### Assign the Absolute Configuration (R or S) of the Chiral Carbons in the Molecules Below: #### a) The first molecule is a five-membered ring with the following substituents: - A hydroxyl group (OH) attached to the first carbon. - A bromine atom (Br) on the second carbon, with a wedge indicating it projects forward. - A propyl group (CH₂CH₂CH₃) also attached to the second carbon, with a dashed line indicating it projects backward. - A carbonyl group (C=O) on the third carbon. #### b) The second molecule is a carbon chain with multiple functional groups: - A hydroxyl group (OH) on the second, third, and fourth carbons, each with a horizontal bond. - An amino group (NH₂) attached via a vertical bond on the second carbon. - A chlorine atom (Cl) attached to the fifth carbon. - An aldehyde group (CHO) on the terminal carbon. #### c) The third molecule consists of a three-carbon chain with the following: - An OH group on the second carbon with a horizontal bond. - Two bromine atoms (Br) on the first and third carbons. ### Diagrams Each diagram is displayed in a two-dimensional representation, showing different stereochemical orientations through wedges and dashed lines to indicate the spatial arrangement of groups around the chiral centers. This exercise is focused on determining the absolute configuration (R or S) for the chiral centers in each molecule, applying the Cahn-Ingold-Prelog priority rules.
### Assign the Absolute Configuration (R or S) of the Chiral Carbons in the Molecules Below: #### a) The first molecule is a five-membered ring with the following substituents: - A hydroxyl group (OH) attached to the first carbon. - A bromine atom (Br) on the second carbon, with a wedge indicating it projects forward. - A propyl group (CH₂CH₂CH₃) also attached to the second carbon, with a dashed line indicating it projects backward. - A carbonyl group (C=O) on the third carbon. #### b) The second molecule is a carbon chain with multiple functional groups: - A hydroxyl group (OH) on the second, third, and fourth carbons, each with a horizontal bond. - An amino group (NH₂) attached via a vertical bond on the second carbon. - A chlorine atom (Cl) attached to the fifth carbon. - An aldehyde group (CHO) on the terminal carbon. #### c) The third molecule consists of a three-carbon chain with the following: - An OH group on the second carbon with a horizontal bond. - Two bromine atoms (Br) on the first and third carbons. ### Diagrams Each diagram is displayed in a two-dimensional representation, showing different stereochemical orientations through wedges and dashed lines to indicate the spatial arrangement of groups around the chiral centers. This exercise is focused on determining the absolute configuration (R or S) for the chiral centers in each molecule, applying the Cahn-Ingold-Prelog priority rules.
Chemistry
10th Edition
ISBN:9781305957404
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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Given are organic compounds.
R and S configuration is determined by Cahn-Ingold-Prelog rules.
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