A handy way to model covalent bonding

Lewis dot structures (or just Lewis structures) were developed around 1920 by pioneering chemist Gilbert Lewis, as a way of picturing chemical bonding in molecules.

We draw Lewis structures to

Discover the bonding arrangement of atoms,

Discover whether there is any degeneracy of bonding (more on that later), and

Figure out whether a given group of atoms might even bond together to form a molecule at all.

In a Lewis structure, every atom is surrounded by dots that represent its valence-shell electrons. So nitrogen (N) would look like this:

nitrogen dot

Sometimes we draw the electrons of different atoms with different colors or symbols so we can keep track of them, like this:

NOH Lewis

OK, let's learn how to use Lewis structures.


Example 1: Methane, CH4

You might have seen the bonding of methane already in the section on covalent bonding. With Lewis structures, we take a trial-and-error approach to figuring out bonding patterns. The goal is to make sure that each atom is surrounded by eight dots (two for hydrogen), representing eight valence electrons, some shared in bonds.

In this structure, the carbon atoms shares one of its valence electrons with each hydrogen,

and each hydrogen shares its single electron with carbon to make a compound with a complete valence shell.

In the blue-hilighted box below, the central carbon is surrounded by a complete octet of eight electrons, and each hydrogen has its capacity, two electrons, by sharing electrons.

Two electrons between atoms indicates a single bond, which can be rewritten, as on the right, by a single bar.

methane lewis structure


Example 2: Ammonia, NH3

Ammonia is NH3. Nitrogen has five valence electrons and each hydrogen brings one to the molecule. It's easy to see that those three electrons from the hydrogens could complete an octet on the nitrogen: 5 + 3 = 8.

There's a twist in this molecule—a small one—and it gives ammonia some startling properties, some of which are beyond the scope of these notes, but trust me, they're cool.

The figure below shows how to construct the Lewis structure. Start with each atom surrounded by its valence electrons, 5 for N, 1 for H. I like to color each atom's electrons differently so I can keep track of them, but it's not absolutely necessary.

Arrange the atoms by trial and error (and intuition that you'll develop with enough practice) to get a structure in which the sharing of electrons completes the valence shells of all atoms. That's the most likely way the molecule will bond.

One of the pairs of electrons on the nitrogen of ammonia is not bonded. We call that a lone pair. It occupies its own stable orbital, as shown in the stick diagram on the right.

Lewis structures

Lewis structures tell us about the most-likely bonding arrangement and bond types of molecules, but they tell us little about the structure - the 3D shape of the molecule. For that we'll need other skills.

Example 3: Water, H2O

Water is a very important molecule, so it's important to understand its bonding, which will in turn create all of its other properties.

The Lewis structure of water shows that the oxygen atom has two lone pairs.

Those lone pairs, together with the large difference in electronegativity between oxygen and hydrogen, give water one of its most important properties, its strong polarity.

In the rendering on the right below you can see that water, which actually is a bent planar molecule (again, you wouldn't necessarily know this just from the Lewis structure), has a negative end and a positive end.

More correctly, it has one end that is more negative than the other (called δ-) and one more positive (called δ+). The unbonded electron pairs create a region of dense negative charge. And because oxygen holds the bonding electrons of the H-atoms tightly to itself, the H-atoms are essentially bare protons hanging off the oxygen.

The polarity of water and its ability to hydrogen bond gives water some of the properties that are deeply intertwined with the chemistry of living things on Earth. It's for that reason that it's difficult for us to conceive of life on another planet without water – but you never know ...

water Lewis structure


Example 4: Double & triple bonds

Lewis structures can show us when double and triple bonds are most likely, or perhaps the only kind of bonding that make a molecule possible. Here are some Lewis structures that contain double and triple bonds (and indeed the real molecules do, too).

The double bonds in carbon dioxide, CO2, are what make it a linear, non-polar molecule, and that structure, in turn, gives it most of its properties.

CO2 solidifies, for example, at about -57˚C, and the liquid only exists if the gas is placed under about 5 atmospheres of pressure. The triple bond of nitrogen gas, N2, is very strong. Although our atmosphere is mostly nitrogen in the form of N2, most organisms on Earth can't use it in that form because they can't break that bond. They require other sources of the crucial element.

CO2 Lewis structure


Example 5: Degeneracy

Some Lewis structures will lead to bonding that is ambiguous. A double bond might be present between an atom and one or more other equivalent partners. Which one to choose? This is called a degeneracy, and it turns out that nature tends to pick both, neither, and a combination of the two bonds.

As an example, let's look at the Lewis structure of nitric acid, HNO3. First the atoms with their valence electrons:

example 5 equation 1

Now we can arrange the bonds in two ways. In both, all atoms have a full valence shell. Here they are:

example 5 equation 2

Take a minute and convince yourself that every atom (except the hydrogen) has an octet of electrons in its valence.

