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Aug 27, 2020 at 2:12 vote accept Master Maxx
Sep 4, 2020 at 5:35
Aug 13, 2020 at 11:04 comment added user96208 pubs.acs.org/doi/10.1021/ja00168a059
Aug 13, 2020 at 10:29 comment added user96208 Unfortunately I do not have the time to compile resources as of now and present a full sourced answer. I only pointed out the incorrectness of your assumption using available NMR analysis, which maybe edited appropriately. As a valuable resource, you can just read about how NMR points at aromaticity and alkene nature, that will also be beneficial to point out the inaccuracy without computational/Lab analysis.
Aug 13, 2020 at 10:10 comment added Safdar Faisal @AnindyaPrithvi If that is the case, you could submit your own answer and prove this is wrong. Unfortunately, I am currently short of such resources as you state and if a substantial proof can be given, I would be more than happy to upvote it. I stated It would be more prevalent as similar to cyclobutadiene it seems to behave more as an intermediate than be present as a compound. And so assumed it would be more antiaromatic than aromatic. There may be flaws centered around my lack of complete knowledge, so as I said above please formulate your answer. Thanks for your concern regarding my ans.
Aug 13, 2020 at 9:17 comment added user96208 Reading this you cannot say it's dominating the aromaticity. The NMR calculations referred in the book shows the alkene like character at cyclobutadiene promoting Diels Alder. You've manipulated the statements well. FYI, Cyclobutadiene can be NON aromatic as well depending on the adopted geometry. As a member of 21st century you may perform the calculations yourself at any chem-computer and find the aromaticity of phenyl ring and alkene-city of cyclobutadiene
Jul 23, 2020 at 11:19 history answered Safdar Faisal CC BY-SA 4.0