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MADE BY
XYZ
ACKNOWLEDGEMENT
I would like to express my greatest
gratitude to the people who have
helped & supported me throughout
my project. I am grateful to my
teacher
Mrs.Anushka
ORBITAL
HYBRIDIZATION
OF THE probable
SP ORBITAL HYBRIDIZATION
Be
Be
Be
Be
2s + 2pz
and
Be
2s - 2pz
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C
2s
+ C +
2px
2pz
=
sp2
2px
y
z
+
2pz
2py
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Groups
of
Hybridization
Electrons
Ideal
Bond
Angle
sp
180
sp2
120
sp3
109.5
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H Be H
H
H C C N
sp3 C H sp C
sp2 C
C O
O
H O N sp2 N
sp3 O
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BERYLLIUM SP HYBRIDIZATION
Be
Be
Be
and
Be
Two orbitals
each can hold two electrons
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SP HYBRIDIZATION
2p
energy
px, py
sp
2s
ao
atomic
orbtials
hao
Be
Maximum angle that
two orbitals can be
apart is 180.
hybrid atomic
orbtials
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SP HYBRIDIZED BERYLLIUM
VALENCE ORBITALS
The other p-orbitals
of beryllium (px, py)
x
remain unchanged
y
Be
SP HYBRIDIZED BERYLLIUM
VALENCE ORBITALS
The other p-orbitals
Why is it a linear molecule?
of beryllium (px, py)
remain unchanged
H
Be
two sigma
bonds
H
Be
H
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H
H C C N sp N
sp3 C H sp C
sp2 C
C O sp2 O
O
H O N sp2 N
sp3 O
sp3 N
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sp3 O
sp2 C
sp3 N
sp2 N
sp3 C
sp C
sp2 O
sp N
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ETHENE
H
H
C C
H
H
2py
SP2 HYBRIDIZATION
energy
sp2
2s
ao
hao
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ETHENE
Top down view
(xz plane)
Edge on view
ETHENE
H
H
carbon-carbon pi bond
due to 2py- 2py overlap
H
C
carbon-hydrogen
sigma bonds
due to sp2-s overlap
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METHANE
H
H C H
H
sp3
energy
2p
SP3 HYBRIDIZATION
All four hybrid
atomic orbitals
have the same
energy.
2s
carbon
ao
hao
These four orbitals are
energetically degenerate.
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METHANE
H
carbon-hydrogen
sigma bonds
due to sp3-s overlap
H C
H
H
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AMMONIA
H N H
H
The 2s, 2px , 2py and 2pz atomic orbitals of nitrogen
are used
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sp3
energy
2p
SP3 HYBRIDIZATION
2s
nitrogen
ao
hao
By hybridizing its
atomic orbitals
nitrogen gains
more stable
(lower energy)
orbitals for bonding.
AMMONIA
a completely filled in
orbital contains
two electrons
nitrogen-hydrogen
sigma bonds
due to sp3-s overlap
H N
H
H
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HYDROGEN
CYANIDE
H C N
hydrogen
1s orbital
carbon
sp hybridized
nitrogen
sp hybridized
HYDROGEN
CYANIDE
H C N
sigma bonds
px orbital
overlap
py orbital
overlap
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H C N
HYDROGEN CYANIDE
sigma bonds
2 pi bonds
(between carbon
and nitrogen)
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NITRITE ION
N
O
O
3 groups of electrons
around nitrogen
sp2 hybridization
O-N-O @ 120
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N
O
O
NITRITE ION
-1 charge
_ ___ _
1s sp2 p
_ ____
1s
sp3
NITRITE ION
O N O
N
O
O
3 groups of electrons
around nitrogen
sp2 hybridization
O-N-O @ 120
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ETHENE
H H
C C
H H
H
H
C C
H
H
3 groups of electrons
around carbon
sp2 hybridization
C-C-H @ 120
H-C-H @ 120
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ETHANE
H H
H C C H
H H
H H
H C C H
H H
4 groups of electrons
around carbon
sp3 hybridization
C-C-H @ 109.5
H-C-H @ 109.5
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DIPOLE MOMENTS
CHARGE IS NOT ALWAYS EQUALLY
DISTRIBUTED IN A MOLECULE.
03/17/15
PREDICTIONS
FOR MOLECULAR COMPOUNDS
SOLUBILITY AND MISCIBILITY ARE RELATED TO THE POLARITY (I.E.,
DIPOLE MOMENT) OF THE MOLECULE.
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CARBONATE ION
O 2C
O
POLARITY PREDICTIONS
RANK THE FOLLOWING MOLECULES IN TERMS
OF POLARITY:
Cl
C
Cl
Cl
03/17/15