Sei sulla pagina 1di 3

James Yu Chem I

Chapter 9: Concepts and Definitions


Hybridization – The mixing of native atomic orbitals to form special

orbitals for bonding

Sigma Bond – In each of these bonds, the electron pair is shared in an

area centered on a line running between the atoms

Pi Bond – Parallel p orbitals share an electron pair, which occupies the

space above and below a line joining the atoms

Bonding Molecular orbital – lower in energy than the atomic orbitals of

which it is composed

Antibonding Molecular Orbital – higher in energy than the atomic

orbitals of which it is composed

Bond Order – the difference between the number of bonding electrons

and the number of antibonding electrons divided by two

Homonuclear diatomic molecules – composed of two identical atoms

Heteronuclear diatomic molecules – different atoms

Paramagnetism – causes the substance to be attracted into the inducing

magnetic field

Diamagnetism – causes the substance to be repelled from the inducing

magnetic field

Delocalized – the condition where the electrons in a molecule are not

localized between a pair of atoms but can move throughout the molecule

Hybridization and the Localized Electron Model

Let us consider methane:

1) Using the 2p and 2s atomic orbitals will lead to two different types of
C—H bonds: Those from the overlap of a 2p orbital of carbon and a 1s
orbital of hydrogen and those from the overlap of a 2s orbital of
carbon and a 1s orbital of hydrogen. This is a problem because
methane is known to have four identical C—H bonds.
2) Since the carbon 2p orbitals are mutually perpendicular, we might
expect the three C—H bonds formed with these orbitals to be oriented
at 90-degree angles. However, the methane molecule is known by
experiment to be tetrahedral with bond angles of 109.5 degrees.

What really happens then? The 2s and 2p orbitals in carbon hybridize to

form sp3 orbitals. They are somewhat mushroomed shaped and make a
tetrahedral arrangement.

Whenever a set of equivalent tetrahedral atomic orbitals is required by an

atom, this model assumes that the atom adopts a set of sp3 orbitals; the
atom becomes sp3 hybridized.

Sp2 Hybridization

In ethylene, the sp3 orbitals we just considered will not work because
they are at angles of 109.5 degrees rather than the required 120 degrees.
These angles can be obtained by combining one s orbital and two p
orbitals, this is called sp2 hybridization.

The three sp2 orbitals on each carbon can be used to share electrons.
This type of bonding is called a sigma bond. But how can we explain the
double bond? The second bond is the result from sharing an electron
pair above and below the sigma bond, this type of bond is called a pi

The Localized Electron Model

• Draw the Lewis structures

• Determine the arrangement of electron pairs using the VSEPR model.
• Specify the hybrid orbitals needed to accommodate the electron pairs.
The Molecular Orbital Model

1. The electron probability of both molecular orbitals is centered along

the line passing through the two nuclei.
2. In the molecule only the molecular orbitals are available for
occupation by electrons.
3. The electrons will fill the MO1 before filling in the MO2, that is because
it is lower in energy than the latter. There are now two classes of
electrons, bonding and antibonding.

Bond Order

To indicate bond strength, we use the concept of bond order. Bond order
is the difference between the number of bonding electrons and the
number of antibonding electrons divided by two. The higher the bond
order, the more stable the atom is.