Use a large excess of methanol Use a chiral reagent Distill off the water that is formed in the reaction Add a drying agent, such as sodium sulfate 5

a. b. C. d. H3O+ 9. The acid-catalyzed hydrolysis of the epoxide drawn above will give a. A diol as a 50/50 mixture of enantiomers b. A diol as an enantiopure compound c. A diol as a meso compound d. No reaction 10. The reaction below is in equilibrium. Which of the following methods will help drive the reaction forward to form a near quantitative yield of products? Circle the entire answer and all answers that apply. OCH3 -OCH3 + H₂O + 2 CH3OH d Use a large excess of methanol Use a chiral reagent Distill off the water that is formed in the reaction Add a drying agent, such as sodium sulfate 5

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter15: An Introduction To Organometallic Compounds

Section: Chapter Questions

Problem 15.17P

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