1. Circle all the stereocenters in the molecule below then answer the questions that follow (3) Br O (a) how many stereocenters are present? (b) how many possible stereoisomers are there? SH LOH

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**Exercise: Stereochemistry in Organic Molecules**

1. **Task**: Circle all the stereocenters in the molecule below, then answer the questions that follow (3).

   ![Molecular structure](image)

   **Molecule Features**:
   - The molecule has a cyclic backbone with various functional groups attached.
   - Bromine (Br), a ketone (O), a thiol (SH), and a hydroxyl group (OH) are present.

2. **Questions**:

   (a) **How many stereocenters are present?**  
   Answer: __________

   (b) **How many possible stereoisomers are there?**  
   Answer: __________

---

**Review**: Stereocenters are atoms in a molecule bonded to four different substituents, causing stereoisomerism. Each stereocenter can give rise to two different configurations (R or S), doubling the potential number of stereoisomers for every new stereocenter present.

**Note**: Examine the spatial arrangement to identify stereocenters, crucial for understanding the molecule's 3D configuration and potential biological activity.
Transcribed Image Text:**Exercise: Stereochemistry in Organic Molecules** 1. **Task**: Circle all the stereocenters in the molecule below, then answer the questions that follow (3). ![Molecular structure](image) **Molecule Features**: - The molecule has a cyclic backbone with various functional groups attached. - Bromine (Br), a ketone (O), a thiol (SH), and a hydroxyl group (OH) are present. 2. **Questions**: (a) **How many stereocenters are present?** Answer: __________ (b) **How many possible stereoisomers are there?** Answer: __________ --- **Review**: Stereocenters are atoms in a molecule bonded to four different substituents, causing stereoisomerism. Each stereocenter can give rise to two different configurations (R or S), doubling the potential number of stereoisomers for every new stereocenter present. **Note**: Examine the spatial arrangement to identify stereocenters, crucial for understanding the molecule's 3D configuration and potential biological activity.
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