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
G, J, and K please! I am checking my work and wanted to make sure that I'm naming these correctly, any help would be great!:)
give the name and assign R/S and E/Z configurations when appropriate

Transcribed Image Text:**G)**
- The chemical structure features a cyclohexane ring with several substituents.
- A bromine (Br) atom is connected to the ring.
- A cyclopropyl group is attached, slightly affecting the overall shape of the molecule.
- A carbonyl group (C=O) with an adjacent hydrogen (H) is present.
**J)**
- This structure includes an amide functional group highlighted by an NHCH₃ side chain.
- A carbonyl group (C=O) is also present, forming part of the structure.
- The double bonds are depicted, showing the molecule's unsaturation and geometry.
**K)**
- The chemical diagram includes a hydroxy group (OH) connected to a chiral center.
- The structure consists of an additional chain with ketone groups (C=O).
- Each segment illustrates the molecular complexity, showing stereochemistry with wedges indicating three-dimensional structure.
Expert Solution

Step 1
R and S given by CIP rule in which prority is given that group which is Directly attached to the chiral centre and which have highest atomic mass
If we rotate in clockwise direction and 4th group is not at dash position then Use S configuratuon
And if 4th group is at dash position then use R configuratuon or vice versa
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Solved in 2 steps with 1 images

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