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Let us quickly look at the example of a carbon atom. This atom forms 4 single bonds
wherein the valence-shell s orbital mixes with 3 valence-shell p orbitals. This combination
leads to the formation of 4 equivalent sp3 mixtures. These will have a
tetrahedral arrangement around the carbon which is bonded to 4 different atoms.
⇒ Also Read
Chemical Bonding
Molecular Orbital Theory
H2C = CH – CN
HC ≡ C − C ≡ CH
H2C = C = C = CH2
Types of Hybridization
Based on the types of orbitals involved in mixing, the hybridization can be classified as
sp3, sp2, sp, sp3d, sp3d2, sp3d3. Let us now discuss the various types of hybridization, along
with their examples.
sp Hybridization
sp hybridization is observed when one s and one p orbital in the same main shell of an
atom mix to form two new equivalent orbitals. The new orbitals formed are called sp
hybridized orbitals. It forms linear molecules with an angle of 180°
This type of hybridization involves the mixing of one ‘s’ orbital and one ‘p’ orbital
of equal energy to give a new hybrid orbital known as an sp hybridized orbital.
sp hybridization is also called diagonal hybridization.
Each sp hybridized orbital has an equal amount of s and p character – 50% s
and 50% p character.
Examples of sp Hybridization:
sp2 Hybridization
sp2 hybridization is observed when one s and two p orbitals of the same shell of an atom
mix to form 3 equivalent orbitals. The new orbitals formed are called sp2 hybrid orbitals.
sp3 Hybridization
When one ‘s’ orbital and 3 ‘p’ orbitals belonging to the same shell of an atom mix
together to form four new equivalent orbital, the type of hybridization is called
a tetrahedral hybridization or sp3. The new orbitals formed are called sp3 hybrid orbitals.
sp3d Hybridization
sp3d hybridization involves the mixing of 1s orbital, 3p orbitals and 1d orbital to form 5
sp3d hybridized orbitals of equal energy. They have trigonal bipyramidal geometry.
⇒ Also Read:
Hydrogen Bonding
Covalent Bond
Due to the spherical shape of the s orbital, it is attracted evenly by the nucleus from all
directions. Therefore, a hybrid orbital with more s-character will be closer to the nucleus
and thus more electronegative. Hence, the sp hybridized carbon is more electronegative
than sp2 and sp3.
Why is the hybrid orbital during hybridization better than their parent
atoms?
The reason why a hybrid orbital is better than their parents:
1s and 1 p: sp orbitals
1s and 2p: sp2 orbitals
1s and 3p: sp3 orbitals
1s, 3p, and 1d: sp3d orbitals
1s, 3p, and 2d: sp3d2 orbitals
Linear: Two electron groups are involved resulting in sp hybridization, the angle
between the orbitals is 180°.
Trigonal planar: Three electron groups are involved resulting in sp 2 hybridization,
the angle between the orbitals is 120°.
Tetrahedral: Four electron groups involved resulting in sp 3 hybridization, the angle
between the orbitals is 109.5°.
Trigonal bipyramidal: Five electron groups involved resulting in sp 3d hybridization,
the angle between the orbitals is 90°, 120°.
Octahedral: Six electron groups involved resulting in sp 3d2 hybridization, the angle
between the orbitals is 90°.
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as π−bondπ−bond, if all the bonds in the compound are single then there are
only sigma bonds, and pi bonds are present in the double and the triple bonds.
Complete answer: If the compounds are covalent, it means that there are
covalent bonds in them, and there are two types of a covalent bonds, i.e., sigma
By counting the number of bonds, we can calculate the number of sigma and pi
bonds. Sigma and pi bonds are based on the type of bond present in the
molecule, i.e., a single bond, double bond, and triple bond. Therefore, in single
bonds, only a sigma bond is present, in the double bond one is sigma and one is
pi, and in the triple bond one is a sigma bond and two are pi bonds.
HCCH molecule is known as ethyne or acetylene and it is the first member of the
alkyne group, and alkynes are the compounds in which there is a triple bond.
present. Rest there are 3 bonds present, so there are 3 sigma bonds.
Note: The sigma bond is a stronger bond than the pi bond because overlapping
in the sigma bond is along the internuclear axis but in the pi bond there is