CH2 H 29. The compound is correctly called -1,2-dimethylcyclopropane. CH3 CH3 a. cis O b. trans Oc. neither cis nor trans Od. cis and trans isomers are not possible I--5
CH2 H 29. The compound is correctly called -1,2-dimethylcyclopropane. CH3 CH3 a. cis O b. trans Oc. neither cis nor trans Od. cis and trans isomers are not possible I--5
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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
**is correctly called** _______ -1,2-dimethylcyclopropane.
**Options:**
- a. *cis*
- b. *trans*
- c. neither *cis* nor *trans*
- d. *cis* and *trans* isomers are not possible
**Structural Diagram Explanation:**
The chemical structure shown is a cyclopropane ring with two methyl groups (CH₃) attached to adjacent carbon atoms. The spatial positioning of the methyl groups determines whether the compound can have *cis* or *trans* configurations. In this case, examine the orientation of the CH₃ groups in relation to the plane of the cyclopropane ring to determine the correct configuration.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Feeb0e32b-037f-45be-8994-21b63655812d%2F656b7cc8-77a2-4c27-bd28-8e8563164ced%2Ft0ukkkd_processed.png&w=3840&q=75)
Transcribed Image Text:### Question 29:
**The compound**

**is correctly called** _______ -1,2-dimethylcyclopropane.
**Options:**
- a. *cis*
- b. *trans*
- c. neither *cis* nor *trans*
- d. *cis* and *trans* isomers are not possible
**Structural Diagram Explanation:**
The chemical structure shown is a cyclopropane ring with two methyl groups (CH₃) attached to adjacent carbon atoms. The spatial positioning of the methyl groups determines whether the compound can have *cis* or *trans* configurations. In this case, examine the orientation of the CH₃ groups in relation to the plane of the cyclopropane ring to determine the correct configuration.
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