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Organic 8 Online
OpenStudy (lbarrientos1):

I can't seem to understand electron movement in resonance. does it follow a specific pattern?

OpenStudy (anonymous):

Yeah definitely it does. It would be great if you had a specific example so I could show you and clear it up for you. But if not, I can come up with some examples of my own.

OpenStudy (lbarrientos1):

I had one but I can't seem to find it...

OpenStudy (anonymous):

That's fine, are you looking at an uncharged molecule, and what kinds of elements are you comfortable with like carbon, nitrogen, oxygen, all being in resonance? Like specifically what functional groups or types of things would you like to see in whatever example I make up, I don't wanna freak you out too bad with some weird stuff haha

OpenStudy (lbarrientos1):

I honestly can't remember. All I know is that it was an aromatic hydrocarbon. Most likely benzene, but I don't remember anything else

OpenStudy (lbarrientos1):

I will look for the paper one more time...

OpenStudy (lbarrientos1):

|dw:1442722763174:dw|

OpenStudy (anonymous):

Ahh alright perfect example for me to play with, also sorry I was away for a few minutes. Now I'll go ahead and write out some resonance structures and then I'll explain them. |dw:1442723355192:dw| The most important rule of drawing these arrows is that you MUST start your arrow at electrons. So in this case I am starting them from a bond, and a bond is just electrons between atoms, so I'm allowed! Other than bonds, the only other place you'll find electrons are in lone pairs. Here I moved electrons from the double bond to shift the 2 electrons over to the other bond. Since electrons are negative, they canceled out the positive charge from the new place they moved to, but they left a positive charge behind. We can reverse this back and forth if we like. Perhaps this Lewis structure will help to show where the electrons moved. |dw:1442723693384:dw| Generally speaking you won't break a sigma bond, only pi-bonds which are what make up double and triple bonds. So you won't be breaking any single bonds this way, well at least not at the moment, but it is possible. I feel like I might be saying quite a bit too much so I'll try to make it a little less complicated, and end with drawing out how to get to the last resonance form and then you can ask some questions. |dw:1442723899977:dw|

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