Which of the following is a 3° amine?
- (i)1-methylcyclohexylamine
- (ii)Triethylamine
- (iii)tert-butylamine
- (iv)N-methylaniline
Show answer
(ii) Triethylamine
Class 12 Chemistry · 67 questions · 61 with answers
Which of the following is a 3° amine?
(ii) Triethylamine
The correct IUPAC name for CH2==CHCH2 NHCH3 is
(iv) N-methylprop-2-en-1-amine
Amongst the following, the strongest base in aqueous medium is ____________.
(iii) (CH3)2 NH
Which of the following is the weakest Brönsted base?
(i)
Benzylamine may be alkylated as shown in the following equation : C6H5CH2NH2 + R—X → C6H5CH2NHR Which of the following alkylhalides is best suited for this reaction through SN1 mechanism?
(iii) C6H5CH2Br
Which of the following reagents would not be a good choice for reducing an aryl nitro compound to an amine?
(ii) LiAlH4 in ether
In order to prepare a 1° amine from an alkyl halide with simultaneous addition of one CH2 group in the carbon chain, the reagent used as source of nitrogen is ___________.
(iii) Potassium cyanide, KCN – +
The source of nitrogen in Gabriel synthesis of amines is _____________.
(iv) Potassium phthalimide, C6H4(CO)2N K
Amongst the given set of reactants, the most appropriate for preparing 2° amine is _____.
(iii) 1° R—NH2 + RCHO followed by H2/Pt
The best reagent for converting 2–phenylpropanamide into 2-phenylpropanamine is _____.
(iv) LiAlH4 in ether
The best reagent for converting, 2-phenylpropanamide into 1- phenylethanamine is ____.
(ii) NaOH/Br2
Hoffmann Bromamide Degradation reaction is shown by __________.
(ii) ArCONH2
The correct increasing order of basic strength for the following compounds is _________. (I) (II) (III)
(iv) II < I < III
Methylamine reacts with HNO2 to form _________.
(iii) CH3OH
The gas evolved when methylamine reacts with nitrous acid is __________.
(ii) N2
In the nitration of benzene using a mixture of conc. H2SO4 and conc. HNO3, the species which initiates the reaction is __________.
(iii) NO2 –
Reduction of aromatic nitro compounds using Fe and HCl gives __________.
(iii) aromatic primary amine
The most reactive amine towards dilute hydrochloric acid is ___________.
(ii)
Acid anhydrides on reaction with primary amines give ____________.
(i) amide
The reaction Ar N2Cl → ArCl + N2 + CuCl is named as _________.
(ii) Gatterman reaction
Best method for preparing primary amines from alkyl halides without changing the number of carbon atoms in the chain is
(ii) Gabriel phthalimide synthesis
Which of the following compound will not undergo azo coupling reaction with benzene diazonium chloride.
(iv) Nitrobenzene
Which of the following compounds is the weakest Brönsted base?
(iii)
Among the following amines, the strongest Brönsted base is __________.
(iv)
The correct decreasing order of basic strength of the following species is _______. – – H2O, NH3, OH , NH2 – –
(i) NH2 > OH > NH3 > H2O – –
Which of the following should be most volatile? (I) CH3CH2CH2NH2 (II) (CH3)3N (III) (IV) CH3CH2CH3
(ii) IV
Which of the following methods of preparation of amines will give same number of carbon atoms in the chain of amines as in the reactant?
(iii) Heating alkylhalide with potassium salt of phthalimide followed by hydrolysis.
Which of the following cannot be prepared by Sandmeyer’s reaction?
(iii) Iodobenzene
(iv) Fluorobenzene
Reduction of nitrobenzene by which of the following reagent gives aniline?
(i) Sn/HCl
(ii) Fe/HCl
(iii) H2-Pd
Which of the following species are involved in the carbylamine test?
(i) R—NC
(ii) CHCl3
The reagents that can be used to convert benzenediazonium chloride to benzene are __________.
(ii) CH3CH2OH
(iii) H3PO2
The product of the following reaction is __________.
(i)
(ii)
Arenium ion involved in the bromination of aniline is __________.
(i)
(ii)
(iii)
Which of the following amines can be prepared by Gabriel synthesis.
(i) Isobutyl amine
(ii) 2-Phenylethylamine
Which of the following reactions are correct?
(i)
(iii)
Under which of the following reaction conditions, aniline gives p-nitro derivative as the major product?
(i) Acetyl chloride/pyridine followed by reaction with conc. H2SO4 + conc. HNO3.
(ii) Acetic anyhdride/pyridine followed by conc. H2SO4 + conc. HNO3.
Which of the following reactions belong to electrophilic aromatic substitution?
(i) Bromination of acetanilide
(ii) Coupling reaction of aryldiazonium salts
What is the role of HNO3 in the nitrating mixture used for nitration of benzene?
HNO3 acts as a base in the nitrating mixture and provides the electrophile, + NO2 .
