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- For the molecule below is the ring (as shown – the particular resonance form drawn) aromatic, why or why not? Using correct arrow-pushing convention, show the formation of a resonance form of the above structure that is aromatic. What is the charge of the five-membered ring in the main contributing resonance form?Tell whether each compound as aromatic, nonaromatic, or antiaromatic. Give explanation.Consider the aromatic anions below and their linear counterparts. Draw all of the resonance forms for each. What patterns emerge?
- The curved-arrow convention depicts the flow of electrons, including bond-forming and breaking events. Draw the outcome of the following reaction based on the provided curved arrow. Be vigilant regarding formal charges. :ci: B. Ci: Draw three additional resonance structures of acetamide (below) and use curved arrow notation to show how the resonance structures are formed. Label the resonance contributors alphabetically (ex. A, B, C, D) and rank them from most to least significant contributor. •oº• Ⅱ. H3C 0°• H N HCompound b is more polar than A. Explain. (Hint: draw resonance structures)Rank the molecules in decreasing (strongest to weakest) acidity. Include ALL resonance structures with arrows and explain reasoning for rank.