Tuesday, September 8, 2009

Dipole-Dipole Forces

Do you remember how electronegativity works? I posted about it, so you should. Here, just for you, I'll link back to that post. Electronegativity is necessary to understand polarity. And polarity is how these forces operate. An organic molecule with a functional group that contains an electronegative atom such as oxygen or nitrogen will likely have a permanent dipole. The heteroatom pulls negative charge toward itself (because it's electronegative, obviously). As described in the previous post, regions of the molecule can have differential charge. But a permanent dipole is much stronger than the fleeting changes responsible for London dispersion. Because of this, molecules that have dipole-dipole interaction experience stronger intermolecular forces than ones that have only London dispersion. Compounds with this property are said to be polar and ones that do not are non-polar. Consider these examples...

Acetone
Condensed structure: OC(CH3)2
It has a permanent dipole that looks like this.
Those Greek letters represent partial charge. The electronegative oxygen pulls electron density toward itself, so it is the center of negative charge. The region opposite it, lying near the central carbon, is the most positively charged region of the molecule.

Carbon dioxide
Condensed structure: CO2
This time, when we draw the arrow through one oxygen, the other oxygen cancels it out. Despite having a highly electronegative element, carbon dioxide is non-polar.

Whether a solvent is polar or non-polar tells chemists a lot about its potential uses, and some reactions need one type of solvent or the other. Acetone is a well-known polar solvent, but water is the best known in this category. Many organic compounds such as n-hexane are commonly used as non-polar solvents. That's all for these at the moment. Just remember that in order for dipole-dipole forces to occur, the compound(s) must have permanent dipoles, and that dipole-dipole forces are usually much stronger than London dispersion. Of course, a molecule can have both. But the stronger forces are considered to override the weaker ones for all practical purposes that I've encountered.

3 comments:

  1. i am a 'non-traditional' student (read "older"), returning to school for a biology degree and masters in ed. i'm loving your posts...seems we must be reading from the SAME text book. i do appreciate your time involved in putting this together. its been a while...i'm sure you are busy. just wanted you to know it is greatly appreciated!

    ReplyDelete
  2. I'm not so much "busy" as I am lazy. I feel bad about this but only a little, since not too many people make blog posts about sections in their organic chemistry textbooks at all, let alone infrequently.

    As for getting a biology degree and a masters in education, that is very good. The world sorely needs more teachers who understand science and can communicate scientific principles.

    I'm sure there's lots of overlap between organic chemistry textbooks, but the one I have is Janice Gorzynski Smith's.

    Thanks for the support. Also, don't be put off by the acerbic tone I sometimes use in my posts here. I just have a bizarre sense of humor.

    ReplyDelete
  3. Great post and information about electronegativity, it is a recall to the things we knew about that. Thanks for sharing this! I am sure that this will help a lot the people who are looking for a topic like this. Thanks.

    Polar organic solvents

    ReplyDelete