Amines
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Aniline in a set of reactions yielded a product (D)
the structure of the product D would be
Aniline in a set of reactions yielded a product (D)
the structure of the product D would be
Aniline in a set of reactions yielded a product (D)
the structure of the product D would be
Aniline in a set of reactions yielded a product (D)
the structure of the product D would be
Statement-I: In aniline, –NH2 group is strong deactivating group for all ESR.
Statement-II: Aniline does not show Friedel-Craft alkylation reaction.
(1) Both statement-l and statement-II are correct
(2) Both statement-l and statement-II are incorrect
(3) Statement-l is correct and statement-II is incorrect
(4) Statement-l is incorrect and statement-Il is correct
Statement-I: In aniline, –NH2 group is strong deactivating group for all ESR.
Statement-II: Aniline does not show Friedel-Craft alkylation reaction.
(1) Both statement-l and statement-II are correct
(2) Both statement-l and statement-II are incorrect
(3) Statement-l is correct and statement-II is incorrect
(4) Statement-l is incorrect and statement-Il is correct
In aniline –NH2 is strong activating group due to presence of lone pair in nitrogen.
Aniline does not show Friedel-Craft alkylation reaction, because anhydrous AlCl3 and aniline form salt together
Upvote 
Consider the following reaction.
Select P
(Where Me is CH3)
Consider the following reaction.
Select P
(Where Me is CH3)
Upvote Statement-I : Aniline on reaction with concentrated H2SO4 at 475 K gives p-amino benzene sulphonic acid. This gives blood red colour with Lassaigne’s test.
Statement-II : Aniline forms a salt with anhydrous AlCl3 in Friedel Craft’s reaction.
Statement-I : Aniline on reaction with concentrated H2SO4 at 475 K gives p-amino benzene sulphonic acid. This gives blood red colour with Lassaigne’s test.
Statement-II : Aniline forms a salt with anhydrous AlCl3 in Friedel Craft’s reaction.
p-amino benzene sulphonic acid contains both N and S, so it gives blood red colour with Lassaigne's test.
Upvote What will be the reactivity order of following compounds towards electrophilic substitution reaction?
What will be the reactivity order of following compounds towards electrophilic substitution reaction?
Consider the following reaction
A and B respectively are
Consider the following reaction
A and B respectively are
The decreasing order of basic strength of the following is
The decreasing order of basic strength of the following is
Stronger the acid, weaker will be its Bronsted base.
Order of acidic strength:
Upvote The amine which is most basic in aqueous solution is
The amine which is most basic in aqueous solution is
Correct order of basic strength in aqueous medium is
(CH3)2NH > CH3NH2 > (CH3)3N > NH3
Upvote