There are four different starting molecules that one might use to synthesize the illustrated alkyl halide as the major product using an electrophilic addition reaction. Please draw all four of them.

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There are four different starting molecules that one might use to synthesize the illustrated alkyl halide as the major product using an electrophilic addition reaction. Please draw all four of them.

**Chemical Reaction Analysis**

The image presents a chemical reaction scheme involving an unidentified starting material reacting with hydrobromic acid (HBr) to form a specific organic compound featuring an indane structure with a methyl group (CH₃) and a bromine (Br) atom attached.

**Reaction Details:**

1. **Starting Material:**
   - The starting material is not explicitly defined in the image. It is represented as a question mark (?).

2. **Reagent:**
   - Hydrobromic acid (HBr) is used as a reagent, indicating a possible addition reaction involving bromination.

3. **Product:**
   - The product formed is a brominated indane derivative. The structure indicates a bromine (Br) atom and a methyl group (CH₃) attached to a fused bicyclic aromatic system.

**Possible Structures for Starting Material:**

- The lower portion of the image displays four organic structures that are likely potential candidates for the starting material:

  1. **Structure 1:** A phenyl group attached to a cyclohexene ring.
  2. **Structure 2:** A structure similar to the above, but with an additional alkyl group on the cyclohexene ring.
  3. **Structure 3:** Another variation with different positioning of the phenyl group.
  4. **Structure 4:** Additional phenyl groups attached to the cyclohexene core.

These structures suggest variations in phenyl and alkyl group placement, affecting the final product's configuration after reaction with HBr.

**Summary:**
The image explores different potential starting materials for synthesizing a brominated indane derivative via reaction with hydrobromic acid, emphasizing the influence of structural variations on the final product.
Transcribed Image Text:**Chemical Reaction Analysis** The image presents a chemical reaction scheme involving an unidentified starting material reacting with hydrobromic acid (HBr) to form a specific organic compound featuring an indane structure with a methyl group (CH₃) and a bromine (Br) atom attached. **Reaction Details:** 1. **Starting Material:** - The starting material is not explicitly defined in the image. It is represented as a question mark (?). 2. **Reagent:** - Hydrobromic acid (HBr) is used as a reagent, indicating a possible addition reaction involving bromination. 3. **Product:** - The product formed is a brominated indane derivative. The structure indicates a bromine (Br) atom and a methyl group (CH₃) attached to a fused bicyclic aromatic system. **Possible Structures for Starting Material:** - The lower portion of the image displays four organic structures that are likely potential candidates for the starting material: 1. **Structure 1:** A phenyl group attached to a cyclohexene ring. 2. **Structure 2:** A structure similar to the above, but with an additional alkyl group on the cyclohexene ring. 3. **Structure 3:** Another variation with different positioning of the phenyl group. 4. **Structure 4:** Additional phenyl groups attached to the cyclohexene core. These structures suggest variations in phenyl and alkyl group placement, affecting the final product's configuration after reaction with HBr. **Summary:** The image explores different potential starting materials for synthesizing a brominated indane derivative via reaction with hydrobromic acid, emphasizing the influence of structural variations on the final product.
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