CBSE
Which of the following reactions is appropriate for converting acetamide to methanamine?
Carbylamine reaction
Hoffmann hypobromamide reaction
Stephens reaction
Stephens reaction
The correct order of N-compounds in its decreasing order of oxidation states is
HNO3, NH4Cl, NO, N2
HNO3, NO,NH4Cl, N2
HNO3, NO, N2, NH4Cl
NH4Cl, N2, NO, HNO3
Nitration of aniline in strong acidic medium also gives m-nitroaniline because
Inspite of substituents nitro group always goes to only m-position.
In electrophilic substitution reactions amino group is meta directive.
In acidic (strong) medium aniline is present as anilinium ion.
In absence of substituents nitro group always goes to m-position.
Which of the following carbocations is expected to be most stable?
In a reaction of aniline, a coloured product C was obtained.
Which of the following is more basic than aniline?
Diphenylamine
Triphenylamine
p-nitroaniline
p-nitroaniline
The correct increasing order of basic strength for the following compounds is
II < III < I
III < I < II
III < II < I
III < II < I
Predict the product,
Which one of the following on reduction with lithium aluminium hydride yield a secondary amine?
Nitroethane
Methylisocyanide
Acetamide
Acetamide
Which of the following compounds can form a zwitter ion?
Aniline
Acetanilide
Glycine
Benzoic acid