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Are these Anti aromatic/aromatic or non aromatic?

1.

1,1'-bi(cycloprop-2-en-1-ylidene)

Here, if we were to consider the resonating structure(s) with charge separation

One ring is aromatic and other is anti aromatic, and secondly there is not continuous delocalization of pi electrons between those rings {if we don't include no resonating structures with no formal charges, as their contribution would not be equalish to normal form} what category would this go in?

2.

1,4-dioxine

Like before, there can be no continuous electron delocalization like stated in previous example , only other ones the diff forms of

If we consider it to have enough delocalization, it would have 4n electrons and hence antiaromatic {although all the orbitals wont be mixed as 3 on each side twice with oxygen's lone pair being common between all of them}

  1. As we can see in pyrene, if we consider central double bond to be non participating, huckle rule works, is there a better (and just by observation by eye) method that we could use for multi ring systems? what is the basic condition for aromaticity besides planar,cyclic,sp2 {nitrogen and oxygen in general change their hybridisation as to make it aromatic with their lone pair(s)}
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  • $\begingroup$ What is the question? $\endgroup$ – Lighthart Feb 4 '16 at 22:19
  • $\begingroup$ is the second one aromatic or not? and if there is a better way to evaluate aromaticity $\endgroup$ – Mrigank Feb 4 '16 at 22:28
  • $\begingroup$ The second one is definitely not aromatic. It would have 4n electrons if planar; the oxygens would need to be sp2 hybridized to make this molecule planar, meaning there would be a lone pair in a p-orbital each $\endgroup$ – Lighthart Feb 4 '16 at 22:39
  • $\begingroup$ i mean anti aromatic or not $\endgroup$ – Mrigank Feb 4 '16 at 23:33
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Antiaromaticity is a fictional state with real consequences, that any molecule will distort to avoid.

In the case of molecule 1, the primary state will be a triplet (unpaired pi-electrons), with the central bond lengthening to decrease the pairing of the pi-electrons. This will lead to 3 electrons in each pi-system, and hence preventing antiaromaticity, because there are no longer 4n electrons in the rings. A fictional molecule, with the constituency shown for molecule 1 that is in a singlet state would be antiaromatic.

In the case of molecule 2, the molecule will distort itself to make the at least one of the oxygens non-coplanaer with the pi-system, and no longer being co-planar, the system will not be antiaormatic. A fictional molecule with the constituency shown for molecule 2 that is co-planar, would be antiaromatic.

It is unclear what you are asking about for pyrene.

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  • $\begingroup$ ok, understood, would the same happen ![](i.gyazo.com/81dd8367e76467c1822d748ab67b464e.png) here? $\endgroup$ – Mrigank Feb 4 '16 at 23:54
  • $\begingroup$ Yes, and the net effect is that the 2-proton in 2-H pyran is basically undeprotonateable. $\endgroup$ – Lighthart Feb 5 '16 at 0:41
  • $\begingroup$ Wouldn’t molecule 1 also distort so that the two rings are perpendicular to each other? $\endgroup$ – Jan Jan 31 '17 at 0:25

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