H H Determine the relationship between the two compounds shown here. A) stereoisomers B) geometric isomers H C) constitutional isomers D) optical isomers E) They are not related. H
H H Determine the relationship between the two compounds shown here. A) stereoisomers B) geometric isomers H C) constitutional isomers D) optical isomers E) They are not related. H
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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![**Chemistry Educational Content: Understanding Isomers**
**Question 23 of 30**
**Determine the relationship between the two compounds shown here.**
The image shows structural representations of two chemical compounds. The compounds have different spatial arrangements of atoms around a double bond, which can be identified by examining the positions of the hydrogen atoms (H):
- The left compound contains a double bond with hydrogen atoms on opposite sides.
- The right compound contains a double bond with hydrogen atoms on the same side.
**Answer Choices:**
A) Stereoisomers
B) Geometric isomers
C) Constitutional isomers
D) Optical isomers
E) They are not related.
**Analysis:**
- **Stereoisomers**: This category includes compounds that have the same structural formula but differ in the spatial arrangement of atoms.
- **Geometric isomers (cis/trans)**: A subtype of stereoisomers where compounds differ in the spatial arrangements around a double bond or ring structure.
- **Constitutional isomers**: Compounds that have the same molecular formula but different connectivity of their atoms.
- **Optical isomers (enantiomers)**: A subtype of stereoisomers where compounds differ in the arrangement of atoms such that they are non-superimposable mirror images.
- **They are not related**: Indicates no specific relationship between the compounds.
**Conclusion:**
The given compounds are **Geometric isomers (B)**, specifically *cis-trans* isomers, due to the difference in the spatial arrangement of the hydrogen atoms around the double bond.
This type of isomerism occurs when each carbon of a carbon-carbon double bond has two different substituents, leading to different physical properties and reactivity.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F55a44e3d-6d6a-4ecd-9343-ab7bc7f808c7%2F1bbe1c82-6139-4ee9-8c6d-7938cce6644c%2Ftyr3mir_processed.jpeg&w=3840&q=75)
Transcribed Image Text:**Chemistry Educational Content: Understanding Isomers**
**Question 23 of 30**
**Determine the relationship between the two compounds shown here.**
The image shows structural representations of two chemical compounds. The compounds have different spatial arrangements of atoms around a double bond, which can be identified by examining the positions of the hydrogen atoms (H):
- The left compound contains a double bond with hydrogen atoms on opposite sides.
- The right compound contains a double bond with hydrogen atoms on the same side.
**Answer Choices:**
A) Stereoisomers
B) Geometric isomers
C) Constitutional isomers
D) Optical isomers
E) They are not related.
**Analysis:**
- **Stereoisomers**: This category includes compounds that have the same structural formula but differ in the spatial arrangement of atoms.
- **Geometric isomers (cis/trans)**: A subtype of stereoisomers where compounds differ in the spatial arrangements around a double bond or ring structure.
- **Constitutional isomers**: Compounds that have the same molecular formula but different connectivity of their atoms.
- **Optical isomers (enantiomers)**: A subtype of stereoisomers where compounds differ in the arrangement of atoms such that they are non-superimposable mirror images.
- **They are not related**: Indicates no specific relationship between the compounds.
**Conclusion:**
The given compounds are **Geometric isomers (B)**, specifically *cis-trans* isomers, due to the difference in the spatial arrangement of the hydrogen atoms around the double bond.
This type of isomerism occurs when each carbon of a carbon-carbon double bond has two different substituents, leading to different physical properties and reactivity.
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