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draw an 8 membered ring that would be considered anti-aromatic. include the molecular orbital diagram derrived from frosts circle
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- Circle aromatic compound(s)Characterizing a Compound as Aromatic, Antiaromatic, or Not Aromatic Label each compound as aromatic, antiaromatic, or not aromatic. Assume all completely conjugated rings are planar.Label each compound as aromatic, antiaromatic, or not aromatic. Assume all completely conjugated rings are planar.
- Determine whether the following molecules are aromatic (A), non-aromatic (NA), or anti-aromatic (AA), and show the use of a Frost circle in determing aromaticity. You may assume planarity.Which compound is not aromatic? A. only A and D B. A, B and C C. only B D. only Aexplain whether A,B, C and D are aromatic, anti-aromatic or non-aromatic
- Cyclooctatetraene is a not planar because it disrupts conjugation and avoids anti-aromaticity. b planar because it ensures conjugation and allows anti-aromaticity. c not planar because it disrupts conjugation and avoids aromaticity. d planar because it ensures conjugation and allows aromaticity.AZT was the rst drug approved to treat HIV, the virus that causes AIDS. Explain why the sixmembered ring of AZT is aromatic.what aromatic annulene has the same number of bond molecular orbital as the hypothetical all cis (20) annulene
- Are the following molecules aromatic, antiaromatic, or non-aromatic? Why?Which of the following statements is FALSE? Select one: a. Aromatics are compound that are conjugated. b. The Cs and Hs in an aromatic compound are equivalent. c. The pi electrons are delocalized around an aromatic ring. d. None of the statements is false.Add electrons to your energy diagram to show the configuration of the cyclopropenylcation and the cyclopropenyl anion. Which is aromatic and which is antiaromatic?
