The completion of the synthesis of the first compound is provided below. B Br Using the list below, identify the reagent(s) that correspond to each letter in the reaction scheme: Reagent(s) A ✓and Reagent(s) B ✓ Reagent(s) C 1. H₂, Pt 2. NaNH2 3. HC=CNa 4.1) 03; 2) DMS 5. H₂, Lindlar's cat. 6. 1) R₂BH; 2) H₂O2, NaOH 7. HBr, ROOR 8. 1) xs NaNH2; 2) H2O 9. H₂SO4, H₂O, HgSO4
The completion of the synthesis of the first compound is provided below. B Br Using the list below, identify the reagent(s) that correspond to each letter in the reaction scheme: Reagent(s) A ✓and Reagent(s) B ✓ Reagent(s) C 1. H₂, Pt 2. NaNH2 3. HC=CNa 4.1) 03; 2) DMS 5. H₂, Lindlar's cat. 6. 1) R₂BH; 2) H₂O2, NaOH 7. HBr, ROOR 8. 1) xs NaNH2; 2) H2O 9. H₂SO4, H₂O, HgSO4
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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![### Completion of Compound Synthesis
The completion of the synthesis of the first compound is provided below.
![Reaction Scheme](reaction-scheme.png)
### Reaction Scheme Explanation
The image shows a reaction scheme containing a series of compounds and arrows labeled as A, B, and C, leading to the final product.
- **Compound 1:** Starting material includes a long carbon chain with a triple bond.
- **Compound 2 (After Reagent A):** Similar structure but with a bromine atom attached.
- **Compound 3 (After Reagent B):** Further modified with possibly elongation or functionalization.
- **Compound 4 (After Reagent C):** The final product, a ketone with a specified carbon chain.
### Reagent Selection
Using the list below, identify the reagent(s) that correspond to each letter in the reaction scheme:
- **Reagent(s) A:**
- 1. H2, Pt
- 2. NaNH2
- 3. HC≡CNa
- 4. 1) O3; 2) DMS
- 5. H2, Lindlar’s cat.
- 6. 1) R2BH; 2) H2O2, NaOH
- 7. HBr, ROOR
- 8. 1) xs NaNH2; 2) H2O
- 9. H2SO4, H2O, HgSO4
- **Reagent(s) B:**
- 1. H2, Pt
- 2. NaNH2
- 3. HC≡CNa
- 4. 1) O3; 2) DMS
- 5. H2, Lindlar’s cat.
- 6. 1) R2BH; 2) H2O2, NaOH
- 7. HBr, ROOR
- 8. 1) xs NaNH2; 2) H2O
- 9. H2SO4, H2O, HgSO4
- **Reagent(s) C:**
- 1. H2, Pt
- 2. NaNH2
- 3. HC≡CNa
- 4](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F4167b07b-ab2c-42e3-ab89-9f12261de975%2F9bee06ca-a476-4d05-b994-8457046f4bb5%2Fmxyc62_processed.png&w=3840&q=75)
Transcribed Image Text:### Completion of Compound Synthesis
The completion of the synthesis of the first compound is provided below.
![Reaction Scheme](reaction-scheme.png)
### Reaction Scheme Explanation
The image shows a reaction scheme containing a series of compounds and arrows labeled as A, B, and C, leading to the final product.
- **Compound 1:** Starting material includes a long carbon chain with a triple bond.
- **Compound 2 (After Reagent A):** Similar structure but with a bromine atom attached.
- **Compound 3 (After Reagent B):** Further modified with possibly elongation or functionalization.
- **Compound 4 (After Reagent C):** The final product, a ketone with a specified carbon chain.
### Reagent Selection
Using the list below, identify the reagent(s) that correspond to each letter in the reaction scheme:
- **Reagent(s) A:**
- 1. H2, Pt
- 2. NaNH2
- 3. HC≡CNa
- 4. 1) O3; 2) DMS
- 5. H2, Lindlar’s cat.
- 6. 1) R2BH; 2) H2O2, NaOH
- 7. HBr, ROOR
- 8. 1) xs NaNH2; 2) H2O
- 9. H2SO4, H2O, HgSO4
- **Reagent(s) B:**
- 1. H2, Pt
- 2. NaNH2
- 3. HC≡CNa
- 4. 1) O3; 2) DMS
- 5. H2, Lindlar’s cat.
- 6. 1) R2BH; 2) H2O2, NaOH
- 7. HBr, ROOR
- 8. 1) xs NaNH2; 2) H2O
- 9. H2SO4, H2O, HgSO4
- **Reagent(s) C:**
- 1. H2, Pt
- 2. NaNH2
- 3. HC≡CNa
- 4
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