Types of Intermolecular Forces: At the end of this section, students should be able to:
Describe the types of intermolecular forces present in condensed phases, including dispersion forces, dipole-dipole attractions, and hydrogen bonding.
Identify the intermolecular forces experienced by specific molecules based on their structures.
Explain the relationship between intermolecular forces and the temperatures related to physical state changes.
The kinetic molecular theory helps explain the behavior of solids and liquids.
Particles in solids:
Tightly packed and arranged in regular patterns.
Vibrate in fixed positions but do not move relative to one another.
Particles in liquids:
Close together but lack a fixed arrangement.
Move past each other, remaining in constant contact.
Particles in gases:
Spread far apart with no regular arrangement.
Move independently except during collisions.
The phase of a substance depends on:
The strength of the attractive intermolecular forces (IMFs).
The kinetic energy (KE) of the molecules.
Intermolecular forces (IMFs): forces of attraction between particles (atoms, molecules, or ions).
These forces keep particles close together, while kinetic energy provides the energy that allows particles to overcome these forces during temperature changes.
Changes in physical state occur when temperature or pressure conditions favor shifts in intermolecular forces.
When water vapor cools sufficiently, the attractions between water molecules allow condensation from gas to liquid.
Example applications:
Cold glass causing moisture to condense from air, forming liquid water on its surface.
Many gases can liquefy under high pressure, compressing molecules closer together to allow intermolecular attractions to dominate over their kinetic energy.
For instance, Butane (C₄H₁₀) is gas at standard conditions but condenses into liquid in a lighter's fuel compartment.
Attractive forces between molecules (intermolecular forces) differ from those within molecules (intramolecular forces).
Intramolecular forces: bonds within molecules (e.g., covalent bonds); much stronger than IMFs.
To break IMFs, relatively low energy is needed, while breaking covalent bonds requires significantly more energy.
Example: To convert 1 mole of liquid HCl to gas, only about 17 kJ is needed compared to approximately 430 kJ to break H-Cl bonds.
London dispersion forces are present in all condensed phases.
Temporary dipoles form when electron distributions in atoms or molecules change, leading to weak attractions.
Larger, heavier atoms have stronger dispersion forces than smaller, lighter ones due to more substantial electron cloud distortions.
Polar molecules have a distinct positive and negative end, creating a dipole.
Dipole-dipole attractions occur between the positive end of one molecule and the negative end of another, as seen in molecules such as HCl.
Particularly strong dipole-dipole interactions occur when hydrogen is bonded to highly electronegative atoms such as F, O, or N.
This results in significant attractions evident in substances like water (H₂O), leading to higher boiling points compared to nonpolar counterparts.
As the molecular size increases, boiling and melting points generally increase due to stronger dispersion forces.
The shape of molecules affects dispersion strength—elongated shapes have more surface area for intermolecular contact than compact shapes, enhancing attraction and boiling points.
Example: n-pentane has a higher boiling point due to its larger contact area compared to neopentane.
Geckos can adhere to surfaces due to intermolecular forces acting through their feet, which are covered with tiny hairs (setae).
These setae maximize surface area contact, enabling the gecko to stick to various surfaces without adhesive substances.
Their ability to toggle adhesion is due to the change in angles between the spatulae on their toes when under force, illustrating the practical application of dispersion forces.