CH3OH H2SO4

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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Draw the major product formed in the reaction of an epoxide with acidic methanol.

The image depicts a chemical reaction involving a compound on the left with an epoxide ring, indicated by an oxygen atom (O) bonded to two carbon atoms, forming a three-membered ring structure. This compound features two methyl groups (CH₃) attached to the adjacent carbon of the epoxide.

To the right of the epoxide is the reaction conditions: methanol (CH₃OH) and sulfuric acid (H₂SO₄). An arrow indicates the progression of the reaction from the epoxide to an unspecified product.

This reaction likely involves the opening of the epoxide ring, facilitated by the acidic environment created by sulfuric acid, with methanol acting as a nucleophile.
Transcribed Image Text:The image depicts a chemical reaction involving a compound on the left with an epoxide ring, indicated by an oxygen atom (O) bonded to two carbon atoms, forming a three-membered ring structure. This compound features two methyl groups (CH₃) attached to the adjacent carbon of the epoxide. To the right of the epoxide is the reaction conditions: methanol (CH₃OH) and sulfuric acid (H₂SO₄). An arrow indicates the progression of the reaction from the epoxide to an unspecified product. This reaction likely involves the opening of the epoxide ring, facilitated by the acidic environment created by sulfuric acid, with methanol acting as a nucleophile.
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