Practice MCQs for JEE Chemistry Amines
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Multiple Choice Questions
(a) nucleophilic
(b) electrophilic
(c) strongly acidic
(d) non-reactive and neutral
Show Answer & Explanation
Answer: (a) nucleophilic
Explanation:
1. CN- has a lone pair on carbon and attacks electron-poor centres, so it is a nucleophile.
Teacher's Note:
1. Always link acid strength to the stability of the carboxylate ion.
2. Electron-withdrawing groups increase acidity and electron-donating groups decrease it.
(a) diamines
(b) unknown
(c) amino acids
(d) enzymes
Show Answer & Explanation
Answer: (c) amino acids
Explanation:
1. An amino acid carries an amino group and a carboxyl group, as in glycine H2NCH2COOH.
Teacher's Note:
1. Note the name reaction and write its equation once in your notebook.
2. Such one-step recall questions are common in the JEE and NEET style papers.
(a) ethylenediamine
(b) dimethylamine
(c) trimethylamine
(d) N-methylaniline
Show Answer & Explanation
Answer: (a) ethylenediamine
Explanation:
1. In H2N-CH2CH2-NH2 each nitrogen is attached to one carbon, so both are primary amino groups.
2. The others are secondary or tertiary.
Teacher's Note:
1. Count carbons before and after the reaction to avoid mistakes in chain-length changes.
2. Check whether the reagent is a reducing, oxidising or dehydrating agent before choosing the product.
(a) a primary amine
(b) a secondary amine
(c) a tertiary amine
(d) all of these
Show Answer & Explanation
Answer: (d) all of these
Explanation:
1. Propylamine and isopropylamine are primary, ethylmethylamine is secondary and trimethylamine is tertiary, all with the formula C3H9N.
Teacher's Note:
1. Eliminate options by checking functional groups on both sides of the reaction.
2. Only one option will have the correct functional group and carbon skeleton.
(a) diacetone
(b) acetoneamine
(c) diacetoneamine
(d) aminoacetone
Show Answer & Explanation
Answer: (c) diacetoneamine
Explanation:
1. This 4-amino-4-methylpentan-2-one is obtained from acetone (two acetone units) and ammonia, and is called diacetoneamine.
Teacher's Note:
1. Revise the physical properties such as hydrogen bonding and boiling points together with the chemistry.
2. Compare similar compounds in pairs when you are asked to rank them.
(a) an organic compound with two -NH2 groups
(b) a compound with two carbon atoms and an -NH2 group
(c) a compound with an -NH2 group on carbon number 2
(d) a compound in which two of the hydrogens of NH3 have been replaced by organic groups
Show Answer & Explanation
Answer: (d) a compound in which two of the hydrogens of NH3 have been replaced by organic groups
Explanation:
1. Replacing one H of ammonia gives a primary amine, two H give a secondary amine and three H a tertiary amine.
Teacher's Note:
1. Learn the reactivity order of acid derivatives: acyl chloride, anhydride, ester, amide.
2. Most questions of this type are solved by recalling the standard reagent and product pair.
(a) (CH3)2CHNH2
(b) (CH3)3N
(c) (CH3)2NH
(d) CH3NH2
Show Answer & Explanation
Answer: (c) (CH3)2NH
Explanation:
1. Aminomethane is CH3NH2, and a methyl group on its nitrogen gives CH3NHCH3, dimethylamine.
Teacher's Note:
1. Always link acid strength to the stability of the carboxylate ion.
2. Electron-withdrawing groups increase acidity and electron-donating groups decrease it.
(a) 9 sigma bonds and 4 pi bonds
(b) 9 sigma bonds and 5 pi bonds
(c) 8 sigma bonds, 3 pi bonds and 4 non-bonding electrons
(d) 9 sigma bonds, 3 pi bonds and 2 non-bonding electrons
Show Answer & Explanation
Answer: (d) 9 sigma bonds, 3 pi bonds and 2 non-bonding electrons
Explanation:
1. Sigma bonds: 5 C-H, 2 C-C (including the sigma of C=C), 1 C-N and 1 N-C of the triple bond, a total of 9.
2. Pi bonds: 1 in C=C and 2 in N≡C, a total of 3.
3. The terminal carbon of the isocyanide carries one lone pair (2 electrons).
Teacher's Note:
1. Note the name reaction and write its equation once in your notebook.
2. Such one-step recall questions are common in the JEE and NEET style papers.
(a) secondary amine
(b) tertiary amine
(c) primary amine
(d) quaternary salt
Show Answer & Explanation
Answer: (c) primary amine
Explanation:
