Br. ОН CH3 CH3 H3C ОН H*, remove water Br. CH3 H3C CH3 1) Mg/ether 2) CH,CH=O 3) H2O+

Chemistry
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Chapter1: Chemical Foundations
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What’s the final product? And what functional group was created in the first step?
The image depicts a chemical reaction sequence involving organic compounds.

### Initial Reactants:
1. **Reactant 1**: A bromobenzene derivative with the structure:
   - A benzene ring (aromatic ring) attached to a bromine (Br) atom.
   - Connected to a side chain with a CH₃ group, a hydroxyl group (OH), and a secondary alcohol (CHOH) group.
2. **Reactant 2**: A ketone with the structure:
   - Acetone (CH₃-C(=O)-CH₃).

### Reaction Process:
- **Step 1**: The first stage involves acid-catalyzed removal of water using an acid (H⁺) to form an intermediate compound.
- **Intermediate Product**: This intermediate is a cyclic ether with a five-membered ring including ketone functionality and bromine substituent on the benzene ring.

### Further Reaction Sequence:
1. **Step 1**: The intermediate reacts with magnesium in ether solvent, forming a Grignard reagent.
2. **Step 2**: The Grignard reagent then reacts with ethanal (acetaldehyde, CH₃CHO).
3. **Step 3**: Acidic workup with H₃O⁺ (hydronium ion) completes the reaction, yielding the final product.

### Diagram Explanation:
- **Left Part**: Reactants are shown with structural formulas.
- **Middle Arrow**: Indicates reaction conditions and directional progress through an aqueous environment under acidic conditions.
- **Right Part**: Displays the formation of an intermediate compound with further steps annotated on the side.

These steps demonstrate typical organic synthesis and reaction mechanisms involving aromatic compounds and the formation of Grignard reagents, commonly studied in organic chemistry courses.
Transcribed Image Text:The image depicts a chemical reaction sequence involving organic compounds. ### Initial Reactants: 1. **Reactant 1**: A bromobenzene derivative with the structure: - A benzene ring (aromatic ring) attached to a bromine (Br) atom. - Connected to a side chain with a CH₃ group, a hydroxyl group (OH), and a secondary alcohol (CHOH) group. 2. **Reactant 2**: A ketone with the structure: - Acetone (CH₃-C(=O)-CH₃). ### Reaction Process: - **Step 1**: The first stage involves acid-catalyzed removal of water using an acid (H⁺) to form an intermediate compound. - **Intermediate Product**: This intermediate is a cyclic ether with a five-membered ring including ketone functionality and bromine substituent on the benzene ring. ### Further Reaction Sequence: 1. **Step 1**: The intermediate reacts with magnesium in ether solvent, forming a Grignard reagent. 2. **Step 2**: The Grignard reagent then reacts with ethanal (acetaldehyde, CH₃CHO). 3. **Step 3**: Acidic workup with H₃O⁺ (hydronium ion) completes the reaction, yielding the final product. ### Diagram Explanation: - **Left Part**: Reactants are shown with structural formulas. - **Middle Arrow**: Indicates reaction conditions and directional progress through an aqueous environment under acidic conditions. - **Right Part**: Displays the formation of an intermediate compound with further steps annotated on the side. These steps demonstrate typical organic synthesis and reaction mechanisms involving aromatic compounds and the formation of Grignard reagents, commonly studied in organic chemistry courses.
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