On the propane skeleton below, drawn in the necessary substituents using wedge and dash notation to produce the structure (S) – 1-bromo-1-chloropropane.

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**Question 5:**

On the propane skeleton below, draw in the necessary substituents using wedge and dash notation to produce the structure (S)-1-bromo-1-chloropropane.

**Diagram Explanation:**

The diagram shows a simplified skeletal structure of propane. It includes:

- A central carbon atom connected to a hydrogen atom (H) depicted by a small "H" attached to one bond.
- Three bonds are extending from the central carbon atom, indicating the possible attachment points for additional atoms or groups.
- The task requires adding bromine (Br) and chlorine (Cl) substituents to this propane skeleton using wedge-and-dash notation, which indicates the three-dimensional spatial arrangement of the atoms.

In wedge-and-dash notation:

- Solid wedge bonds indicate that the bond is coming out of the plane, towards the viewer.
- Dash bonds indicate that the bond is going into the plane, away from the viewer.

The goal is to create the (S)-1-bromo-1-chloropropane configuration, which involves specific stereochemistry.
Transcribed Image Text:**Question 5:** On the propane skeleton below, draw in the necessary substituents using wedge and dash notation to produce the structure (S)-1-bromo-1-chloropropane. **Diagram Explanation:** The diagram shows a simplified skeletal structure of propane. It includes: - A central carbon atom connected to a hydrogen atom (H) depicted by a small "H" attached to one bond. - Three bonds are extending from the central carbon atom, indicating the possible attachment points for additional atoms or groups. - The task requires adding bromine (Br) and chlorine (Cl) substituents to this propane skeleton using wedge-and-dash notation, which indicates the three-dimensional spatial arrangement of the atoms. In wedge-and-dash notation: - Solid wedge bonds indicate that the bond is coming out of the plane, towards the viewer. - Dash bonds indicate that the bond is going into the plane, away from the viewer. The goal is to create the (S)-1-bromo-1-chloropropane configuration, which involves specific stereochemistry.
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