MECHANISMS 1,2-epoxy-1-methylcyclopentane undergoes both acid-catalyzed and base-catalyzed opening of the epoxide ring to form two different products. > Using ethanol as the solvent and an appropriate acid, show the steps in the acid catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). >Using ethanol as the solvent and an appropriate base, show the steps in the base- catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s).
MECHANISMS 1,2-epoxy-1-methylcyclopentane undergoes both acid-catalyzed and base-catalyzed opening of the epoxide ring to form two different products. > Using ethanol as the solvent and an appropriate acid, show the steps in the acid catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s). >Using ethanol as the solvent and an appropriate base, show the steps in the base- catalyzed mechanism, writing structures for all products of the steps. Circle the major product(s).
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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
Transcribed Image Text:МЕСНANISMS
1,2-epoxy-1-methylcyclopentane undergoes both acid-catalyzed and base-catalyzed
opening of the epoxide ring to form two different products.
> Using ethanol as the solvent and an appropriate acid, show the steps in the acid
catalyzed mechanism, writing structures for all products of the steps. Circle the major
product(s).
> Using ethanol as the solvent and an appropriate base, show the steps in the base-
catalyzed mechanism, writing structures for all products of the steps. Circle the major
product(s).
1,2-epoxy-1-methylcyclopentane
CH3
Expert Solution
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Step 1
Epoxides shows SN1 type ring opening reactions when treated in acidic medium whereas they shows SN1 type in basic medium.
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