Intermolecular Forces
Intermolecular Forces
The basic assumptions of the kinetic molecular theory (KMT) common to the three states of
matter are: they are composed of molecules though not all times for solids and these possess kinetic
energy.
The other assumptions are meant mainly to account for the properties of gases, particularly
those referring to the motion, the amount of kinematic energy, the distance, and the attraction
between the molecules or particles. However, comparison in terms of these assumptions shows the
similarities and differences of matter existing as gases, liquids, and solids.
Thus, the shape and volume of matter in the three states are explained as follows:
1. The shape and volume of gases are not definite because the molecules are widely separated,
have negligible attraction for one another, and are constantly moving rapidly in all
directions so they can fill any shape and size of container.
2. Liquid molecules are close enough to touch one another. They have attractive forces to
keep them together so that the total volume of a certain amount of them is definite. Since
they can still move, slipping and sliding over one another, the liquid continues to conform
to the shape of its container.
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3. Solid particles are closely packed because of strong attractive forces among them. Their
low kinetic energies cause them to stay in fixed positions, resulting in definite shape and
volume. At the atomic level, however, vibrational motion of the molecules is observed.
Section Assessment
1. How do liquids and solids compare with gases in terms of attractive forces?
2. How are attractive forces related to the motion and the amount of kinetic energy of the
particles?
Intermolecular Forces
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the electrical fields of the adjacent molecules. Thus, the induced polarization of molecules
produced by the fluctuations of charges cause those close enough and properly oriented molecules
to attract each other.
The Van der Waals type of attraction between nonpolar groups is a nonspecific attractive
force between two molecules that are about 3 to 4 Angstrom apart. It is a weak interaction with a
bond energy of about 1 kcal/mol for a pair of atoms. It is considered weaker than electrostatic and
hydrogen bonds, but nonetheless, important.
Dipole-dipole Forces
Dipole-dipole interaction is the attraction of bond dipoles in different molecules. Bond
dipoles arise from the unequal sharing of electrons by covalently bonded atoms. The tendency of
dipoles to be perfectly oriented with respect to one another is observed to be effective at reasonably
larger distances than Van der Waals forces.
The following are illustrations of the manner by which dipole-dipole forces act.
( The solid lines represent covalent bonds; the dotted lines are dipole-dipole forces.)
For water molecules, the dipole-dipole interaction is represented as:
In which the hydrogens from the + end and the O forms the -end of the water dipole.
Ion -Dipole Forces
These forces exist when polar molecules are attracted to ions. The positive pole is attracted
to a negative ion (anion), while the negative pole is attracted to a positive ion (cation).
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Ion-dipole interactions are involved in solution processes like in the case of sodium
chloride dissolving in water. When, for example, sodium chloride crystal is placed in water, the
polar ends of the water molecules exert attractive forces on the surface ions of the crystal (Oδ- ends
attracts Na+ ions as shown in Figure 1.5. (A); Hδ+ ends attracts Cl- ions as shown in Figure 1.5.(B)
and pull them away from each other, preventing them from rejoining as each ion is surrounded by
water molecules.
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Note: Compounds that have significant
hydrogen bonding ability are those that
contain hydrogen covalently bonded to
F, O, or N.
These intermolecular forces are weaker than either ionic or covalent bonds, but their
importance cannot be underestimated. They are responsible for determining whether a molecular
compound is a gas, a liquid, or a solid at a given temperature. They also account for the differences
in some physical properties of matter in the different phases.
Reference:
Authors:
Luciana V. Ilao
Betty M. Lontoc
Edwehna Ellinore S. Paderna-Gayon
Coordinator:
Josefina Gironella-Belen
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