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1. panisole Grignard 2. 5% HCI 4 人 LLIAM E EYON cat. N-SOO

1. panisole Grignard 2. 5% HCI 4 人 LLIAM E EYON cat. N-SOO

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 product for each reaction 

### Organic Chemistry Reactions 1. **Cyclohexanone Reaction:** - **Structure:** Cyclohexanone - **Reagents:** 1. **p-Anisole Grignard** 2. **5% HCl** 2. **α,β-Unsaturated Carbonyl Reaction:** - **Structure:** α,β-Unsaturated carbonyl compound - **Reagents:** 1. **LiAlH₄ in THF** 2. **5% HCl** 3. **Oxidation of Secondary Alcohol:** - **Structure:** Secondary alcohol - **Reagents:** - **CrO₃ in H₂O, then H₂SO₄ and acetone** 4. **Acetophenone Formation:** - **Structure:** Acetophenone - **Reagents:** - **EtOH in the presence of catalytic H₂SO₄** ### Diagram Details: - The provided structures represent organic compounds at various stages of chemical transformations. - Arrows indicate the progression of reactions from starting materials to products. - Reagents are written above or below the arrows, specifying conditions used for each transformation. Understanding these reactions is crucial for mastering advanced concepts in organic synthesis, including nucleophilic addition, reduction, and oxidation.
Transcribed Image Text:### Organic Chemistry Reactions 1. **Cyclohexanone Reaction:** - **Structure:** Cyclohexanone - **Reagents:** 1. **p-Anisole Grignard** 2. **5% HCl** 2. **α,β-Unsaturated Carbonyl Reaction:** - **Structure:** α,β-Unsaturated carbonyl compound - **Reagents:** 1. **LiAlH₄ in THF** 2. **5% HCl** 3. **Oxidation of Secondary Alcohol:** - **Structure:** Secondary alcohol - **Reagents:** - **CrO₃ in H₂O, then H₂SO₄ and acetone** 4. **Acetophenone Formation:** - **Structure:** Acetophenone - **Reagents:** - **EtOH in the presence of catalytic H₂SO₄** ### Diagram Details: - The provided structures represent organic compounds at various stages of chemical transformations. - Arrows indicate the progression of reactions from starting materials to products. - Reagents are written above or below the arrows, specifying conditions used for each transformation. Understanding these reactions is crucial for mastering advanced concepts in organic synthesis, including nucleophilic addition, reduction, and oxidation.
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