9.46 Draw the substitution product formed (including stereochemistry) when (R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed by CH3l; (b) TsCI and pyridine, followed by NaOCH3; (c) PBг3, followed by NaOCH3. Which two routes produce identical products?
9.46 Draw the substitution product formed (including stereochemistry) when (R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed by CH3l; (b) TsCI and pyridine, followed by NaOCH3; (c) PBг3, followed by NaOCH3. Which two routes produce identical products?
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
Chapter11: Ethers, Epoxides, And Sulfides
Section: Chapter Questions
Problem 11.26P: Acid-catalyzed hydrolysis of the following epoxide gives a trans diol. Of the two possible trans...
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![9.46
Draw the substitution product formed (including stereochemistry) when
(R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed
by CH3l; (b) TsCI and pyridine, followed by NaOCH3; (c) PBг3, followed
by NaOCH3. Which two routes produce identical products?](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F39f6380b-55e3-47ff-8091-2f92e2b304db%2Fb2d32281-bb41-4836-9194-331c9177627a%2Fwg7gky5i_processed.jpeg&w=3840&q=75)
Transcribed Image Text:9.46
Draw the substitution product formed (including stereochemistry) when
(R)-hexan-2-ol is treated with each series of reagents: (a) NaH, followed
by CH3l; (b) TsCI and pyridine, followed by NaOCH3; (c) PBг3, followed
by NaOCH3. Which two routes produce identical products?
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