In Aromatic Electrophilic Substitution reaction, a cationic sigma complex form as an intermediate. Now the reaction rate will be faster for that molecule only which stabilize the intermediate sigma complex more.
Among the compounds, compound 3(para methoxy toluine) will be most reactive because lone pair present in the oxygen atom take participate in the resonance and hence will show most reactivity.
Which of the following molecules is the most reactive towards electrophilic aromatic substitution (EAS)? (all EDG...
Given the following molecules, answer the following questions. 5. Given the following molecules, answer the given questions: CH3 OMe TOMe 0 OМен NO2 NO₂ H₃c OMe ON NO, H3C А a. Which structure is the most reactive towards any electrophilic aromatic substitution? B b. Which structure is the least reactive towards any electrophilic aromatic substitution? c. Which structure has both EWG and EDG moieties?'
5. Given the following molecules, answer the given questions: CH3 TecDE OMe I cot T bernable hyde 1, 3m y toluene H₂c NO2 a WG OME EDO ON NO Beve Quoc cho a. Which structure is the most reactive towards any electrophilic aromatic substitution? b. Which structure is the least reactive towards any electrophilic aromatic substitution? c. Which structure has both EWG and EDG moieties?' A
In the following compound, select the position that is most reactive towards electrophilic aromatic substitution reaction. Review of Skills - Skill Builder 18.03 X Incorrect. Tert-butyl (activator) will direct the incoming electrophile and it is an ortho-para director. In the following compound, select the position that is most reactive towards electrophilic aromatic substitution reaction. NO,
,,,,,,,,,,, Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution. Most reactive Least reactive COOH H3C CH3 COOH HaC
Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution Most reactive Least reactive COOH H3C CH3 HOOC- COOH
3. The electrophilic aromatic substitution (EAS) reaction is a great way to prepare substitute Provide the expected major product for each of the following EAS reactions. (12 pts) SO3H HNO3 H2SO4 CH2CH3 CI AICI en Enhen II Ph-C-NHÓh Br2 CH3 -CH₃ CH3 FeBr3
Which of the following compounds is the most reactive toward electrophilic aromatic substitution? IV H III IT IN
organic chemistry 353 2. (4 pts.) Arrange the following in order of increasing electrophilic aromatic substitution reactivity (4 = most reactive): SO3H OH e 3. (4 pts.) Briefly describe why alkenes undergo addition and aromatic compounds undergo substitution. n Briefly describe w 4. (5 pts. Provide an example of an EAS reaction creates an arene that is less reactive than benzene (be specific, include reagents, you do not need to show the mechanism)
Which benzene derivative would be the most reactive in an electrophilic aromatic substitution reaction? O A. ON B. Br OC. OD.
Which benzene derivative would be the most reactive in an electrophilic aromatic substitution reaction? )A OB ON BT D Which is the most stable radical? O A. B. C. D.