1. reagent 1 2. reagent 2 3. reagent 3 Br

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Orgo Chmistry II HW need help.

Please explain why I can't switch the order. Why  I cannot make ketone to be the reagent 1 , (Br2, FeBr3) the reagent 2, and( CH2CH3) the reagent 3???? I have answer, but I just do not understand why ketone can't be reagent 1.

Select reagent 1:

- **Option:** CH₃CH₂Cl, AlCl₃

Select reagent 2:

- **Option:** \( \text{ClC(=O)} \), AlCl₃

Select reagent 3:

- **Option:** Br₂, FeBr₃

### Description of Diagrams

This interface displays options for selecting various chemical reagents, likely for an educational exercise on chemical reactions. The reagents listed are commonly used in organic synthesis, specifically in Friedel-Crafts reactions and halogenation.

1. **Reagent 1:** Ethyl chloride (CH₃CH₂Cl) with aluminum chloride (AlCl₃), a catalyst for alkylation reactions.
2. **Reagent 2:** Acyl chloride \( \text{ClC(=O)} \), with aluminum chloride (AlCl₃), for acylation reactions.
3. **Reagent 3:** Bromine (Br₂) with iron(III) bromide (FeBr₃), used for bromination of aromatic compounds. 

These reagents suggest a focus on learning about electrophilic aromatic substitution reactions.
Transcribed Image Text:Select reagent 1: - **Option:** CH₃CH₂Cl, AlCl₃ Select reagent 2: - **Option:** \( \text{ClC(=O)} \), AlCl₃ Select reagent 3: - **Option:** Br₂, FeBr₃ ### Description of Diagrams This interface displays options for selecting various chemical reagents, likely for an educational exercise on chemical reactions. The reagents listed are commonly used in organic synthesis, specifically in Friedel-Crafts reactions and halogenation. 1. **Reagent 1:** Ethyl chloride (CH₃CH₂Cl) with aluminum chloride (AlCl₃), a catalyst for alkylation reactions. 2. **Reagent 2:** Acyl chloride \( \text{ClC(=O)} \), with aluminum chloride (AlCl₃), for acylation reactions. 3. **Reagent 3:** Bromine (Br₂) with iron(III) bromide (FeBr₃), used for bromination of aromatic compounds. These reagents suggest a focus on learning about electrophilic aromatic substitution reactions.
The image depicts a multi-step chemical reaction process involving a benzene ring as the starting material, which is transformed into a substituted benzene derivative. 

### Reaction Overview:

1. **Starting Material:**
   - **Benzene (C₆H₆):** A simple aromatic hydrocarbon represented by a hexagonal ring with alternating double bonds.

2. **Reagents (Sequential):**
   - **Reagent 1**
   - **Reagent 2**
   - **Reagent 3**

These reagents are used in sequence to facilitate the transformation of benzene into the target compound.

3. **Final Product:**
   - The product is a benzene derivative with three specific modifications:
     - An ethyl group \( \text{-CH}_2\text{-CH}_3 \) attached to the benzene ring.
     - A bromine atom \( \text{-Br} \) attached to the benzene ring, indicating bromination.
     - A ketone group \( \text{-C=O} \) attached to the ethyl group, forming an acyle benzene, specifically with the structure resembling acetophenone.

### Structural Features:

- The final compound retains the aromatic benzene ring structure.
- Substituents on the benzene ring are positioned such that the bromine and ketone functionalities are ortho-substituted relative to each other.

### Diagram Explanation:

The diagram delineates the conversion pathway from benzene to the final aromatic compound, using three unspecified reagents to perform the necessary chemical transformations. This showcases a typical example of functional group transformations in organic chemistry, demonstrating how a simple aromatic molecule can be converted into a more complex substituted aromatic compound.
Transcribed Image Text:The image depicts a multi-step chemical reaction process involving a benzene ring as the starting material, which is transformed into a substituted benzene derivative. ### Reaction Overview: 1. **Starting Material:** - **Benzene (C₆H₆):** A simple aromatic hydrocarbon represented by a hexagonal ring with alternating double bonds. 2. **Reagents (Sequential):** - **Reagent 1** - **Reagent 2** - **Reagent 3** These reagents are used in sequence to facilitate the transformation of benzene into the target compound. 3. **Final Product:** - The product is a benzene derivative with three specific modifications: - An ethyl group \( \text{-CH}_2\text{-CH}_3 \) attached to the benzene ring. - A bromine atom \( \text{-Br} \) attached to the benzene ring, indicating bromination. - A ketone group \( \text{-C=O} \) attached to the ethyl group, forming an acyle benzene, specifically with the structure resembling acetophenone. ### Structural Features: - The final compound retains the aromatic benzene ring structure. - Substituents on the benzene ring are positioned such that the bromine and ketone functionalities are ortho-substituted relative to each other. ### Diagram Explanation: The diagram delineates the conversion pathway from benzene to the final aromatic compound, using three unspecified reagents to perform the necessary chemical transformations. This showcases a typical example of functional group transformations in organic chemistry, demonstrating how a simple aromatic molecule can be converted into a more complex substituted aromatic compound.
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