1. Each NH2 group is attached to a ring carbon and has two hydrogens, so the compound is a primary aromatic amine.
Teacher's Note:
1. Count carbons before and after the reaction to avoid mistakes in chain-length changes.
2. Check whether the reagent is a reducing, oxidising or dehydrating agent before choosing the product.
(a) secondary amine
(b) primary amine
(c) tertiary amine
(d) none of these
Show Answer & Explanation
Answer: (a) secondary amine
Explanation:
1. The nitrogen carries two carbon groups (allyl and methyl) and one hydrogen.
Teacher's Note:
1. Eliminate options by checking functional groups on both sides of the reaction.
2. Only one option will have the correct functional group and carbon skeleton.
(a) CH3-N=C=O
(b) CH3-C-N=S
(c) CHCl3
(d) C6H5COCl
Show Answer & Explanation
Answer: (a) CH3-N=C=O
Explanation:
1. Methyl isocyanate, CH3NCO, leaked from the storage tank.
Teacher's Note:
1. Revise the physical properties such as hydrogen bonding and boiling points together with the chemistry.
2. Compare similar compounds in pairs when you are asked to rank them.
(a) C6H5NO2
(b) CH3CH2ONO
(c) CH3CH(CH3)NO2
(d) C6H4(OH)NO2
Show Answer & Explanation
Answer: (b) CH3CH2ONO
Explanation:
1. A nitro compound has the carbon bonded to nitrogen, C-NO2.
2. CH3CH2ONO has C-O-N=O, so it is an alkyl nitrite.
Teacher's Note:
1. Learn the reactivity order of acid derivatives: acyl chloride, anhydride, ester, amide.
2. Most questions of this type are solved by recalling the standard reagent and product pair.
(a) C2H5CN
(b) CH3CN
(c) CH3COCN
(d) C6H5CH2CN
Show Answer & Explanation
Answer: (b) CH3CN
Explanation:
1. Acetonitrile (methyl cyanide) is CH3CN, the nitrile of acetic acid.
Teacher's Note:
1. Always link acid strength to the stability of the carboxylate ion.
2. Electron-withdrawing groups increase acidity and electron-donating groups decrease it.
(a) the C of the CN group
(b) the N of the CN group
(c) either C or N of the CN group
(d) both C and N of the CN group
Show Answer & Explanation
Answer: (a) the C of the CN group
Explanation:
1. In R-C≡N the alkyl group is bonded to carbon.
2. Attachment through nitrogen gives isocyanide, R-N≡C.
Teacher's Note:
1. Note the name reaction and write its equation once in your notebook.
2. Such one-step recall questions are common in the JEE and NEET style papers.
(a) 3
(b) 4
(c) 5
(d) 6
Show Answer & Explanation
Answer: (b) 4
Explanation:
1. Butan-1-amine, butan-2-amine, 2-methylpropan-1-amine and 2-methylpropan-2-amine.
Teacher's Note:
1. Count carbons before and after the reaction to avoid mistakes in chain-length changes.
2. Check whether the reagent is a reducing, oxidising or dehydrating agent before choosing the product.
(a) Perkin
(b) Hofmann
(c) Claisen
(d) Kolbe
Show Answer & Explanation
Answer: (b) Hofmann
Explanation:
1. The Hofmann bromamide (degradation) reaction converts an amide into a primary amine with one carbon fewer.
Teacher's Note:
1. Eliminate options by checking functional groups on both sides of the reaction.
2. Only one option will have the correct functional group and carbon skeleton.
(a) CH3Br
(b) CH4
(c) CH3COBr
(d) CH3NH2
Show Answer & Explanation
Answer: (d) CH3NH2
Explanation:
1. Hofmann degradation removes the carbonyl carbon, so acetamide gives methylamine.
Teacher's Note:
1. Revise the physical properties such as hydrogen bonding and boiling points together with the chemistry.
2. Compare similar compounds in pairs when you are asked to rank them.
(a) PCl5
(b) NaOH + Br2
(c) sodalime
(d) hot conc. H2SO4
Show Answer & Explanation
Answer: (b) NaOH + Br2
Explanation:
1. NaOH + Br2 (that is NaOBr) carries out Hofmann bromamide degradation to CH3NH2.
2. PCl5 gives CH3CN (via dehydration).
Teacher's Note:
1. Learn the reactivity order of acid derivatives: acyl chloride, anhydride, ester, amide.
2. Most questions of this type are solved by recalling the standard reagent and product pair.
(a) the same number of C atoms as that of amide
(b) one less C atom than that of amide
(c) one more C atom than that of amide
(d) two more C atoms than that of amide
Show Answer & Explanation
Answer: (b) one less C atom than that of amide
Explanation:
1. One carbon is lost as carbonate in the Hofmann bromamide reaction.
Teacher's Note:
