Molecules Structure as Planar Graphs?

In summary: Kuratowski's theorem says that every nonplanar graph contains either a topological K5 or a topological K3,3. In other words, for an organic molecule to be non-planar, you have to either have:1. Five carbon atoms such that there is a chain (of bonds and atoms) from each one to each of the others, with none of these 10 chains sharing any bonds or atoms with any of the others; or:2. Two sets of atoms of valence 3 or more, such that there is a chain from each atom in the first set to each atom in the second set, with none of these 9 chains sharing any bonds or atoms with any of the others.To
  • #1
LarryS
Gold Member
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I have read that the structure of almost all organic molecules can be represented visually as Planar Graphs, i.e. 2-dimensional lattice-like structures consisting of nodes (points) connected by lines in which no lines cross. From the perspective of Physical Chemistry, does anybody know why this is so? Some graphs are of such complexity that they required 3 dimensions to guarantee that no lines cross - reference "3 Utilities Puzzle".
 
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  • #3
mathman said:
https://www.google.com/search?q=eth...PLNdKwsAT85oDYCg&ved=0CC8QsAQ&biw=943&bih=672

It is a simplification for showing on a sheet of paper. The above shows that something as simple as ethane has a three dimensional structure.

Yes, actually, I was referring to the "simplification for showing on a sheet of paper" rather than to the structure in real 3D space. For most organic molecules, it is possible to represent the topological relationship of the atoms and their connections via covalent bonds on a 2D "surface" - on a plane or on a sphere. From what I have read, organic chemists do not know why this is so.
 
  • #4
Because most organic molecules do not have the degree of interconnectedness required to be non-planar.

Kuratowski's theorem says that every nonplanar graph contains either a topological K5 or a topological K3,3. In other words, for an organic molecule to be non-planar, you have to either have:

1. Five carbon atoms such that there is a chain (of bonds and atoms) from each one to each of the others, with none of these 10 chains sharing any bonds or atoms with any of the others; or:

2. Two sets of atoms of valence 3 or more, such that there is a chain from each atom in the first set to each atom in the second set, with none of these 9 chains sharing any bonds or atoms with any of the others.

To satisfy either of these conditions, you need a lot of high-order carbons and a lot of different paths between them. That would require a large and highly interconnected molecule. But it's by no means beyond the realm of possibility, and I have to imagine that some proteins, with their abundant disulfide interconnections, are non-planar (containing K3,3). It also seems like some people have synthesized non-planar molecules intentionally: see this article, for example.

EDIT: After posting I found this article which discusses the issue further. The author seems to have a bit of confusion between nonplanarity and knottedness (you can have a knotted molecule that has a planar graph), but apart from that the analysis seems good.
 
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  • #6
Of course there are molecules where this is not true, e.g. adamantane.
The problem with this kind of question is which metric to use:
All organic molecules with a CAS number? All possible organic molecules with, say, up to 100 C atoms?
 
  • #7
referframe said:
I have read that the structure of almost all organic molecules can be represented visually as Planar Graphs, i.e. 2-dimensional lattice-like structures consisting of nodes (points) connected by lines in which no lines cross. Does anybody know why this is so? Is it due to the properties of covalent bonds?

There is a grain of truth in that, while I think I can imagine some examples of molecules that we won't be able to reproduce this way, most molecules I can think of are "topologically flat" (with all possible disclaimers about them being in fact 3d).

No idea about explanations. And I am not convinced they are strictly chemical.

Ygggdrasil said:
Adamantane comes to mind as a molecule for which this does not appear to be true.

DrDu said:
Of course there are molecules where this is not true, e.g. adamantane.

Sorry guys, that's incorrect. Adamantan can be drawn flat - hint.
 
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  • #8
Borek said:
Sorry guys, that's incorrect. Adamantan can be drawn flat - hint.

Gotcha! It is K4, not K5.
 

1. What is a molecule structure as a planar graph?

A molecule structure as a planar graph is a visual representation of a molecule where the atoms are represented as vertices and the chemical bonds between them are represented as edges. This type of graph is a simplified way to understand the connectivity and arrangement of atoms in a molecule.

2. Why is a molecule structure represented as a planar graph?

Molecule structures are often represented as planar graphs because they provide a simplified and easily understandable visual representation of the molecule. Additionally, planar graphs allow for the prediction of molecular properties and reactions based on the arrangement of atoms and bonds.

3. How do you determine the connectivity of atoms in a molecule using a planar graph?

The connectivity of atoms in a molecule can be determined by looking at the number of edges connected to each vertex (atom). This number corresponds to the number of chemical bonds that atom has with other atoms in the molecule. For example, a carbon atom with four edges connected to it would have four chemical bonds with other atoms.

4. Are there any limitations to representing a molecule as a planar graph?

Yes, there are limitations to representing a molecule as a planar graph. Planar graphs do not account for the three-dimensional structure of molecules, which can play a significant role in their properties and reactions. Additionally, planar graphs may not accurately represent molecules with complex structures or multiple bonding patterns.

5. How can planar graphs be used in chemistry?

Planar graphs are widely used in chemistry for a variety of purposes. They can help chemists predict the reactivity and properties of molecules, identify isomers (molecules with the same chemical formula but different structures), and design new compounds with desired properties. They are also useful in teaching and visualizing the structures of molecules for students.

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