1. excess KNH2, heat 2. O3 3. Н-О CI CI. 1. NaNH2 2. isobutyl iodide 3. На, Pt 1.9-BBN 2. HаОг, NaOн

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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**Learning Target 15**

**Criteria for satisfactory score:**

Reactants, products, and reagents that complete a reaction scheme must specify compounds, not generic categories. Reagents and structures must be valid Lewis structures.

**Tasks:**

Complete the synthetic sequences by drawing products/substrates/reagents in the empty spaces in the reactions below.

**Reaction Schemes:**

1. **First Reaction:**
   - Starting compound: Cyclohexane with a chlorine substituent (Cl).
   - Reagents:
     1. Excess KNH₂, heat
     2. O₃
     3. H₂O
   - Diagram indicates an arrow pointing to an unspecified product.

2. **Second Reaction:**
   - Starting compound: An alkyne with a phenyl group (aromatic ring).
   - Reagents:
     1. 9-BBN
     2. H₂O₂, NaOH
   - Diagram indicates an arrow pointing to an unspecified product.

3. **Third Reaction:**
   - Reactants:
     1. Lithium acetylide, DMSO (Sₙ2)
     2. HgSO₄, H₂SO₄, H₂O
   - Product shown: Phenol with a ketone (acetophenone).

4. **Fourth Reaction:**
   - Starting compound: An alkene with tert-butyl groups on each side. 
   - Diagram indicates arrows pointing toward unspecified products and subsequently to a final product with added carbon chains.

**Figure 13: Reactions**
Transcribed Image Text:**Learning Target 15** **Criteria for satisfactory score:** Reactants, products, and reagents that complete a reaction scheme must specify compounds, not generic categories. Reagents and structures must be valid Lewis structures. **Tasks:** Complete the synthetic sequences by drawing products/substrates/reagents in the empty spaces in the reactions below. **Reaction Schemes:** 1. **First Reaction:** - Starting compound: Cyclohexane with a chlorine substituent (Cl). - Reagents: 1. Excess KNH₂, heat 2. O₃ 3. H₂O - Diagram indicates an arrow pointing to an unspecified product. 2. **Second Reaction:** - Starting compound: An alkyne with a phenyl group (aromatic ring). - Reagents: 1. 9-BBN 2. H₂O₂, NaOH - Diagram indicates an arrow pointing to an unspecified product. 3. **Third Reaction:** - Reactants: 1. Lithium acetylide, DMSO (Sₙ2) 2. HgSO₄, H₂SO₄, H₂O - Product shown: Phenol with a ketone (acetophenone). 4. **Fourth Reaction:** - Starting compound: An alkene with tert-butyl groups on each side. - Diagram indicates arrows pointing toward unspecified products and subsequently to a final product with added carbon chains. **Figure 13: Reactions**
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