Predict the major otherwise, ex = excess. a) The product on the right is made by renating the aldehyde wo/ the will also be made CH₂ = PPMs; verify your answer by by confirming that the same product the four steps shown. final organic product (s). Reactant ratio 1. KM04,4 2. CHyLilox) 3-71₂0*(x) -CH CH₂=PPh 3 06 1. CH₂ Mg Br 2. H₂0 3. PB3 4. KOC(CH3)3 is Il unless stated

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Predict the product
**Title: Predicting Major Organic Product(s) from Reactant Ratios**

**Objective:**
Determine the major final organic product(s) when given reactant ratios of 1:1 unless otherwise stated (ex = excess).

**Exercise:**

a) **Task:**
Verify that the product on the right, produced by reacting the aldehyde with the specific reagents, is consistent with the product formed through the four procedural steps indicated. 

**Reaction Details:**

- **Starting Compound:**
  - Cyclohexanecarboxaldehyde

- **Reagents and Steps:**
  1. **KMnO₄ (aq)**
  2. **CH₂Li (excess)**
  3. **H₃O⁺**
 
**Alternate Reaction Path:**

- **Target Compound Formation:**
  - CH₂=PPh₃ 
  - or 
  - 1. CH₃MgBr
  - 2. H₂O
  - 3. PBr₃
  - 4. KOCH₃

**Explanation of Diagram:**
The diagram illustrates the cyclohexanecarboxaldehyde undergoing transformations through a series of chemical reactions. The left side depicts the initial molecule, and the sequence of reagents is indicated below it. A phosphonium ylide (CH₂=PPh₃) is involved in creating the Wittig reaction, converting an aldehyde into an alkene. Each step in the reaction sequence is designed to alter the structure, ultimately proving that both methods yield the same product.

**Conclusion:**
Students should confirm the transformations based on the given steps to affirm that each pathway achieves the target molecule identically, practicing prediction of reaction outcomes in synthetic organic chemistry.
Transcribed Image Text:**Title: Predicting Major Organic Product(s) from Reactant Ratios** **Objective:** Determine the major final organic product(s) when given reactant ratios of 1:1 unless otherwise stated (ex = excess). **Exercise:** a) **Task:** Verify that the product on the right, produced by reacting the aldehyde with the specific reagents, is consistent with the product formed through the four procedural steps indicated. **Reaction Details:** - **Starting Compound:** - Cyclohexanecarboxaldehyde - **Reagents and Steps:** 1. **KMnO₄ (aq)** 2. **CH₂Li (excess)** 3. **H₃O⁺** **Alternate Reaction Path:** - **Target Compound Formation:** - CH₂=PPh₃ - or - 1. CH₃MgBr - 2. H₂O - 3. PBr₃ - 4. KOCH₃ **Explanation of Diagram:** The diagram illustrates the cyclohexanecarboxaldehyde undergoing transformations through a series of chemical reactions. The left side depicts the initial molecule, and the sequence of reagents is indicated below it. A phosphonium ylide (CH₂=PPh₃) is involved in creating the Wittig reaction, converting an aldehyde into an alkene. Each step in the reaction sequence is designed to alter the structure, ultimately proving that both methods yield the same product. **Conclusion:** Students should confirm the transformations based on the given steps to affirm that each pathway achieves the target molecule identically, practicing prediction of reaction outcomes in synthetic organic chemistry.
Expert Solution
Step 1: Interpretation of given problem

Given reactant is aldehyde.

CH2=PPh3 is phosphorus ylide and used for Wittig reaction. 

In Wittig reaction aldehydes and ketones are converted into corresponding alkene.


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