Here we go
again on Chemical Bonding (8) but this time its Hydrogen Bonding.
This type of
chemical bonding is just as ubiquitous as van der Waals forces or permanent
dipole bonding in the world of molecules.
But hydrogen
bonding is much stronger than the other two intermolecular bonds.
H bonding
can be as strong as 40-50 kJ per mole.
Evidence
Let’s look
at some of the evidence for this type of bonding starting with a look at the
boiling points of the hydrides of Groups 4, 5, 6 and 7 in the Periodic Table.
The dotted
lines show the expected trend whereas the bold lines indicate the actual
values.
(Incidentally,
there are no continuous variables here, these bold lines are just for purposes
of clarity since Period is a categoric variable not a continuous variable like
boiling point)
What can we
see from this slide?
The boiling
points of water (H2O) ammonia (NH3) and hydrogen fluoride
(HF) seem to be out of synch with the rest of the groups’ hydrides unlike
methane (CH4) which fits the group trends.
Here is more
evidence from how the density of water changes with temperature.
The first surprise looking at this plot is that the density of water at temperatures
just above its melting point is not constant.
This change
in density suggests that water’s
structure as a liquid is changing and in fact liquid water has a structure, the molecules are not just randomly arranged or jumbled together.
And for all
of us telling you that the density of water is 1kg/m3 or 1 g/cm3,
it isn’t at all just look at the variation in those density figures.
Second is
the fact that there is a maximum density at 4oC.
What’s all
this telling us about water?
The obvious thing is that at the bottom of your garden pond in winter when the air temperature is -1oC the water at the bottom of the pond is warmer at 4oC and your fish are not frozen but still alive!!
And then we
can look at evidence from DNA replication how is it that the two strands of the
DNA double helix can unzip and zip up so easily?
How come
carboxylic acids are often found to have double their actual molar mass?
Or how do
the secondary protein structures of the alpha helix and beta pleated sheet
form?
Or
4–nitrophenol has a different molar mass and melting and boiling points to its
analogy isomer 2–nitrophenol?
Let me
explain:
Boiling points of ammonia, water and
hydrogen fluoride
Take the
seemingly anomalous boiling points of ammonia , water and hydrogen fluoride.
These
boiling points cannot just be due to the permanent dipole forces between these
polar molecules nor just the result of the temporary dipoles set up as the
electrons shift from place to place in the molecule.
Both the
permanent dipoles forces and the temporary dipole or London forces are too weak to account for the sudden hike
in boiling point.
Another
force must be involved.
And this force has to be stronger than either
London forces or permanent dipole forces for the hike in boiling point to
be so great.
This
intermolecular force we call a hydrogen bond first recognised by– yes you
guessed it: Linus Pauling—in that famous book of his “The Chemical Bond”.
Here is what
Pauling said of the hydrogen bond in the late 1930’s:
“It was
recognised some decade ago that under certain conditions an atom of hydrogen is
attracted by rather strong forces to two atoms instead of only one so that it
may be considered to be acting as a bond between them. This is called the hydrogen bond.”
Initially it
was thought that these atoms attracted to the hydrogen atom were the highly
electronegative atoms of fluorine, nitrogen or oxygen.
Therefore,
in ammonia a hydrogen bond could form between two ammonia molecules and the
strength of this bond account for ammonia’s higher boiling point.
You can see
that in the diagram the hydrogen bond between the two molecules consists of the
hydrogen from one molecule attracted to the nitrogen of the other incorporating
the lone pair.
So the bond
has a degree of covalency.
The bond
angle of this hydrogen bond contrary to what you may have been taught is not
180o but 160o.
In water the
hydrogen bond angle is 180o
The diagram
below shows the bonding in ice.
Water
molecules in ice are hydrogen bonded twice (look for two dotted lines in the diagram )which leads to an open structure and
therefore a lower density than that of liquid water.
As ice melts
its hydrogen bonded structure collapses and molecules randomly pack closer
together.
The result
is that water reaches its maximum density at 4oC
And hydrogen
fluoride has this structure:
DNA
DNA has two
strands that are bonded together via the base pairs.
These base
pairs bond using hydrogen bonds as in this diagram:
Cytosine and
guanine fit together through the formation of hydrogen bonds as do adenine and
thyamine.
Carboxylic acids
The two
molecules dimerise by forming hydrogen bonds between the carboxyl groups as in
the diagram.
The α-helix and the β-pleated sheet
These two protein secondary structures are supported by the formation of
hydrogen bonds between the amino acid residue side chains as in these two
diagrams:
The dotted lines in the diagrams are the positions of the hydrogen bonds.
Nitrophenol
Here we see in 2-nitrophenol the intramolecular hydrogen bond creating a
hexagonal ring structure.
Name
|
Structure
|
Melting point oC
|
Boiling point oC
|
2-nitrophenol
|
44
|
215
|
|
4-nitrophenol
|
112
|
279
|
The effect of this internal hydrogen bonding is to reduce the melting and
boiling points of the 2- isomer relative to the 4- isomer because there is no
intermolecular hydrogen bonding in the 2- isomer.
You can see in 2-nitrophenol that the H bond is not linear but 120o
In the protein structures, the H—bond is between the N—H group of one
peptide and the C=O group of another i.e. N—H•••O=C where the three dots
represent the H—bond.
So the two electronegative atoms do not have to be the same for an H—bond
to form.
In this
reference here you can read of some of the latest thinking on H—bonds.
This
is the reference to Linus Pauling’s “The Chemical Bond” extract.
Here
is a recent discussion about the definition of the hydrogen bond from the
scientific periodical Nature.
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