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Answer 1,2,3,4 please thank you!Aniline is very readily brominated in aqueous conditions at room temperature in comparison to benzene (high temperature and F

-NH2 is one of the most powerful ortho/para activators in electrophilic aromatic substitution. However, attempts to nitrate a

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1 Lel s conoiden anilme the anikine ha Nitnegen atom cahich contain lone pain So, it can daice pt H and act as an Lewis baneH NH The both cmkaund al show 1z effect and act as an achvaton. but n B THe one-pain is in congugaion aith the =0ghoup so avaNH2 Reno onating stnchuner 1 the tR esfect of the (-N)ano Activated sthongy in the thenyA ning So such +R) effect is found in

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  • -NH2 is one of the most powerful ortho/para activators in electrophilic aromatic substitution. However, attempts to nit...

    -NH2 is one of the most powerful ortho/para activators in electrophilic aromatic substitution. However, attempts to nitrate aniline under standard conditions leads to the formation of m-nitroaniline (3%) with 97% of aniline remaining unchanged. Why is this? Hint: -NH2 is a base as well as an activator. 3. Why are amines more activating than amides? NH2 Aniline is very readily brominated in aqueous conditions at room temperature in comparison to benzene (high temperature and FeBr3 catalysis is required). When aniline...

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