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- For each proposed set of resonance structures: a. (E) Add curved arrows (starting from left) to show how each successive r.s. was generated. b. Cross out any resonance structures that are NOT important, and explain your reasoning.Could you put them each in order from "Most electrophilic to the Least electrophillic? Thanks!pls correct me if im wronginstruction: Match rows in columns based on the chemical reactions of benzene
- Why was the formal charge of (+) placed on this carbon? I understand everything else about the question but can someone help me with explaining this. Thanks!I need alot of help on this section too!!The last part of the question asks to draw product, including non bonding electrons and formal charges. I don't understand what I've been doing wrong so any help would be great! Thank you!
- provide well-explain asnwers for the following; -)When the H dissociate from hydroxyl, the rest with different structures who can maintain the negative charge of O most ? Primary, Secondary, Tertiary. -)If the carbon connect with one or more chlorine, how about the new structure's ability to maintain negative charge ? Stronger, weaker -)Comparing the carbon connect to chlorine or fluorine, which halogen can enhance this ability ? Chlorine, Fluorine, they play same( give clear handwritten dont copy previous ans )Rewrite the entire reaction in Full Structure Format with the Ending Products [The second image is an example of Full Structure Format ] THANKSSSSSSSSSSSS