b) Do either left (bottom) or right (top). If you have time at the end to do both, I will count your best one. Deuterium (D) is just an isotope of hydrogen (H). H₂CH₂CH₂CS NaBD4 CH3OH (ex) SCH₂CH₂CH3 (H₂SO4) H₂O (ex)

Chemistry
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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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**Instructions for Students:**

**Task b**  
You need to complete either the left (bottom) path or the right (top) path. If you finish both, I will evaluate your best submission. Keep in mind that Deuterium (D) is an isotope of hydrogen (H).

**Chemical Reaction Pathways:**

1. **Left Pathway:**
   - Reactants: The molecular structure shown has a cyclohexanone core with substituents including an ethyl group and a thioethoxy group.
   - Reagents: NaBD₄ (Sodium Borodeuteride) and CH₃OH (Methanol, in excess).
   - Process: This pathway likely involves a reduction reaction targeting the carbonyl group.

2. **Right Pathway:**
   - Reactants: Same starting molecular structure as the left pathway.
   - Reagents: (H₂SO₄) and H₂O (in excess).
   - Process: This is possibly an acid-catalyzed hydrolysis or similar transformation involving sulfuric acid.

**Diagram Explanation:**

- The central structure is a cyclohexane ring with a carbonyl group.
- To the left, the reaction conditions involve a reducing agent (NaBD₄) which may reduce the carbonyl to an alcohol.
- To the right, the presence of sulfuric acid suggests an acid-mediated transformation, affecting the substituents or the functional group.

**Note:** When writing your solution, be precise about the reaction mechanisms and the expected products for each pathway.
Transcribed Image Text:**Instructions for Students:** **Task b** You need to complete either the left (bottom) path or the right (top) path. If you finish both, I will evaluate your best submission. Keep in mind that Deuterium (D) is an isotope of hydrogen (H). **Chemical Reaction Pathways:** 1. **Left Pathway:** - Reactants: The molecular structure shown has a cyclohexanone core with substituents including an ethyl group and a thioethoxy group. - Reagents: NaBD₄ (Sodium Borodeuteride) and CH₃OH (Methanol, in excess). - Process: This pathway likely involves a reduction reaction targeting the carbonyl group. 2. **Right Pathway:** - Reactants: Same starting molecular structure as the left pathway. - Reagents: (H₂SO₄) and H₂O (in excess). - Process: This is possibly an acid-catalyzed hydrolysis or similar transformation involving sulfuric acid. **Diagram Explanation:** - The central structure is a cyclohexane ring with a carbonyl group. - To the left, the reaction conditions involve a reducing agent (NaBD₄) which may reduce the carbonyl to an alcohol. - To the right, the presence of sulfuric acid suggests an acid-mediated transformation, affecting the substituents or the functional group. **Note:** When writing your solution, be precise about the reaction mechanisms and the expected products for each pathway.
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