Chem3x11 Lecture 1
Being constructed (Apr 14) - not yet finished.
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- Cycloalkanes have 3D structure
- Cyclohexane has a chair conformation and a less stable boat conformation
- Dynamic movement of cyclohexane causes "ring-flipping" which swaps axial and equatorial substituents
Basic Types of Cycloalkanes
Cycloalkanes are, as might be expected, cyclic alkanes, with general formula CnH2n, with a logical naming system:
Naming Substituted Cycloalkanes (revision from Y1)
The nomenclature is like any other organic molecule:
...and you name the molecule right to left. i.e. stem (parent) first, then the subsituents, then the stereochemistry. Let's try one:
The parent ring is cyclohexane. There are two methyl groups hanging off the ring, and we have to specify unambiguously where they are. Take one of them as number "1" and number the other atoms around the ring in order, keeping the numbers as low as possible, i.e.:
The stereochemistry is cis because the two methyls are on the same face of the ring (coming towards us). Remember that cis and trans isomers can only be interconverted by breaking bonds - they are configurational isomers.
So the full name of this molecule is cis-1,3-dimethylcyclohexane. We write the name left to right, but we devised the name right to left.
Why Cycloalkanes Aren't Flat
sp3 carbon likes to bond with angles of about 109°. If we look at cycloalkanes (they way we draw them on paper), we see that there is a problem - the structures must be strained.
The angle strain for each of the above structures would be 49°, 29°, 1° and 11° respectively. Does this correspond to reality? No, because molecules are not flat. In reality cyclohexane has zero angle strain because it buckles out of the plane and ends up looking like a chair (sort of). We call this the chair conformation. The ring can actually adopt all kinds of shapes, but the global minimum energy is this chair conformation.
There's another conformation that is often seen, but which is higher in energy, and that's the boat conformation:
Despite the freedom to buckle and move, remember that rings have far less conformational freedom than their acyclic counterparts.
Axial and Equatorial Substituents on Cyclohexane
This may seem like an art class, but it's very important to be able to draw groups attached to cyclohexane. The first thing to get right is the ring itself. Let's start with the chair conformation, below. Now if we want to draw cyclohexane from the top, we just draw a regular hexagon, but if we want to indicate its real 3D shape, we draw it from the side:
Notice the way each line is parallel to another. And that some of the vertices actually lie on the same imaginary horizontal line. If we actually model cyclohexane on a computer (or build a model in our hands) it looks like this:
You'll notice the substituents are of two types - ones that stick up/down vertically, and others that appear initially to be at odd angles. Let's look at these in turn.
These H's are all equivalent in cyclohexane. We draw the bonds vertically. Notice how they alternate between up (when the ring points up) and down (when the ring points down). Notice how we break the line indicating the C-H bond at the back, to show that it's at the back.
These substituents point out from the ring. Notice how the lines are parallel to a C-C bond one bond away.
The convention is that if we draw a cyclohexane flat, we're viewing it "from above". It's important to see how the stereochemistry we draw with wedged and dashed bonds translates into 3D:
...i.e. substituents that are "up" in the usual representation on the right in the scheme above are not necessarily axial. We'll come to this in more detail when we talk about how the ring moves.
The Boat Conformation of Cyclohexane
While cyclohexane's chair conformation has two different kinds of hydrogen atom environments, the boat conformation has four. The clash shown below helps explain why the boat conformation is less thermodynamically favoured.
Why the Chair Conformation is Preferred
As we can see from Scheme 13 there is a steric clash in the boat conformation. That's not all. There is another kind of strain. It's not angle strain - all the bonding angles in either the chair or the boat are 109°. It's a torsional strain. To see this we can draw Newman projections of the two conformations, like this:
Notice the eclipsed C-H bonds in the boat conformation - this causes the torsional strain. The overall effect of the combined torsional and steric strains are that the boat conformation is higher in energy than the chair by 24 kJ mol-1.
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