9. Rank the compounds below in order of reactivity to Electrophilic Aromatic Substitution. Rank the most reactive compound as compound 1 and the least reactive compound as compound 5. OH NO2 CH SO3H
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- 4. Identify the position where electrophilic aromatic substitution is most favorable. * HN CH3 CH3 A B O A O A and CConsider the following arormatic.compounds N(CHh N(CH3)2 NH2 OCH, NON, NO NO2 OCH ARO MAT TIC HYD ROC a meto-substtuted compound Choose S the most reactive towards EAS the least reactive towards EAS Choose an ortho-substituted compoundRank the compounds by DECREASING reactivity towards nitration with HNO3/ H2SO4 (most reactive on the left). NO2 CH3 II III IV O A. V>V>I> || > || O B. V>I> III > || > IV oCV> || >1> V> I| O D. I > V> > || > IV O E. II > V >1> [IV >| Moving to another question will save this response. Co search
- ت ا كل وخویه م اکتریار Q6/ Rank the compounds in each group in order of increasing reactivity in electrophilic aromatic substitution. NH NO2 b) O O D4. The purine heterocycle occurs commonly in the structure of DNA. a. How is each N atom hybridized? b. In what type of orbital does each lone pair on a N atom reside? c. How manyn electrons does purine contain? d. Why is purine aromatic? :N H. purine batond ai enexerlo 08,H HO HO HO b w bemmot etbubong erit wea OH8 HOH2O zhemala eriT nertw bemotRank the following structures in order of decreasing electrophile strength. most electrophilic least electrophilic CF3 `CF3 Н
- organic chemistry help with carboxylic acids Rank the following from most reactive (left) to least reactive (right) with potassium ethoxide.These are all electron-withdrawing groups that slow electrophilic aromatic substitution, with one exception. Which one? © CO,H O NO₂ O CF3 O NH2Cyclopentadiene is unusually acidic for a hydrocarbon. Which of the following explains why that is? The carbon atoms of cyclopentadiene are all sp hybridized. A В Cyclopentadiene is aromatic. Removal of a proton from cyclopentadiene yields an C aromatic anion. Removal of a hydrogen atom from cyclopentadiene yields a highly stable free radical. D Removal of a hydride ion from cyclopentadiene produces an E aromatic cation. H H. cyclopentadiene
- Rank the following according to INCREASING reactivity towards SN2: 1st (least reactive)? 2ND? 3RD? 4TH (most reactive)?What is the correct order of decreasing reactivity (most reactive first) of these compounds toward electrophilic aromatic substitution? CH3 a) | > | > | c) || > | > III OCH3 18 b) III > II >I d) II > III > I LOCH3Arrange the following according to INCREASING reactivity towards E2: 1st ( least reactive)? 2nd? 3rd? 4th (most reactive)?