2. Write "most" under the compound which is most reactive toward electrophilic aromatic substitution (EAS). Write "least" under the compound which is least reactive toward that EAS. NHC
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- Need help with Part 2: select all the appropriate resonance structures that result from the first step that is reproduced below.On the square, indicate the number of sites of unsaturation of the following molecules, show your work with one of the structures by applying the appropriate formula and showing the number (which should match the number on the square).OChem help with the following reaction schemes (see attached image) Please provide the bond line structures for the products obtained in the following reaction schemes... Notice in question #1 that A, B, and C are actually shown as C, B, and finally A in the actual reaction scheme so C correlates with PCC, and so on Question #2 is in order.
- By which substitution mechanism (SN1 or SN2) did the reaction occur? How did you know? For what reason does the substitution occur at only one of the bromine atoms, and in particular the bromine atom that it did?What is the correct answer here? Answer key says D but it doesn't make sense to me because the final one (5) is tertiary allylic.organic chemistry 1 Provide an overall order of carbocation stability, including every type of carbocations. (Not just primary< secondary<tertiary!) please help me this question, thank you!
- Please explain question 1 and 8 1. How many degrees of unsaturation are present in your unknown monosubstituted benzene starting material? 8. Based on all of the data provided, what is the identity of the “G” group? (Please NEATLY & CLEARLY draw its full Lewis structure in the space provided) Thank you!For each of the following, write the major product(s) and then draw out each step in the mechanism using curved arrows. Show ALL lone pair electrons and formal charges. Redraw ALL molecules as to show explicitly ALL bonds being broken or formed. Identify the molecular orbital (HOMO) of the nucleophile and the molecular orbital (LUMO) of electrophile involved in the nucleophilic attack. MO diagrams are not necessary..Kepone, aldrin, and chlordane are synthesized from hexachlorocyclopentadiene and other five-membered-ring compounds. Show how these three pesticides are composed of two five-membered rings.