Here are the two structures in stick form:

example 5 equation 3

So which one does nature pick? Well, it turns out that whenever we have two equivalent structures like this (we have two degenerate structures or a degeneracy), nature picks a combination of both, and we're better off writing the two bonds more like 1-1/2 bonds, like this:

example 5 equation 4

Notice that the red oxygen is different than the other two. It's bound to a hydrogen and the electronegativity difference makes this bond more ionic than covalent. The result is that the hydrogen can detach as a bare proton quite readily, leaving a NO3- ion behind. That's why HNO3 is an acid.


Example 6: Carbonate ion, CO32-

Now let's see how a molecular ion, the carbonate ion, CO32-, can bond stably. When we work with ions, we begin with the usual number of valence electrons of a neutral molecule, in this case four for carbon and six for each of the three oxygens. But this is a 2- ion, so we'll add two electrons to the neutral mix to give it that -2 net charge.

Those last two electrons can be filled in anywhere they're needed to form a full valence. We start with the raw materials:

example 6 equation 1

Now put them together and use the two extra (red) electrons to fill in any gaps in order to form full valence shells for every atom.

example 6 equation 3

Finally, notice that this is another degenerate structure. There are two other equivalent places to put our double bond, like this:

example 6 equation 4

In this case, the reality is that each C-O bond is equal, stronger than a single bond, but weaker than a double bond. We might write the structure of CO32- like this:

example 6 equation 5

Here I've left off the lone pairs of the oxygen atoms. There might be a context in which we'd want to show those, but most of the time it's quicker to omit them.


Molecular ions

Many molecules for which stable valence shells cannot be built from the number of electrons present on the neutral atoms that compose them can be made stable if electrons are lost are gained. These are molecular ions.

Some important molecular ions are OH-, NH4+, SO42-, PO43-, CO32-, COO-   &   CN-


Example 7: Sulfate ion, SO42-

The sulfate ion, SO42-, is a very interesting exception to many of our assumptions about bonding. In fact, it caused a lot of argument in the chemistry community early on. At first glance, with sulfur and oxygen both holding six valence electrons, we might draw a Lewis structure like this:

sulfate figure 1

The problem is that the two extra charges needed to stabilize this molecule are localized on the sulfur atom. Nature tends to spread that extra charge out, and sometimes at a cost that can contradict what we've already learned. In this case, it's the octet rule. In fact, SO42- tends to bond more like this:

sulfate figure 2

Now the extra charges are a little more spread out, and we can see that there's nothing special about our double bond locations, which means resonance structures and even more spreading of charge. But the twelve electrons around the sulfur are troubling. Remember that sulfur has d-electrons, and some of those are used as valence electrons.

Overall this structure is more stable than the all singly bonded one.

Here are all of the resonance forms of SO42-, and they lead to an ion with four identical bonds that are somewhere between double and single in strength.

sulfate figure 3

It was a measure of the S-O bond length in SO42- that led to a deeper investigation of the bonding.

You shouldn't feel like you ought to have recognized this case. It took some Nobel-prize winning chemists, including Linus Pauling, some time and significant argument to uncover the truth. It says a lot about the nature of the electron, if you think about it.

Some other exceptions

The sulfate ion (above) is one case of an exception to the octet rules. There are others. I'm not sure there's any point in memorizing such exceptions; better to know that they exist and be wary of them. Know some of the signs that an exception might exist. Here are a few examples.

Phosphorus pentachloride, PCl5

Phosphorus pentachloride (PCl5) is an exception to the octet rule. You can see the Lewis structure of PCl3 in the practice problems below. Because a chlorine atom only needs one electron to complete its valence shell, it shares one and only one electron with phosphorus, so in PCl5, phosphorus is surrounded by a total of ten electrons. It does this by using its d-shell electrons.

PCl5 structure

A more 3-dimensional structure is shown on the right. Three chlorines are in a plane (blue triangle) and the line containing the other two cuts through the center of that triangle and is perpendicular to it. The arrangement is called a trigonal bipyramid.

Sulfur hexafluride, SF6

For similar reasons, sulfur can bind to six fluorine atoms with single bonds in a square bipyramid arrangement.

SF6 structure

Xenon hexafluoride, XeF6

Finally, we don't normally think of noble gases interacting with anything, let alone forming bonds. But it turns out that if the noble gas is big enough, like xenon (Xe), the d-orbitals can allow bonds to form. Xenon forms a couple of covalent compounds, one of which is XF6.

XF6 looks just like SF6, but the central Xe is now surrounded by 14 electrons.

XeF6 structure

Practice problems

Roll over the boxes to see the answers - but not before you've tried it yourself!

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