Consider the molecule acetonitrile (CH3CN)
1. Which of the following must be overcome during the boiling of acetonitrile?
1. dispersion forces
2. dipole-dipole forces
3. hydrogen bonds
Which of the following must be overcome during the boiling of acetonitrile?
1. dispersion forces
2. dipole-dipole forces
3. hydrogen bonds
2 only
1 and 3
1 and 2
1 only
1, 2, and 3
2.
Shown above are the shorthand structures of phenylacetic acid and 1-octadecylamine. Recall that lines represent two-electron bonds. Ends of lines and junctures represent carbon atoms. Finally, hydrogen atoms bonded to carbon are omitted for clarity.
The solubility of phenylacetic acid in acetonitrile is 3.87 M and the solubility of 1-octadecylamine in acetonitrile is 0.08 M
Select the response that BEST rationalizes the relative solubilities
a. The dispersion forces in 1-octadecylamine are very favorable
b. Phenylacetic acid can form hydrogen bonds with the nitrogen in acetonitrile while 1-octadecylamine cannot form hydrogen bonds with the nitrogen in acetonitrile
c. There are no favorable dipole-dipole interactions between acetonitrile and 1-octadecylamine
d. The molecular weight of phenylacetic acid is closer to the molecular weight of acetonitrile
Consider the molecule acetonitrile (CH3CN)
1. Which of the following must be overcome during the boiling of acetonitrile?
1. dispersion forces
2. dipole-dipole forces
3. hydrogen bonds
Which of the following must be overcome during the boiling of acetonitrile?
1. dispersion forces
2. dipole-dipole forces
3. hydrogen bonds
2 only | |
1 and 3 | |
1 and 2 | |
1 only | |
1, 2, and 3 |
2.
Shown above are the shorthand structures of phenylacetic acid and 1-octadecylamine. Recall that lines represent two-electron bonds. Ends of lines and junctures represent carbon atoms. Finally, hydrogen atoms bonded to carbon are omitted for clarity.
The solubility of phenylacetic acid in acetonitrile is 3.87 M and the solubility of 1-octadecylamine in acetonitrile is 0.08 M
Select the response that BEST rationalizes the relative solubilities
a. The dispersion forces in 1-octadecylamine are very favorable
b. Phenylacetic acid can form hydrogen bonds with the nitrogen in acetonitrile while 1-octadecylamine cannot form hydrogen bonds with the nitrogen in acetonitrile
c. There are no favorable dipole-dipole interactions between acetonitrile and 1-octadecylamine
d. The molecular weight of phenylacetic acid is closer to the molecular weight of acetonitrile