Mark the correct statement 
Methyl amine is a stronger base than
ammonia due to +I effect. The alkyl groups
which are electron releasing groups increase
the electron density around the nitrogen
thereby increasing the availability of the lone
pair of electrons to proton or lewis acid and
making the amine more basic
Indicate which nitrogen compound amongst thefollowing would undergo Hofmann reaction (i.e..,reaction with Br2 and strong KOH) to furnish theprimary amine (R – NH2) 
Only 1° amides (i.e. RCONH2) in the present case undergo Hoffmann bromamide reaction.
(Hoffman's bromamide reaction)
For carbylamine reaction, we need hot alcoholic KOH and 
Any primary amine means both aliphatic as well as aromatic but onoalkylamines means only 1° aliphatic amines. Therefore, option (a) is correct while (d) is wrong.
What is the decreasing order of basicity of primary, secondary and tertiary ethylamines and NH3 ? 
In the solution phase, amines follow the reactivity as 2°>3°>1°>NH3, provided the alkyl group is not methyl.
Acetamide and ethylamine can be distinguishedby reacting with 
Acetamide and ethylamine can be
distinguished by heating with NaOH
solution. Acetamide evolves NH3 but
ethylamine does not.
Which is formed, when acetonitrile is hydrolysedpartially with cold concentrated HCl? 
Methyl cyanide on treatment with conc. HCl give acetamide.
When aniline reacts with oil of bitter almonds(C6H5CHO) condensation takes place andbenzal derivative is formed. This is known as 
Benzaldehyde reacts with primary aromatic amine to form schiff's base
This is know as Schiff’s base reaction.
Consider the following sequence of reactions :
The compound [A] is 
Aniline is an activated system for electrophilic substitution. The compound formed on heating aniline with acetic anhydride is 
Aniline when treated with acetic anhydride forms acetanilide (nucleophilic substitution)
The compound obtained by heating a mixture ofa primary amine and chloroform with ethanolicpotassium hydroxide (KOH) is 
In this reaction, bad smelling compound ethyl isocyanide (CH3CH2NC) is produced. This equation is known as carbyl amine reaction.
Aniline is reacted with bromine water and theresulting product is treated with an aqueoussolution of sodium nitrite in presence of dilutehydrochloric acid. The compound so formed isconverted into a tetrafluoroborate which issubsequently heated dry. The final product is 
An isocyanide is prepared by 
Carbylamine reaction :
Which of the following reagents will convert pmethylbenzenediazoniumchloride into p-cresol? 
The consituent of the powerful explosive RDX is formed during the nitration of 
RDX is prepared by treating urotropine with fuming nitric acid. When the inner bridge system is destroyed by oxidation and the peripheral nitrogen atom are nitrated, it forms cyclonitrite (or RDX).
Which of the following is most basic in nature? 
(CH3)2NH is most basic because two electron releasing groups are present on Nitrogen. Also aromatic amines are less basic then aliphatic amines. The basic character of amines follow
R2NH > RNH2 > C6H5NHCH3 > NH3
Intermediates formed during reaction of with Br2 and KOH are 
The mecahnism of Hoffmann bromide
RCONH2 + Br2 →RCONHBr + HBr
Product 'P' in the above reaction is 
The final product C, obtained in this reaction
Aniline when diazotized in cold and when treated with dimethyl aniline gives a coloured product. Its structure would be 
Aniline in a set of reactions yielded a product D.
The structure of the product D would be: 
The major organic product formed from the following reaction :
Electrolytic reduction of nitrobenzene in weaklyacidic medium gives 
Electrolytic reduction of Nitroalkane in
weakly acidic medium give aniline
Whereas in strongly acidic medium it gives p-hydroxyaniline
Which of the following is more basic thananiline? 
Benzylamine is more basic than aniline. The reason is that in aniline, the lone pair of nitrogen is conjugated with benzene ring so it is not available readily for others. On the other hand in Benzylamine, nitrogen is not directly attached with ring so lone pairs are
not conjugated with ring.
Which one of the following on reduction withlithium aluminium hydride yields a secondaryamine? 
Reduction of alkyl isocyanides in presence of LiAlH4 yields secondary amines containing methyl as one of the alkyl group.
whereas, alkyl cyanides give 1° amine on reduction.
In a reaction of aniline a coloured product C was obtained. 
The structure of C would be :
The reaction can be completed as follows:
Predict the product: 
Secondary amine with (NaNO2 + HCl) gives nitroso product
Nitrobenzene can be prepared from benzene byusing a mixture of conc. HNO3 and conc. H2SO4 in the mixture, nitric acid acts as a/an: 
Nitric acid acts as a base by accepting a proton.
Aniline in a set of the following reactions yielded a coloured product ‘Y’ 
The structure of ‘Y’ would be ;
Acetamide is treated with the following reagentsseparately. Which one of these would yieldmethylamine? 
Which of the following statements about primaryamines is ‘False’ ? 
Aryl amines do not produce phenol on
treatment with nitrous acid
Match the compounds given in List - I with their characteristic reactions given in List - II. Select the correct option. 
(1) CH3 CH2 – CH2 – CH2 – NH2
(ii) with KOH (alcohol) and CHCl3
produces bad smell
(2) CH3C ≡ CH
(ii) gives white ppt with ammonical
(3) CH3 CH2 COOCH3
(i) alkaline hydrolysis
(4) CH3 CHOH – CH3
(iv) with Lucas reagent cloudiness
appears after 5 minutes
In a set of reactions m-bromobenzoic acid gave a product D. Identify the product D. 
What is the product obtained in the following reaction : 
When nitro compound is reduced with a
neutral reducing agent (Zn dust + NH4Cl) the corresponding hydroxyl amine is formed
Which of the following compounds is most basic? [2011 M]
compound is most basic due to localized lone pair of electron on nitrogen atom while other compounds have delocalized lone pair of electron.
An organic compound (C3H9N) (A), when treated with nitrous acid, gave an alcohol and N2 gas was evolved. (A) on warming with CHCl3 and caustic potash gave (C) which on reduction gave isopropylmethylamine. Predict the structure of (A). [2012 M]
In the reaction
A is : [NEET 2013]
Nitrobenzene on reaction with conc. HNO3/H2SO4 at 80 - 100°C forms which one of thefollowing products ? [NEET 2013]
On hydrolysis of a “compound”, twocompounds are obtained. One of which ontreatment with sodium nitrite and hydrochloricacid gives a product which does not respond toiodoform test. The second one reduces Tollen’sreagent and Fehling’s solution. The “compound”is [NEET Kar. 2013]
Hydrolysis gives CH3CH2CH2NH2 +
HCOOH. On treatment with NaNO2 and
HCl former gives CH3CH2CH2OH which
does not give iodoform test. HCOOH gives Tollen’s reagent test.
Some reactions of amines are given. Which one is not correct ? [NEET Kar. 2013]
Secondary amine react with nitrous acid to give N-Nitrosoamines.