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other NaOMe (1eq) MeOH H+ 용 2. acidic work-up | J

other NaOMe (1eq) MeOH H+ 용 2. acidic work-up | J

Chemistry
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 structures of the major organic product(s) in the following reactions. Each box represents one product. Show stereochemistry of the products, where applicable. 

The image shows two separate chemical reactions, each with its own set of reactants and products. **Reaction I:** - **Reactant:** The given structure is a cyclohexane ring attached to a compound with an amide group (–CONH) and an ester group (–COOCH3). - **Reagent:** Sodium methoxide (NaOMe) in methanol (MeOH). - **Product:** The result of this reaction is not shown and is represented by the letter "I." **Reaction J:** - **Reactants:** 1. The first step involves a cyclopentanone reacting with an imine (shown with a pentagon and H+), indicating an acid-catalyzed cyclization reaction. 2. A subsequent step adds an acetyl group (represented as a two-carbon chain with a chlorine leaving group, Cl). - **Reagent:** This is followed by an acidic work-up. - **Product:** The final product is represented by the letter "J." Both reactions involve complex transformations and indicate areas where further exploration or study would be beneficial for students, particularly in understanding mechanisms or predicting products in organic chemistry.
Transcribed Image Text:The image shows two separate chemical reactions, each with its own set of reactants and products. **Reaction I:** - **Reactant:** The given structure is a cyclohexane ring attached to a compound with an amide group (–CONH) and an ester group (–COOCH3). - **Reagent:** Sodium methoxide (NaOMe) in methanol (MeOH). - **Product:** The result of this reaction is not shown and is represented by the letter "I." **Reaction J:** - **Reactants:** 1. The first step involves a cyclopentanone reacting with an imine (shown with a pentagon and H+), indicating an acid-catalyzed cyclization reaction. 2. A subsequent step adds an acetyl group (represented as a two-carbon chain with a chlorine leaving group, Cl). - **Reagent:** This is followed by an acidic work-up. - **Product:** The final product is represented by the letter "J." Both reactions involve complex transformations and indicate areas where further exploration or study would be beneficial for students, particularly in understanding mechanisms or predicting products in organic chemistry.
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