### Exercise 3: Naming Organic Structures**Task**: Provide an IUPAC name for the structures below. Pay attention to absolute stereochemistry.#### Structure Descriptions1. **Left Structure:** - **Type**: Cyclohexane ring - **Substituents**: - **Chlorine (Cl)**: Two chlorine atoms attached to adjacent carbon atoms. - **Hydroxyl group (OH)**: Attached to a carbon atom distinct from the ones bonded to chlorine. - **Stereochemistry**: - The chlorine atoms and the hydroxyl group are depicted with wedges, indicating specific stereochemical configurations (bold for upward, dashed for downward).2. **Right Structure:** - **Type**: Linear chain - **Substituents**: - **Hydroxyl group (OH)**: Attached to the second carbon in the chain. - **Chlorine (Cl)**: Attached to the penultimate carbon in the chain. - **Stereochemistry**: - The hydroxyl group shows stereochemistry, indicated by a wedged bond.When providing the IUPAC names, ensure that absolute stereochemistry (R/S notation) is used to accurately describe the spatial arrangement of the substituents on the chiral centers.

Answered: 3. Provide an IUPAC name for the…

3. Provide an IUPAC name for the structures below. Pay attention to absolute stereochemistr CI HO, OH CI

10th Edition

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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