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Ⓡ 5. Assign the R and S configurations for all stereogenic centers in the following compounds. H BI!!!! Br Br WOH H₂C H CH₂ H -H CH₂ CH(CH₂)₂ (b) CH=CH₂ H+C=C -C=CCH₂ CH₂CH₂CH₂C1 CH₂CH₂Cl H₂NH CH₂CH₂Cl CH₂CH₂CH₂OH H₂N CH₂CH₂OH

Ⓡ 5. Assign the R and S configurations for all stereogenic centers in the following compounds. H BI!!!! Br Br WOH H₂C H CH₂ H -H CH₂ CH(CH₂)₂ (b) CH=CH₂ H+C=C -C=CCH₂ CH₂CH₂CH₂C1 CH₂CH₂Cl H₂NH CH₂CH₂Cl CH₂CH₂CH₂OH H₂N CH₂CH₂OH

Chemistry
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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**Question 5:** Assign the R and S configurations for all stereogenic centers in the following compounds. **Diagrams:** - **(a)** Features a tetrahedral carbon center bonded to a bromine (Br), hydrogen (H), hydroxyl group (OH), and a propyl group (CH(CH₃)₂). This center is a chiral carbon. - **(b)** Shows a carbon center involved in a double bond, attached to another carbon chain (CH=CH₂), a halogen (Cl), and two hydrogens. No chiral center present due to the double bond. - **(c)** Displays a complex organic molecule with two chiral centers, each connected to chlorine (Cl) atoms. - **(d)** Demonstrates a carbon molecule with two identical bromo (Br) groups on opposite sides, along with two hydrogen (H) atoms. It forms a symmetrical structure with no chiral center. - **(e)** Depicts a central carbon bonded to an amino group (NH₂), hydrogen (H), and two identical ethyl chloride groups (CH₂CH₂Cl). The amino group creates a chiral center. - **(f)** Consists of a central carbon attached to an amino group (NH₂), hydrogen (H), a methyl group (CH₃), and an ethylene glycol group (CH₂CH₂OH). The carbon is a chiral center. These diagrams illustrate various molecular configurations, requiring the assignment of R and S configurations based on the spatial arrangement of atoms around each chiral carbon center.
Transcribed Image Text:**Question 5:** Assign the R and S configurations for all stereogenic centers in the following compounds. **Diagrams:** - **(a)** Features a tetrahedral carbon center bonded to a bromine (Br), hydrogen (H), hydroxyl group (OH), and a propyl group (CH(CH₃)₂). This center is a chiral carbon. - **(b)** Shows a carbon center involved in a double bond, attached to another carbon chain (CH=CH₂), a halogen (Cl), and two hydrogens. No chiral center present due to the double bond. - **(c)** Displays a complex organic molecule with two chiral centers, each connected to chlorine (Cl) atoms. - **(d)** Demonstrates a carbon molecule with two identical bromo (Br) groups on opposite sides, along with two hydrogen (H) atoms. It forms a symmetrical structure with no chiral center. - **(e)** Depicts a central carbon bonded to an amino group (NH₂), hydrogen (H), and two identical ethyl chloride groups (CH₂CH₂Cl). The amino group creates a chiral center. - **(f)** Consists of a central carbon attached to an amino group (NH₂), hydrogen (H), a methyl group (CH₃), and an ethylene glycol group (CH₂CH₂OH). The carbon is a chiral center. These diagrams illustrate various molecular configurations, requiring the assignment of R and S configurations based on the spatial arrangement of atoms around each chiral carbon center.
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