1. Write the products of the following reactions. If there is no reaction write NR. For full credit clearly indicate cis or trans relationships in cyclic compounds, where appropriate. h) 1) IID-T IIr 21 HDOH NaOH va ter sclvent CH 1) H,B THF 2) HOOH, NAOH water solvent j) CH 1) H B-THF 2) НООН, N:Oн water solvent
1. Write the products of the following reactions. If there is no reaction write NR. For full credit clearly indicate cis or trans relationships in cyclic compounds, where appropriate. h) 1) IID-T IIr 21 HDOH NaOH va ter sclvent CH 1) H,B THF 2) HOOH, NAOH water solvent j) CH 1) H B-THF 2) НООН, N:Oн water solvent
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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![**Note these acronyms:**
- HOAc = Acetic Acid
- NaOAc = Sodium Acetate
- THF = Tetrahydrofuran
- Ph = Phenyl = C₆H₅
- DMSO = Dimethyl Sulfoxide
- H₃C-O-H = Methanol
- Zn = Zinc
- D = Heavy Hydrogen (1 proton and 1 neutron)
**Chemical Structures:**
- Acetone: \[ \text{H}_3\text{C-C=O-CH}_3 \]
- Acetic Acid: \[ \text{H}_3\text{C-C=O-OH} \]
- THF: \[ \text{Tetrahydrofuran} \]
- Ph: \[ \text{Phenyl (C}_6\text{H}_5) \]
**Instructions:**
1. **Write the products of the following reactions.**
- If there is no reaction, write NR.
- For full credit, clearly indicate cis or trans relationships in cyclic compounds, where appropriate.
**Reactions:**
**h)**
1) \[ \text{DIB-THF} \]
2) \[ \text{HOOH, NaOH} \]
- **Solvent:** Water
**i)**
1) \[ \text{H}_3\text{B, THF} \]
2) \[ \text{HOOH, NaOH} \]
- **Solvent:** Water
**j)**
1) \[ \text{H}_3\text{B-THF} \]
2) \[ \text{HOOH, NaOH} \]
- **Solvent:** Water
**k)**
1) \[ \text{O}_3^\text{uv} \]
2) \[ (\text{CH}_3)_2\text{S} \]
These reactions generally depict hydroboration-oxidation or ozonolysis processes, typically used to convert alkenes to alcohols or cleave double bonds, respectively.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F0b2d8d84-896e-4f9e-963b-da7844b9b0f5%2F3b484fa7-9dcd-47af-85e9-9a819ed4014b%2F0el24md_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Note these acronyms:**
- HOAc = Acetic Acid
- NaOAc = Sodium Acetate
- THF = Tetrahydrofuran
- Ph = Phenyl = C₆H₅
- DMSO = Dimethyl Sulfoxide
- H₃C-O-H = Methanol
- Zn = Zinc
- D = Heavy Hydrogen (1 proton and 1 neutron)
**Chemical Structures:**
- Acetone: \[ \text{H}_3\text{C-C=O-CH}_3 \]
- Acetic Acid: \[ \text{H}_3\text{C-C=O-OH} \]
- THF: \[ \text{Tetrahydrofuran} \]
- Ph: \[ \text{Phenyl (C}_6\text{H}_5) \]
**Instructions:**
1. **Write the products of the following reactions.**
- If there is no reaction, write NR.
- For full credit, clearly indicate cis or trans relationships in cyclic compounds, where appropriate.
**Reactions:**
**h)**
1) \[ \text{DIB-THF} \]
2) \[ \text{HOOH, NaOH} \]
- **Solvent:** Water
**i)**
1) \[ \text{H}_3\text{B, THF} \]
2) \[ \text{HOOH, NaOH} \]
- **Solvent:** Water
**j)**
1) \[ \text{H}_3\text{B-THF} \]
2) \[ \text{HOOH, NaOH} \]
- **Solvent:** Water
**k)**
1) \[ \text{O}_3^\text{uv} \]
2) \[ (\text{CH}_3)_2\text{S} \]
These reactions generally depict hydroboration-oxidation or ozonolysis processes, typically used to convert alkenes to alcohols or cleave double bonds, respectively.
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