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How would you draw the resonance structure for the compound below:

enter image description here

This is one of the resonance forms I think... but I'm sure there is another one too.

enter image description here

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The resonance structures and how to construct them for 3-aminocyclohex-2-en-1-ylium are shown below. The second structure in your question is none of them, as it is a different molecule: cyclohexa-1,3-dien-1-amine. For this molecule it is also possible to construct a resonance structure, as also shown below.
resonance structures
However, the two structures can be interconverted via an acid-base reaction.


And for the stability of 3-aminocyclohex-2-en-1-ylium, the last structure would be most stable (with the positive charge on the EN nitrogen)?

There is no such thing as a most stable resonance structure. Resonance is only a concept that breaks down a highly complicated electronic structure into imaginable contributions of Lewis structures. All of these contributions are present all of the time. However, there are usually a few, that would describe the overall character best. Sometimes there is even only one predominant one.
The concept of resonance is necessary to describe delocalisation effects, hence the Lewis-like representation below is probably much closer to the actual structure than any of the resonance forms depicted above.
delocalised structure

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  • $\begingroup$ And for the stability of 3-aminocyclohex-2-en-1-ylium, the last structure would be most stable (with the positive charge on the EN nitrogen)? $\endgroup$ – liya77 Apr 21 '15 at 5:00
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    $\begingroup$ @liya77 Please see my edit. $\endgroup$ – Martin - マーチン Apr 21 '15 at 5:24

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