Solutions to IMF Exercises

Answers/Solutions to Exercises

Exercises

Exercise 1. Indicate the intermolecular forces experienced by each of the following molecules.

a) PCl3
This is a polar molecule.

Lewis structure of PCl<sub>3</sub >

It experiences both London dispersion forces and dipole-dipole forces of attraction.

b) PCl5

This is a non polar molecule.

Lewis structure of PCl5.

It only experiences London dispersion forces.

c) C4H10

This is a nonpolar molecule.

Lewis structure of butane

It only experiences London dispersion forces.

d) CH2F2

This molecule is polar.

Lewis structure of CH<sub>2</sub>F<sub>2</sub>

It experiences both London dispersion forces and dipole-dipole forces of attraction.

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Exercise 2. Indicate the intermolecular forces that are experienced by each of the following.

a) CH3OH

This molecule is polar.

Lewis structure of methanol

It experiences both London dispersion and dipole-dipole forces of attraction. In addition, hydrogen is bonded to oxygen, and it experiences hydrogen bonding.

b) O2

O2 is nonpolar. It only experiences London dispersion forces

Lewis structure of O<sub>2</sub>

c) CHCl3

This molecule is polar. It experiences London dispersion and dipole-dipole forces of attraction.

Lewis structure of CHCl<sub>3</sub>
d) H2Se

This molecule is polar. It has a bent shape. It experiences both London dispersion and dipole-dipole attractive forces.

Lewis structure of SeH<sub>2</sub>

e) C10H22

This molecule is nonpolar. It only experiences London dispersion forces.

Lewis Structure of decane

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Exercise 3. Below are the boiling points of some substances.

methane, CH4, (-164°C)
methanol, CH3OH, (64.7°C)

decane, C10H22, (174°C)
1-decanol, C10H21OH, (231°C)

Lewis structures of methane and methanol

Explain why methanol has a boiling point that is 229 degrees higher than that of methane while 1-decanol boils only 57 degrees higher than decane.

Both methane and methanol have small dispersion forces of attraction. Methanol can hydrogen bond which explains the much higher boiling point.

Both 1-decanol and decane have large similar dispersion forces. The 1-decanol can also hydrogen bond, which is why it has a 57 degree higher boiling point than decane. The London dispersion forces are much stronger in decane and decanol than in methane and methanol.

Lewis structures of decane and decanol

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Exercise 4. Draw a sketch of the hydrogen bonding in several molecules of methanol, CH3OH.

Hydrogen bonding in methanol molecules

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Exercise 5. Which substance in each pair has the highest boiling point?

a) S2F2 or S2Cl2

Lewis structures of S<sub>2</sub>F<sub>2</sub> and S<sub>2</sub>Cl<sub>2</sub>

S2Cl2 has the highest boiling point. Both molecules have a bent molecular geometry about the sulfur atoms, but Cl is larger than F, therefore, the dispersion forces are greater in S2Cl2 than in S2F2.

b) NH3 or PH3

Lewis structures of NH<sub>3</sub> and PH<sub>3</sub>

Both molecules are polar, but NH3 also has intermolecular hydrogen bonding. NH3 has the highest boiling point.

c) H2S or H2Te

H2Te has the higher boiling point. Both molecules are polar, have a bent molecular geometry, and experience dipole-dipole forces. They both experience London dispersion forces. H2Te has the higher boiling point because Te is heavier than S and therefore H2Te experiences stronger dispersion forces.

d) NOF or NOCl

Lewis structures for NOF and NOCl

Both molecules have London dispersion forces and dipole-dipole attractive forces. Their molecular geometry is trigonal pyramidal. The NOCl has a higher boiling point because Cl is heavier than F, and therefore the dispersion forces of attraction are stronger in NOCl.

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Exercise 6. Identify the intermolecular forces for each of the following substances.

a) HO(CH2)2OH, ethylene glycol

This molecule experiences London dispersion, dipole-dipole, and hydrogen bonding forces of attraction. The hydrogen bonding forces are especially strong since there are two hydroxyl groups.

Lewis structure of ethylene glycol

b) NH2OH, hydroxylamine

Lewis Structure NH2OH

This molecule experiences London dispersion, dipole-dipole, and hydrogen bonding forces of attraction.

c) PH3O, phosphine oxide

Lewis structure of PH<sub>3</sub>O

The molecule is polar and experiences both London dispersion forces and dipole-dipole forces.

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