Q1. The curved arrow mechanism below has not been completed. What is missing are curved arrows and formal charges. Your task is to complete the mechanism with all curved arrows and formal charges.. OH HO. HO HO. H. >
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- Mechanism, please show arrows and intermediates and formal charges so I can keep along and understand how you did it and learn it hopefully.Could you put them each in order from "Most electrophilic to the Least electrophillic? Thanks!Please draw the arrow formalism on the 1st structure (top) that accounts for the 2nd resonance structure (bottom).
- I'm looking for an alkene with a single methyl group and an anti markovnikov Br at the last carbon and the markovnikov with Br on the bottom. The image is attached is just to illustrate positioning of the Br, and not an actual alkeneBuild a model of methylcyclohexane, and use the model to complete the following Newmanprojections of methylcyclohexane in the chair conformation: a. When the methyl group is in an axial or equatorial (circle one) position, the molecule is inits lowest potential energy conformation. b. Label one Newman projection above anti and the other gauche to describe the relationshipbetween the methyl group and C3 of the ring. c. In general, which is a lower PE conformation, anti or gauche? d. Explain how your answer to b and c provide an explanation for why it is more favorable fora large group to be in an equatorial than an axial position.Please help with row 3 highlighted in yellow (column 1 and column 2); the instructions for the specific column in row 3 are above row 1: Follow the instructions in each column. Hint for the last column: draw it with a wedge and again with adash – which gives the correct configuration?
- Step 1c: Draw the structure(s) resulting from the curved arrow mechanism of step 1. Include formal charges and all hydrogen atoms, but do not include lone pairs.Rewrite the entire reaction in Full Structure Format with the Ending Products [The second image is an example of Full Structure Format ] THANKSSSSSSSSSSSSI already have the degrees of unsaturation (question 1) and just need 2 and 3