Predict the product of reaction of aniline with bromine in non-polar solvent such as CS2.
In non-polar solvent (such as CS2) the activating effect of -NH2 group is reduced (due to resonance) and hence, mono substitution occurs only at o- and p-positions.
Under which of the following reaction conditions, aniline gives p-nitro derivative as the major product?
(a) Acetyl chloride/pyridine followed by reaction with cone. H2SO4 + cone.
(b) Acetic anhydride/pyridine followed by cone. H2SO4 + cone. HNO3
(c) Dil. HCl followed by reaction with cone. H2SO4 + cone. HNO3
(d) Reaction with cone. HNO3 + cone. H2S04
Which of the following reactions belong to electrophilic aromatic substitution?
(a) Bromination of acetanilide
(b) Coupling reaction of aryldiazonium salts
(c) Diazotisation of aniline
(d) Acylation of aniline
Assertion (A): N, N-diethylbenzene sulphonamide is insoluble in alkalf. Reason (R): Sulphonyl group attached to nitrogen atom is strong electron withdrawing group.
Describe a method for the identification of primary, secondary and tertiary amines. Also write chemical equations of the reactions involved.
Write following conversions:
(i) nitrobenzene –> acetanilide
(ii) acetanilide –> p-nitroaniline
Write IUPAC names of the following compounds and classify them into primary, secondary and tertiary amines.
(i) (CH3)2 CHNH2 (ii) CH3(CH2)2NH2 (iii) CH3NHCH(CH3)2
(iv) (CH3)3 CNH2 (v) C6H5NHCH3(vi) (CH3CH2)2NCH3
(vii)m-BrC6H4NH2
In the following questions, a statement of Assertion (A) followed by a statement of Reason (R) is given. Choose the correct answer out of the following choices:
(a) Both Assertion and Reason are wrong.
(b) Both Assertion and Reason are correct but Reason is not the correct explanation of Assertion.
(c) Assertion is correct but Reason is wrong.
(d) Both Assertion and Reason are correct and Reason is the correct explanation of Assertion.
(e) Assertion is wrong but Reason is correct.
Assertion (A): Acylation of amines gives a monosubstituted product, whereas alkylation of amines gives polysubstituted product.
Reason (R): Acyl group sterically hinders the approach of further acyl groups.
Why is benzene diazonium chloride not stored and is used immediately after its preparation?
Which of the following is a 3 ° amine?
(a) 1 -Methylcyclohexylamine (c) tert-Butylamine
Arrange the following in increasing order of their basic strength: ‘
(i) C2H5NH2,C6H5NH2,NH3,C6H5CH2NH2 and(C2H5)2 NH
(ii) C2H5NH2,(C2H5)2NH,(C2H5)3N,C6H5NH2
(iii) CH3NH2, (CH3)2NH, (CH3)3N, C6H5NH2, C6H5CH2NH2
Assertion (A): Hofmann's bromamide reaction is given by primary amines. Reason (R): Primary amines are more basic than secondary amines.
The correct IUPAC name for CH2 = CHCH2NHCH3 is
(a) allylmethylamine (b) 2-amino-4-pentene
(c) 4-aminopent-l-ene . (d) N-methylprop-2-en-l-amine.
Write reactions of the final alkylation product of aniline with excess of methyl iodide in the presence of sodium carbonate solution.
The reagents that can be used to convert benzene diazonium chloride to benzene are
(a) SnCl2/HCl (b) CH3CH2OH
(c) H3PO2 (d) LiAlH4
Which of the following amines can be prepared by Gabriel synthesis?
(a) Isobutyl amine (b) 2-Phenylethylamine
(c) N-Methylbenzylamine (d) Aniline
Assertion (A): Only a small amount of HCl is required in the reduction of nitro compounds with iron scrap and HCl in the presence of steam.
Reason (R): FeCl2 formed gets hydrolysed to release HCl during the reaction.
Assertion (A): Acetanilide is less basic than aniline.
Reason (R): Acetylation of aniline results in decrease of electron density on nitrogen.
Write chemical reaction of aniline with benzoyl chloride and write the name of the product obtained.
A compound Z with molecular formula C3H9N reacts with C6H5SO2Cl to give a solid, insoluble in alkali, identify Z.
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.
The best reagent for converting 2-phenylpro-panamide into-2-phenyl- propanamine is .
(a) excess H2
(b) Br2 in aqueous NaOH
(c) iodine in the presence of red phosphorus
(d) LiAlH4 in ether
Account for the following
(i)pKb of aniline is more than that of methylamine
(ii) Ethylamine is soluble in water whereas aniline is not.
(iii) Methylamine in water reacts with ferric chloride to precipitate hydrated ferric oxide.
(iv)Although amino group is o and p – directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of m-nitroaniline.
(v)Aniline does not undergo Friedel-Crafts reaction.
(vi)Diazonium salts of aromatic amines are more stable than those of aliphatic amines.
(vii)Gabriel phthalimide synthesis is preferred for synthesising primary amines.
An aromatic compound 'A'on treatment with aqueous ammonia and heating forms compound 'B' which on heating with Br2 and KOH forms a compound 'C' of molecular formula C6H7N. Write the structures and IUPAC names of compounds A,B and C.
Give plausible explanation for each of the following:
(i) Why are amines less acidic than alcohols of comparable molecular masses?
(ii) Why do primary amines have higher boiling point than tertiary amines?
(iii) Why are aliphatic amines stronger bases than aromatic amines?
