For each solute, tap the button under the better solvent. solute Which is the better solvent? H :0: H, С — С — Он :0: H. NH, - C- NH, H CH; (CH,),CH, CH;CH,OH :0: :0: :0: но — с — сн, — сн, — с — он | CH,-S- CH,
For each solute, tap the button under the better solvent. solute Which is the better solvent? H :0: H, С — С — Он :0: H. NH, - C- NH, H CH; (CH,),CH, CH;CH,OH :0: :0: :0: но — с — сн, — сн, — с — он | CH,-S- CH,
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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 |  |
| NH<sub>2</sub>--C==O--NH<sub>2</sub> |  |
| | CH<sub>3</sub>(CH<sub>2</sub>)<sub>3</sub>CH<sub>3</sub> |
|  |  |
| HO--C==O--CH<sub>2</sub>--CH<sub>2</sub>--C==O--OH |  |
| | CH<sub>3</sub>--S==O--CH<sub>3</sub> |
| CaCl<sub>2</sub> |  |
| |  |
| | CH<sub>3</sub>OH |
When deciding which solvent is better, consider the chemical characteristics and similarities between the solute and the solvent. Similar types of bonding, polarity, and functional groups typically lead to better solubility.
#### Explanations of Graphs and Diagrams:
1. **First Solute-Solvent Pair**:
- **Solute**: Urea (NH<sub>2</sub>--C==O--NH<sub>2</sub>), which contains a carbonyl group flanked by two amine groups.
- **Solvents**:
- A molecule containing an aromatic ring with a carboxyl group (likely benzoic acid).
- n-Hexane (CH<sub>3</sub>(CH<sub>2</sub>)<sub>3](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2Fada93b44-8b7d-4f67-9ba6-5f5a01e75f14%2F3ac2d48e-0f4b-47c1-ad57-4cb94930ff64%2F6o9fgb_processed.jpeg&w=3840&q=75)
Transcribed Image Text:### Solubility Exercise
For each solute, tap the button under the better solvent.
| Solute | Which is the Better Solvent? |
|-------------------------------------------------|------------------------------------------------------|
|  |  |
| NH<sub>2</sub>--C==O--NH<sub>2</sub> |  |
| | CH<sub>3</sub>(CH<sub>2</sub>)<sub>3</sub>CH<sub>3</sub> |
|  |  |
| HO--C==O--CH<sub>2</sub>--CH<sub>2</sub>--C==O--OH |  |
| | CH<sub>3</sub>--S==O--CH<sub>3</sub> |
| CaCl<sub>2</sub> |  |
| |  |
| | CH<sub>3</sub>OH |
When deciding which solvent is better, consider the chemical characteristics and similarities between the solute and the solvent. Similar types of bonding, polarity, and functional groups typically lead to better solubility.
#### Explanations of Graphs and Diagrams:
1. **First Solute-Solvent Pair**:
- **Solute**: Urea (NH<sub>2</sub>--C==O--NH<sub>2</sub>), which contains a carbonyl group flanked by two amine groups.
- **Solvents**:
- A molecule containing an aromatic ring with a carboxyl group (likely benzoic acid).
- n-Hexane (CH<sub>3</sub>(CH<sub>2</sub>)<sub>3
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