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:**
What are the intermolecular forces of 1,3-diphenyl-2-propyn-1-one?
---
**Answer:**
Intermolecular forces in 1,3-diphenyl-2-propyn-1-one include:
1. **London Dispersion Forces:** Present in all molecules, these are weak interactions due to temporary dipoles in the electron cloud.
2. **Dipole-Dipole Interactions:** Arising from the polar carbonyl group (C=O), where there is a partial negative charge on the oxygen and partial positive on the carbon.
3. **π-π Interactions:** Due to the aromatic phenyl rings, which can engage in stacking interactions with each other.
These forces contribute to the molecule's physical properties, such as boiling and melting points, solubility, and volatility.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fb2247daf-e6e1-4841-93f4-801ac9a165b4%2F17d64729-b11a-4dc3-910d-9f2d54cd220a%2Fy7k4c4_processed.png&w=3840&q=75)
Transcribed Image Text:**Question:**
What are the intermolecular forces of 1,3-diphenyl-2-propyn-1-one?
---
**Answer:**
Intermolecular forces in 1,3-diphenyl-2-propyn-1-one include:
1. **London Dispersion Forces:** Present in all molecules, these are weak interactions due to temporary dipoles in the electron cloud.
2. **Dipole-Dipole Interactions:** Arising from the polar carbonyl group (C=O), where there is a partial negative charge on the oxygen and partial positive on the carbon.
3. **π-π Interactions:** Due to the aromatic phenyl rings, which can engage in stacking interactions with each other.
These forces contribute to the molecule's physical properties, such as boiling and melting points, solubility, and volatility.
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