mundane Posted August 8, 2020 Posted August 8, 2020 why is the compound non aromatic despite it having resonance?
hypervalent_iodine Posted August 8, 2020 Posted August 8, 2020 Having resonance doesn't mean something is aromatic, you also have to have a fully conjugated system. Have you drawn out the resonance structures?
studiot Posted August 8, 2020 Posted August 8, 2020 Look here at the 'four rules' https://www.masterorganicchemistry.com/2017/03/03/is-this-molecule-aromatic-some-practice-problems/ Quote Our last post in this series on aromaticity went through the 4 conditions a molecule must fulfill in order to be aromatic. First, it must be cyclic Second, every atom around the ring must have an available p-orbital Third, the number of electrons in the pi system must be 2, 6, 10, 14, 18, or a higher number in the set that increases from 18 in increments of 4 (22, 26, 30…. etc). We usually abbreviate this as [4n+2] pi electrons. Fourth, the molecule must be flat. In that post we tried to explain what each of those rules meant – so if any of these individual items seem unclear to you, it might be a good idea to go back to that post. In this post,we’re going to apply these 4 rules with some practice examples. Look down the examples to cyclobutene (could you name your compound ? ) Can you find a cyclobutene that is aromatic?
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