Title: Molecular Shape
1 Chapter 8
2Section 8-1 The Shape of Small Molecules
- If you look at the Lewis structure for a
molecule, you dont usually get an idea of what
the molecule really looks like. - H-N-H
- H
- An ammonia molecule isnt really T-shaped.
3- Chemists use a structural formula to show us what
molecules really look like in 3-D the
ball-and-stick model.
4- molecules look as symmetrical as possible. This
is because of their electrons. - Covalent bonds are just shared pairs of
electrons, and every electron has a negative
charge. So shared pairs will repel other shared
pairs of electrons. - This is actually called the Valence-Shell
Electron Pair Repulsion theory, or VSEPR theory.
5- The VSEPR theory states that in a small molecule,
the pairs of valence electrons are arranged as
far apart from each other as possible.
6- GET OUT YOUR MOLECULAR SHAPE DATA TABLE. THE
INFORMATION THAT WILL HELP YOU FILL IT OUT IS
FOUND ON THE NEXT FEW SLIDES.
7LINEAR
- In a linear molecule, the atoms can be connected
in a straight line. - bond angle 180
- center atom connected to 2 other atoms
- center atom has no unshared electrons
Even the electron pairs that make up double bonds
will repel each other.
8TRIGONAL PLANAR
- Molecules that are trigonal planar have a flat,
triangular shape. - bond angle 120
- center atom connected to 3 other atoms
- center atom has no unshared electrons
9TETRAHEDRAL
- bond angle 109.5
- center atom connected to 4 other atoms
- center atom has no unshared electrons
10PYRAMIDAL
- Pyramidal molecules are shaped like a pyramid,
hence the name. - bond angle 107
- center atom connected to 3 other atoms
- center atom has unshared electrons
Unshared electron pair
11BENT
- bond angle 105
- center atom is connected to 2 other atoms
- center atom has unshared electrons
2 unshared electron pairs
12- Notice that for the tetrahedral shape, the
pyramidal shape, and the bent shape, the atom in
the center is surrounded by 4 pairs of electrons.
So why are the bond angles different???
13- ANSWER Unshared electron pairs exert a greater
repulsive force than shared pairs. - TRANSLATION Unshared pairs take up more room
than shared pairs. - So the bond angle in a pyramidal molecule is a
little smaller than a tetrahedral molecule, and
the bond angle in a bent molecule is a little
smaller than a pyramidal molecule.
14Hybrid Orbitals
- We learned in Chapter 4 that electrons live in
different orbitals in an atom, like the only
orbital in the 2s sublevel, or the 3 orbitals in
the 2p sublevel. This only applies to unbonded
electrons. - When atoms are getting ready to share electrons,
they combine all of their valence electron
orbitals and create new hybrid orbitals.
15- If an atom has 2 electrons it wants to donate to
covalent bonding, it combines 1 s orbital and 1 p
orbital to create 2 sp hybrid orbitals. If an
atom has 3 electrons it wants to donate to
covalent bonding, it combines 1 s orbital and 2 p
orbitals to create three sp2 hybrid orbitals.
p
p
sp2
sp2
sp2
s
16- Linear molecules have sp hybrid orbitals.
Trigonal planar molecules have sp2 hybrid
orbitals. Tetrahedral molecules, pyramidal
molecules, and bent molecules have sp3 hybrid
orbitals.
17Bond Length
- bond length the length of the bond between two
atoms that are sharing electrons - There are two important trends in bond length
- As you go down a group in the periodic table, the
bonds get longer. - Multiple bonds are shorter than single bonds.
18Section 8-2 Polarity
- Remember in a polar bond, electrons are not
being shared equally. That makes one end of the
bond slightly negative and the other end slightly
positive. - A polar molecule (a.k.a. dipole) is a molecule
that has two oppositely charged ends. Polar
molecules act like little magnets.
19- If a molecule contains only nonpolar covalent
bonds, it is automatically a nonpolar molecule. - If a molecule contains some polar bonds or all
polar bonds, it may or may not be polar. The
polarity of a molecule is determined by the
polarity of its bonds AND by the shape of the
molecule.
20Example 1 Formaldehyde
The difference in electronegativity between
Oxygen and Carbon is 1.0, so the bond is clearly
polar.
O
The three green arrows show the direction of the
shift in negative charge based on the polarity of
each bond. All three arrows point up toward the
top of the molecule, so overall, the molecule is
polar. The oxygen end is negative, and the
hydrogen end is positive.
C
H
H
The difference in electronegativity between
Carbon and Hydrogen is 0.4, so these two bonds
are just barely polar.
21Example 2 Carbon Dioxide
C
O
O
The difference in electronegativity between
Oxygen and Carbon is 1.0, so both bonds are polar.
The two green arrows show the direction of the
shift in negative charge based on the polarity of
each bond. The arrows point in opposite
directions, so there is no way the molecule can
be polar.
22Example 3 Water
O
The two green arrows show the direction of the
shift in negative charge based on the polarity of
each bond. Both arrows point toward the oxygen,
so the oxygen end of the molecule is negative,
and the hydrogen end is positive. This molecule
is polar.
H
H
The difference in electronegativity between
Oxygen and Hydrogen is 1.4, so both bonds are
polar.
23BIG SHORTCUT!!!
- Linear, trigonal planar, and tetrahedral
molecules will be nonpolar AS LONG AS the atoms
around the center are all the same element. - Bent and pyramidal molecules are always polar.
24Large Molecules
- For small molecules, the shape helps determine
the polarity. The opposite is true for large
molecules the polarity helps determine the
shape.
25- One example of a large molecule is a protein.
Proteins are long chains of subunits. Some
subunits have side-chains that are polar, and
other subunits have side-chains that are
nonpolar. The polar side-chains on different
subunits act like magnets to attract each other
and stick together. This makes the whole chain
kink and bend, kind of like the cord on your
telephone.
26 subunit
polar side-chain
nonpolar side-chain
Because the polar side-chains are attracted to
each other, the whole protein strand will kink up.