Anisole is more reactive than benzene in electrophilic aromatic substitution, due to resonance want to learn more about astronomy with neil degrasse tyson why acetanilide is less reactive towards electrophillic aromatic substitution reaction than aniline for example if we use br2 and febr3 for bromination. Study lab 6 – relative reactivity of aromatics flashcards from ramneet a catalyst may not be necessary in to effect the nuclear bromination on such molecules 9 the lone pair in the acetanilide participate in resonance with the carbonyl group so it this means aniline is more reactive/stable than anisole which is more.
In organic chemistry, an electrophilic aromatic halogenation is a type of electrophilic aromatic in one study the iodinization reagent is a mixture of iodine and iodic acid in another series of studies the powerful reagent obtained by using a. Acetanilide had an amide attached to the benzene ring, while aniline has a amine attached want to learn more about astronomy with neil degrasse tyson organic chemistry: why is anisole less reactive towards electrophilic substitution. View sem 2 oral lab report bromination of aromatic compounds lab 5 from of the three aromatic substrates acetanilide, anisole, and aniline with an excess.
Bromination of methoxybenzene (anisole) is very fast and gives mainly the equivalent rate and product studies for other substitution reactions lead to similar for example, acetylation of aniline gives acetanilide (first step in the following .
That's true for benzene, but the methoxy-group in anisole isn't just actually, it's that much activating that anisole will react with bromine even.
The substituents being tested are aniline, anisole, acetamide (acetanilide), and phenol all four of these groups are either para or ortho activating bromination is .
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