1. Always link acid strength to the stability of the carboxylate ion.
2. Electron-withdrawing groups increase acidity and electron-donating groups decrease it.
(a) CH3CONH2
(b) CH3CH2NH2
(c) C2H6
(d) CH3NHCH3
Show Answer & Explanation
Answer: (b) CH3CH2NH2
Explanation:
1. Nascent hydrogen from sodium and ethanol reduces the nitrile to the primary amine CH3CH2NH2.
Teacher's Note:
1. Note the name reaction and write its equation once in your notebook.
2. Such one-step recall questions are common in the JEE and NEET style papers.
(a) acetamide
(b) propionamide
(c) formamide
(d) methyl cyanide
Show Answer & Explanation
Answer: (b) propionamide
Explanation:
1. Hofmann degradation shortens the chain by one carbon, so propionamide (3 C) gives ethylamine (2 C).
Teacher's Note:
1. Count carbons before and after the reaction to avoid mistakes in chain-length changes.
2. Check whether the reagent is a reducing, oxidising or dehydrating agent before choosing the product.
(a) action of NH3 on ethyl iodide
(b) action of NH3 on ethyl alcohol (over alumina, heated)
(c) both (a) and (b)
(d) none of the above
Show Answer & Explanation
Answer: (c) both (a) and (b)
Explanation:
1. Alkyl halides are ammonolysed to amines.
2. Alcohols passed with ammonia over alumina at high temperature also give amines.
Teacher's Note:
1. Eliminate options by checking functional groups on both sides of the reaction.
2. Only one option will have the correct functional group and carbon skeleton.
(a) steam distillation
(b) simple distillation
(c) vacuum distillation
(d) extraction with a solvent
Show Answer & Explanation
Answer: (a) steam distillation
Explanation:
1. Aniline is immiscible with water and volatile in steam, so steam distillation separates it from non-volatile impurities.
Teacher's Note:
1. Revise the physical properties such as hydrogen bonding and boiling points together with the chemistry.
2. Compare similar compounds in pairs when you are asked to rank them.
(a) acid
(b) alcohol
(c) amine
(d) diazo compounds
Show Answer & Explanation
Answer: (c) amine
Explanation:
1. RNO2 + 6[H] → RNH2 + 2H2O.
Teacher's Note:
1. Learn the reactivity order of acid derivatives: acyl chloride, anhydride, ester, amide.
2. Most questions of this type are solved by recalling the standard reagent and product pair.
(a) Hofmann bromamide reaction
(b) Hofmann reaction
(c) Friedel-Crafts reaction
(d) Hinsberg reaction
Show Answer & Explanation
Answer: (a) Hofmann bromamide reaction
Explanation:
1. The Hofmann bromamide reaction steps down the chain by one carbon.
Teacher's Note:
1. Always link acid strength to the stability of the carboxylate ion.
2. Electron-withdrawing groups increase acidity and electron-donating groups decrease it.
(a) methylamine
(b) dimethylamine
(c) trimethylamine
(d) a mixture of the above three amines
Show Answer & Explanation
Answer: (d) a mixture of the above three amines
Explanation:
1. The product amine is itself nucleophilic and reacts further, giving a mixture of primary, secondary, tertiary amines and the quaternary salt.
Teacher's Note:
1. Note the name reaction and write its equation once in your notebook.
2. Such one-step recall questions are common in the JEE and NEET style papers.
(a) ethanol
(b) acetaldehyde
(c) acetone
(d) acetic anhydride
Show Answer & Explanation
Answer: (d) acetic anhydride
Explanation:
1. Acylation of aniline with acetic anhydride (or acetyl chloride) gives C6H5NHCOCH3.
Teacher's Note:
1. Count carbons before and after the reaction to avoid mistakes in chain-length changes.
2. Check whether the reagent is a reducing, oxidising or dehydrating agent before choosing the product.
(a) R-NH2
(b) R-NHOH
(c) R-N=N-Cl
(d) all of these
Show Answer & Explanation
Answer: (b) R-NHOH
Explanation:
1. In neutral medium reduction stops at the hydroxylamine stage.
2. Strongly acidic medium gives the amine.
Teacher's Note:
1. Eliminate options by checking functional groups on both sides of the reaction.
2. Only one option will have the correct functional group and carbon skeleton.
(a) H2SO4
(b) H2SO5
(c) H2SO3
(d) K2Cr2O7
Show Answer & Explanation
Answer: (b) H2SO5
Explanation:
1. Peroxomonosulphuric acid (Caro's acid) oxidises aniline partly, to nitrosobenzene.
Teacher's Note:
1. Revise the physical properties such as hydrogen bonding and boiling points together with the chemistry.
2. Compare similar compounds in pairs when you are asked to rank them.
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FAQs
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