Under acid-catalyzed conditions, epoxides can be opened by a variety of nucleophiles other than water, such as alcohols. In such a case, the nucleophile will generally attack at the more substituted position. Using this information, predict the products for each of the following reactions (a-b): 1) ROO ? Modify the given structure to draw the major product(s). Use the single bond tool to interconvert between double and single bonds. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. Edit Drawing
Under acid-catalyzed conditions, epoxides can be opened by a variety of nucleophiles other than water, such as alcohols. In such a case, the nucleophile will generally attack at the more substituted position. Using this information, predict the products for each of the following reactions (a-b): 1) ROO ? Modify the given structure to draw the major product(s). Use the single bond tool to interconvert between double and single bonds. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and Paste to save drawing time. Edit Drawing
Chapter17: Alcohols And Phenols
Section17.SE: Something Extra
Problem 30MP
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![Under acid-catalyzed conditions, epoxides can be opened by a variety of nucleophiles other than water, such as alcohols. In such a
case, the nucleophile will generally attack at the more substituted position. Using this information, predict the products for each
of the following reactions (a-b):
?
1) RCO-H
2) [H₂SOJ
Modify the given structure to draw the major product(s). Use the single bond tool to interconvert between double and single
bonds. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and
Paste to save drawing time.
CH₂
Edit Drawing
A](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb0070665-0daf-491d-9fa6-04053ba89e9f%2Ff664928d-eda9-4638-9866-be52ac0b6481%2Fzfo4c9l_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Under acid-catalyzed conditions, epoxides can be opened by a variety of nucleophiles other than water, such as alcohols. In such a
case, the nucleophile will generally attack at the more substituted position. Using this information, predict the products for each
of the following reactions (a-b):
?
1) RCO-H
2) [H₂SOJ
Modify the given structure to draw the major product(s). Use the single bond tool to interconvert between double and single
bonds. If a racemic mixture of enantiomers is expected, draw both enantiomers. Note: you can select a structure and use Copy and
Paste to save drawing time.
CH₂
Edit Drawing
A
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