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my arrows are wrong, can i get help on that
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- Please draw the conjugate base for each below as indicated in the picture below and offer a detailed explanation. Thank you so much.Curved arrows are used to illustrate the flow of electrons. Using the provided resonance structures, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond-making steps.Consider the following bases: a. For each base above, circle the atom/atoms with the highest PE (will release the most P.E.when a lone pair on this atom combines with an H+ ) b. Rank the bases 1 (highest P.E./strongest base) to 7 (lowest PE/weakest base), and explainyour reasoning.
- Kindly explain why COSe is the answer in detail.Use Huckel’s rule to identify if its aromatic or not. Draw the resonance structure of the ff. compounds. note: I need the answer immediately. I will send a good rate right away as well.Please draw the arrow formalism on the 1st structure (top) that accounts for the 2nd resonance structure (bottom).
- Please draw a step by step arrow pushing mechanism. Make it very detailed and include all arrows and include ALL resonance structures.Which of the following resonance structures has the greatest contribution to the hybrid? Explain.Draw the resonance structure of the ff. and identify if aromatic or nonaromatic through Huckel’s rule. note: I need the answer immediately. I will send a good rate right away as well.