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For NO3-, are all the Os equivalent? Experiments say that the actual C-O bond lengths are the same, how does that fit in? Resonance is one of those things that I never really understood until organic chemistry. Gen Chem 1 gave a brief introduction, and gen Chem 2 had a few more things to add, but it was never really useful.

Then orgo comes along and now it's one of the most important concepts and you realize how simple it is! The important thing to realize about resonance forms is that they are not necessarily different structures, but they all together defime what a molecule truly looks like!

When a compound has a formal charge at a certain location, we indicate that with a plus or minus symbol at that atom. If the compound had resonance forms then this is not really an accurate image. Instead, that charge is said to be stabilized by resonance! Meaning that electron density is truly spread out among the different resonance structures! If this is going over your head, don't panic!!

This is truly fascinating stuff, but you won't have to understand it in such detail for a while yet. Just understand that resonance forms are not really separate structures, but if you were to impose them on top of one another they would paint a more accurate picture of how that molecule truly exists! Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

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To view LaTeX on reddit, install one of the following: Custom superscript and subscripts: Welcome to Reddit, the front page of the internet. Become a Redditor and subscribe to one of thousands of communities. HomeworkHelp submitted 4 years ago by ooglebooo. How can I tell? Want to add to the discussion? Draw them and see. Draw one, that looks good.

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