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Chem3x11 Lecture 1

Being constructed (Apr 14) - not yet finished.

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Key concepts

  • 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

Cycloalkanes

Basic Types of Cycloalkanes

Cycloalkanes are, as might be expected, cyclic alkanes, with general formula CnH2n, with a logical naming system:

Scheme 1: The Names of Simple Cycloalkanes
Scheme 1: The Names of Simple Cycloalkanes

Naming Substituted Cycloalkanes (revision from Y1)

The nomenclature is like any other organic molecule:

Scheme 2: Basic Naming Convention for Most Organic Molecules
Scheme 2: Basic Naming Convention for Most Organic Molecules

...and you name the molecule right to left. i.e. stem (parent) first, then the subsituents, then the stereochemistry. Let's try one:

Scheme 3: Example Substituted Cycloalkane to Name
Scheme 3: Example Substituted Cycloalkane to Name

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.:

Scheme 4: Numbers are Kept Low in Molecule Numbering
Scheme 4: Numbers are Kept Low in Molecule Numbering

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.

Scheme 5: If Cycloalkanes were Flat, there would be Strain
Scheme 5: If Cycloalkanes were Flat, there would be Strain

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.

Scheme 6: Cyclohexane's Chair Conformation
Scheme 6: Cyclohexane's Chair Conformation

There's another conformation that is often seen, but which is higher in energy, and that's the boat conformation:

Scheme 7: Cyclohexane's Boat Conformation
Scheme 7: Cyclohexane's 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:

Scheme 8: Drawing Cyclohexane's Chair Conformation, Ignoring Substituents
Scheme 8: Drawing Cyclohexane's Chair Conformation, Ignoring Substituents

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:

Scheme 9: What Cyclohexane Really Looks Like
Scheme 9: What Cyclohexane Really Looks Like

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.

Axial Substituents

Scheme 10: The Axial Hs on Cyclohexane
Scheme 10: The Axial Hs on Cyclohexane

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.

Equatorial Substituents

These substituents point out from the ring. Notice how the lines are parallel to a C-C bond one bond away.

Scheme 11: The Equatorial Hs on Cyclohexane
Scheme 11: The Equatorial Hs on Cyclohexane

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:

Scheme 12: The Correspondence Between Different Ring Representations
Scheme 12: The Correspondence Between Different Ring Representations

...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.

Scheme 13: The Hydrogen Environments in Cyclohexane's Boat Conformation
Scheme 13: The Hydrogen Environments in Cyclohexane's Boat Conformation

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:

Scheme 14: Newman Projections of Cyclohexane's Chair and Boat Conformations
Scheme 14: Newman Projections of Cyclohexane's Chair and Boat Conformations

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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