In the following compound, select the position that is most
reactive towards electrophilic aromatic substitution
reaction.
Answer:-
C4 is the correct answer
because C4 is the para position of alkyl group and meta position for nitro group.
In the following compound, select the position that is most reactive towards electrophilic aromatic substitution reaction....
Write the mechanism for an electrophilic aromatic substitution reaction given any aromatic compound and either chlorine, Cl2, or t-butyl cation as the electrophile
Which of the following molecules is the most reactive towards electrophilic aromatic substitution (EAS)? (all EDG on the benzene) Н. CH3 CN SO3H NO2 OME 1 II IV
,,,,,,,,,,, Rank the compounds below in order of decreasing reactivity towards electrophilic aromatic substitution. Most reactive Least reactive COOH H3C CH3 COOH HaC
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6. (9 pts) In regards to an electrophilic aromatic substitution reaction, define the 3 compounds shown below as either: a) Activating, ortho, para director b) Deactivating, ortho para director, c) Activating, meta director, d) Deactivating, meta director. CH -ОН -N-CH3 CH3 7. Answer a-c for compounds A-F below dos a. (5 pts) Which compound(s) have an aromatic carbocation intermediate if it underwent an Snl or E1 reaction? b. (5 pts) Which compound(s) would have an anti-aromatic carbocation intermediate if it...
Please help... Need a detail Mechanism of this reaction. Thanks... Electrophilic aromatic substitution describes the reaction where a hydrogen from a benzene ring is replaced by an electrophile. Halogenation, nitration, sulfonation, alkylation and acylation are all possible using this type of reaction. The electrophile attacks the pi electrons of the aromatic ring, yielding a benzenonium ion. The substituted aromatic product is obtained when a proton is lost, restoring the aromatic system. If there is a substituent on the aromatic ring...
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