Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table. H ***** OH CI Molecule 1 C H 0 Molecule 4 OH ****** H OH 0 CI Unone of the above Molecule 2 Br HO H 0 Molecule 5 Br OH O ***** H Molecule 3 H **** CI OH Molecule 6 CI ***H "Η OH 0 X 5 FEED olo Ar B

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Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of the above box under the table
### Enantiomer Identification Exercise

**Instructions:**  
Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the "none of the above" box under the table.

**Target Molecule:**  
- Structure composed of a central carbon atom bonded to a hydrogen (H), hydroxyl (OH), and chlorine (Cl). The stereochemistry suggests spatial arrangement, indicating potential chirality.

**Molecule Structures for Comparison:**

1. **Molecule 1:**
   - Central carbon with bonds to H, OH at solid wedges/outward, and Cl.

2. **Molecule 2:**
   - Central carbon with bonds to H, Br, and HO.

3. **Molecule 3:**
   - Central carbon with bonds to H, OH, and Cl. Hydroxyl and chlorine have specific spatial orientation with directional wedges.

4. **Molecule 4:**
   - Central carbon with OH, Cl at different spatial orientations.

5. **Molecule 5:**
   - Central carbon with OH, Br, different orientation resembling Molecule 2.

6. **Molecule 6:**
   - Central carbon with Cl, H, OH in reversed spatial configuration as compared to the target.

**Select none of the above** if none match the enantiomeric nature of the target molecule.

---
Utilize the "Explanation" and "Check" buttons for assistance and to validate your selection.
Transcribed Image Text:### Enantiomer Identification Exercise **Instructions:** Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the "none of the above" box under the table. **Target Molecule:** - Structure composed of a central carbon atom bonded to a hydrogen (H), hydroxyl (OH), and chlorine (Cl). The stereochemistry suggests spatial arrangement, indicating potential chirality. **Molecule Structures for Comparison:** 1. **Molecule 1:** - Central carbon with bonds to H, OH at solid wedges/outward, and Cl. 2. **Molecule 2:** - Central carbon with bonds to H, Br, and HO. 3. **Molecule 3:** - Central carbon with bonds to H, OH, and Cl. Hydroxyl and chlorine have specific spatial orientation with directional wedges. 4. **Molecule 4:** - Central carbon with OH, Cl at different spatial orientations. 5. **Molecule 5:** - Central carbon with OH, Br, different orientation resembling Molecule 2. 6. **Molecule 6:** - Central carbon with Cl, H, OH in reversed spatial configuration as compared to the target. **Select none of the above** if none match the enantiomeric nature of the target molecule. --- Utilize the "Explanation" and "Check" buttons for assistance and to validate your selection.
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