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). Acetone = Acetic Acid = THF= Ph= H3C CH3 H3C HO, 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. i) 1) H,B THF 2) HOOH, NAOH water solven j) CH 1)H B-THF 2) HOOH, N¿OH water solvent k) 1) O zoue 2) (CH ),S I) CH3 1) Ozcne 2) CH,)S %3D

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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**Educational Resource: Understanding Organic Chemistry Reactions**

### Important 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:

1. **Acetone**: 
   - Structure: \( \text{H}_3\text{C-CO-CH}_3 \)
   
2. **Acetic Acid**: 
   - Structure: \( \text{H}_3\text{C-COOH} \)
   
3. **THF (Tetrahydrofuran)**: 
   - Structure: A cyclic ether with the formula \( \text{C}_4\text{H}_8\text{O} \).
   
4. **Ph (Phenyl)**: 
   - Structure: The phenyl group is represented as a benzene ring, \( \text{C}_6\text{H}_5 \).

### Reaction Exercise:

**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:

- **i)** 
  - Reactant: Cyclohexene compound with a methyl group
  - Reagents: 
    1) \( \text{H}_3\text{B}\), THF 
    2) \( \text{HOOH, NaOH} \), water solvent
   
- **j)** 
  - Reactant: Cyclohexene compound with a methyl group on a different position
  - Reagents: 
    1) \( \text{H}_3\text{B}\), THF
    2) \( \text{HOOH, NaOH} \), water solvent

- **k)**
  - Reactant: A linear alkene with a methyl group
  - Reagents:
    1) Ozone
    2) \( (\text{CH}_3)_2\text{S} \)

-
Transcribed Image Text:**Educational Resource: Understanding Organic Chemistry Reactions** ### Important 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: 1. **Acetone**: - Structure: \( \text{H}_3\text{C-CO-CH}_3 \) 2. **Acetic Acid**: - Structure: \( \text{H}_3\text{C-COOH} \) 3. **THF (Tetrahydrofuran)**: - Structure: A cyclic ether with the formula \( \text{C}_4\text{H}_8\text{O} \). 4. **Ph (Phenyl)**: - Structure: The phenyl group is represented as a benzene ring, \( \text{C}_6\text{H}_5 \). ### Reaction Exercise: **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: - **i)** - Reactant: Cyclohexene compound with a methyl group - Reagents: 1) \( \text{H}_3\text{B}\), THF 2) \( \text{HOOH, NaOH} \), water solvent - **j)** - Reactant: Cyclohexene compound with a methyl group on a different position - Reagents: 1) \( \text{H}_3\text{B}\), THF 2) \( \text{HOOH, NaOH} \), water solvent - **k)** - Reactant: A linear alkene with a methyl group - Reagents: 1) Ozone 2) \( (\text{CH}_3)_2\text{S} \) -
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  • Hydroboration - oxidation reaction
  • Ozonolysis

 

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