Can you further explain c & d? I'm confused with both as those were the only ones I got wrong. First for c, why is there a reaction on the most substituted alkene vs the terminal alkene? Secondly for d, why did both OH groups experience a reaction vs just the attached to a primary carbon. Thank youagain for the help!

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Can you further explain c & d? I'm confused with both as those were the only ones I got wrong. First for c, why is there a reaction on the most substituted alkene vs the terminal alkene? Secondly for d, why did both OH groups experience a reaction vs just the attached to a primary carbon. Thank youagain for the help!

### Chemical Reactions and Mechanisms

#### Example c.
**Reactants and Conditions**:
- **Reactant**: An unsaturated hydrocarbon containing three carbon-carbon double bonds (1,5-Hexadiene).
- **Reagent**: PhCO₃H (perbenzoic acid) with CH₂Cl₂ as the solvent.

**Reaction and Product**:
- This represents an epoxidation reaction where the perbenzoic acid forms an epoxide ring at one of the double bonds.
- **Product**: A compound with an epoxide ring and two remaining double bonds.

#### Example d.
**Reactants and Conditions**:
- **Reactant**: A diol (specifically, 1,2-Butanediol).
- **Reagent**: CrO₃ in H₂SO₄, a common reagent for oxidation reactions.

**Reaction and Product**:
- This signifies a Jones oxidation process wherein the secondary alcohol (-OH) group is oxidized to a ketone (C=O), while the primary alcohol remains unchanged.
- **Product**: A compound with a ketone group and a remaining hydroxyl group.

### Diagrams Explanation
The diagrams illustrate the chemical structures before and after the reactions.

1. **First Diagram (Example c)**
   - **Left Side**: The starting material is 1,5-Hexadiene, a chain of six carbon atoms with three alternating double bonds.
   - **Right Side**: The product shows the formation of an epoxide ring on the second double bond (forming a three-membered oxygen-containing ring), while retaining the other two double bonds.

2. **Second Diagram (Example d)**
   - **Left Side**: The starting material is 1,2-Butanediol, a four-carbon chain with hydroxyl groups on the first and second carbon atoms.
   - **Right Side**: The product displays a ketone group (carbon-oxygen double bond) on the second carbon and a hydroxyl group remaining on the first carbon.

These diagrams and the associated reactions are crucial for understanding organic reaction mechanisms, particularly epoxidation and oxidation processes.
Transcribed Image Text:### Chemical Reactions and Mechanisms #### Example c. **Reactants and Conditions**: - **Reactant**: An unsaturated hydrocarbon containing three carbon-carbon double bonds (1,5-Hexadiene). - **Reagent**: PhCO₃H (perbenzoic acid) with CH₂Cl₂ as the solvent. **Reaction and Product**: - This represents an epoxidation reaction where the perbenzoic acid forms an epoxide ring at one of the double bonds. - **Product**: A compound with an epoxide ring and two remaining double bonds. #### Example d. **Reactants and Conditions**: - **Reactant**: A diol (specifically, 1,2-Butanediol). - **Reagent**: CrO₃ in H₂SO₄, a common reagent for oxidation reactions. **Reaction and Product**: - This signifies a Jones oxidation process wherein the secondary alcohol (-OH) group is oxidized to a ketone (C=O), while the primary alcohol remains unchanged. - **Product**: A compound with a ketone group and a remaining hydroxyl group. ### Diagrams Explanation The diagrams illustrate the chemical structures before and after the reactions. 1. **First Diagram (Example c)** - **Left Side**: The starting material is 1,5-Hexadiene, a chain of six carbon atoms with three alternating double bonds. - **Right Side**: The product shows the formation of an epoxide ring on the second double bond (forming a three-membered oxygen-containing ring), while retaining the other two double bonds. 2. **Second Diagram (Example d)** - **Left Side**: The starting material is 1,2-Butanediol, a four-carbon chain with hydroxyl groups on the first and second carbon atoms. - **Right Side**: The product displays a ketone group (carbon-oxygen double bond) on the second carbon and a hydroxyl group remaining on the first carbon. These diagrams and the associated reactions are crucial for understanding organic reaction mechanisms, particularly epoxidation and oxidation processes.
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