4) Provide a Type 2 reaction and mechanism where a trans product is produced where a ketone is formed

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Type 2 electrophilic addition reaction
### Organic Chemistry: Type 2 Reactions

**Objective:**

1. **Provide a Type 2 reaction and mechanism:**
   - Where a trans product is produced.
   
2. **Provide a Type 2 reaction and mechanism:**
   - Where a ketone is formed.

### Explanation:

Type 2 reactions often involve specific mechanisms where particular stereochemistry or specific functional groups like ketones are formed. The tasks specified require selecting appropriate reactions that can be explored in a typical organic chemistry curriculum.

### Examples and Mechanisms:

1. **Trans Product Formation:**
   - Select a reaction such as an E2 elimination where the mechanism results in a trans-alkene as the major product. Highlight the role of the stereochemistry of the leaving groups and the conditions that favor trans over cis products, such as the use of bulky bases.

2. **Ketone Formation:**
   - Consider reactions like oxidation of secondary alcohols using reagents like PCC (Pyridinium chlorochromate) or Jones oxidation. Describe the step-by-step mechanism of how a secondary alcohol transforms into a ketone, emphasizing the changes in oxidation states and the role of the oxidizing agent.

These descriptions provide a foundational understanding of these chemical processes, which are crucial for students studying organic chemistry.
Transcribed Image Text:### Organic Chemistry: Type 2 Reactions **Objective:** 1. **Provide a Type 2 reaction and mechanism:** - Where a trans product is produced. 2. **Provide a Type 2 reaction and mechanism:** - Where a ketone is formed. ### Explanation: Type 2 reactions often involve specific mechanisms where particular stereochemistry or specific functional groups like ketones are formed. The tasks specified require selecting appropriate reactions that can be explored in a typical organic chemistry curriculum. ### Examples and Mechanisms: 1. **Trans Product Formation:** - Select a reaction such as an E2 elimination where the mechanism results in a trans-alkene as the major product. Highlight the role of the stereochemistry of the leaving groups and the conditions that favor trans over cis products, such as the use of bulky bases. 2. **Ketone Formation:** - Consider reactions like oxidation of secondary alcohols using reagents like PCC (Pyridinium chlorochromate) or Jones oxidation. Describe the step-by-step mechanism of how a secondary alcohol transforms into a ketone, emphasizing the changes in oxidation states and the role of the oxidizing agent. These descriptions provide a foundational understanding of these chemical processes, which are crucial for students studying organic chemistry.
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