For the molecule below: 1. Identify all CHIRAL centers if any are present: 2. Name each CHIRAL center (R or S if they exist):

Chemistry
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Chapter1: Chemical Foundations
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For the molecule below:

1. Identify all CHIRAL centers if any are present.
2. Name each CHIRAL center (R or S if they exist).

**Molecular Structure:**
The diagram shows a cyclohexane ring with two wedge bonds indicating substituents at the top and bottom positions, implying possible chiral centers.

**Options:**

- **A:** NO chiral centers
- **B:** One chiral center: **R**
- **C:** One chiral center: **S**
- **D:** Two chiral centers: (top) **R** and (bottom) **S**
- **E:** Two chiral centers: both **RR**
- **F:** Two chiral centers: (top) **S** and (bottom) **R**
- **G:** Two chiral centers: both **SS**

**Choices:**
- ○ A
- ○ B
- ○ C
- ○ D
- ○ E
- ○ F
- ○ G

This question tests the ability to identify and assign configurations to chiral centers within a molecule. Chiral centers are stereocenters where the spatial arrangement of atoms can lead to non-superimposable mirror images, known as enantiomers. The R/S labels correspond to the Cahn-Ingold-Prelog priority rules used in stereochemistry.
Transcribed Image Text:For the molecule below: 1. Identify all CHIRAL centers if any are present. 2. Name each CHIRAL center (R or S if they exist). **Molecular Structure:** The diagram shows a cyclohexane ring with two wedge bonds indicating substituents at the top and bottom positions, implying possible chiral centers. **Options:** - **A:** NO chiral centers - **B:** One chiral center: **R** - **C:** One chiral center: **S** - **D:** Two chiral centers: (top) **R** and (bottom) **S** - **E:** Two chiral centers: both **RR** - **F:** Two chiral centers: (top) **S** and (bottom) **R** - **G:** Two chiral centers: both **SS** **Choices:** - ○ A - ○ B - ○ C - ○ D - ○ E - ○ F - ○ G This question tests the ability to identify and assign configurations to chiral centers within a molecule. Chiral centers are stereocenters where the spatial arrangement of atoms can lead to non-superimposable mirror images, known as enantiomers. The R/S labels correspond to the Cahn-Ingold-Prelog priority rules used in stereochemistry.
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