Why is NH2 group of aniline acetylated before carrying out nitration?
See NCERT textbook for Class XII.
What is the product when C6H5CH2NH2 reacts with HNO2?
C6H5CH2OH
What is the best reagent to convert nitrile to primary amine?
Reduction of nitriles with sodium/alcohol or LiAlH4 gives primary amine.
Give the structure of ‘A’ in the following reaction.
What is Hinsberg reagent?
Benzene sulphonylchloride.
Why is benzene diazonium chloride not stored and is used immediately after its preparation?
Benzene diazonium chloride is very unstable.
Why does acetylation of —NH2 group of aniline reduce its activating effect?
See NCERT textbook for Class XII.
Explain why MeNH2 is stronger base than MeOH?
Nitrogen is less electronegative than oxygen therefore lone pair of electrons on nitrogen is readily available for donation. Hence, MeNH2 is more basic than MeOH.
What is the role of pyridine in the acylation reaction of amines?
Pyridine and other bases are used to remove the side product i.e. HCl from the reaction mixture.
Under what reaction conditions (acidic/basic), the coupling reaction of aryldiazonium chloride with aniline is carried out?
Reaction is done in mild basic conditions.
Predict the product of reaction of aniline with bromine in non-polar solvent such as CS2.
A mixture of 2-bromoaniline and 4-bromoaniline is formed. (2-Bromoaniline) (4-Bromoaniline)
Arrange the following compounds in increasing order of dipole moment. CH3CH2CH3, CH3CH2NH2, CH3CH2OH
CH3CH2CH3 < CH3CH2NH2 < CH3CH2OH
What is the structure and IUPAC name of the compound, allyl amine?
CH2== CH—CH2—NH2, prop-2-en-1-amine
Write down the IUPAC name of
N, N-Dimethylbenzenamine
A compound Z with molecular formula C3H9N reacts with C6H5SO2Cl to give a solid, insoluble in alkali. Identify Z.
Z is an aliphatic amine which gives a solid insoluble in base. This implies that reaction with C6H5SO2Cl must give a product without any replaceable hydrogen attached to nitrogen. In other words, the amine must be a secondary amine. i.e. Z is ethylmethylamine.
A primary amine, RNH2 can be reacted with CH3—X to get secondary amine, R—NHCH3 but the only disadvantage is that 3° amine and quaternary ammonium salts are also obtained as side products. Can you suggest a method where RNH2 forms only 2° amine?
Carbylamine reaction is shown by 1° amine only which results in the replacement of two hydrogen atoms attached to nitrogen atom of NH2 group by one carbon atom. On catalytic reduction the isocyanide will give a secondary amine with one methyl group.
Complete the following reaction. 189 Amines
The reaction exhibits azo-coupling of phenols. In mild alkaline conditions phenol moiety participates in the azo-coupling and para position of phenol is occupied. 195 Amines
Why is aniline soluble in aqueous HCl?
Aniline forms the salt anilinium chloride which is water soluble.
Suggest a route by which the following conversion can be accomplished.
Identify A and B in the following reaction.
How will you carry out the following conversions?
(i) toluene → p-toluidine
(ii) p-toluidine diazonium chloride → p-toluic acid
Write following conversions:
(i) nitrobenzene → acetanilide
(ii) acetanilide → p-nitroaniline
A solution contains 1 g mol. each of p-toluene diazonium chloride and p- nitrophenyl diazonium chloride. To this 1 g mol. of alkaline solution of phenol is added. Predict the major product. Explain your answer.
This reaction is an example of electrophilic aromatic substitution. In alkaline medium, phenol generates phenoxide ion which is more electron rich than phenol and hence more reactive for electrophilic attack. The electrophile in this reaction is aryldiazonium cation. Stronger the electrophile faster is the reaction. p-Nitrophenyldiazonium cation is a stronger electrophile than p-toluene diazonium cation. Therefore, it couples preferentially with phenol. 197 Amines
How will you bring out the following conversion?
How will you carry out the following conversion? NO2 → NH2
How will you carry out the following conversion? NH2 NO2 →
How will you carry out the following conversions?
(i)
(ii)
Match the reactions given in Column I with the statements given in Column II. Column I Column II (i) Ammonolysis
(a) Amine with lesser number of carbon atoms (ii) Gabriel phthalimide synthesis
(d) Reaction of alkylhalides with NH3
(b) Detection test for primary amines. (iii) Hoffmann Bromamide reaction
(c) Reaction of phthalimide with KOH and R—X (iv) Carbylamine reaction
Match the compounds given in Column I with the items given in Column II. Column I Column II (i) Benzene sulphonyl chloride
(a) Zwitter ion (ii) Sulphanilic acid
(b) Hinsberg reagent (iii) Alkyl diazonium salts
(c) Dyes (iv) Aryl diazonium salts
(d) Conversion to alcohols 191 Amines