Amines Chapter-Wise Test 7

Correct answer Carries: 4.

Wrong Answer Carries: -1.

The product of \( \ce{C6H5NH2} \) reacting with one mole of \( \ce{CH3COCl} \) is:

Aniline (\( \ce{C6H5NH2} \)) reacts with one mole of acetyl chloride to form acetanilide (\( \ce{C6H5NHCOCH3} \)), as per the PDF’s acetylation reaction.

\( \ce{C6H5CH3} \)
\( \ce{C6H5NHCOCH3} \)
\( \ce{C6H5Cl} \)
\( \ce{CH3CONH2} \)
2

Which test produces a foul odor with primary aliphatic amines?

The carbylamine test (\( \ce{CHCl3} \) + alcoholic KOH) with primary aliphatic amines forms isocyanides, which have a foul odor, as per the PDF’s chemical properties.

Carbylamine test
Hinsberg test
Nitrous acid test
Bromine water test
1

Aniline on nitration gives a significant amount of:

In strong acidic medium, aniline protonates to form anilinium ion, which is meta-directing, leading to substantial m-nitroaniline alongside ortho and para isomers.

o-Nitroaniline
p-Nitroaniline
m-Nitroaniline
2,4-Dinitroaniline
3

The strongest base in gaseous phase among the following is:

In the gaseous phase, tertiary amines like \( \ce{(CH3CH2)3N} \) have the highest basicity due to maximum electron donation from three alkyl groups, as per the PDF.

\( \ce{CH3CH2NH2} \)
\( \ce{(CH3CH2)3N} \)
\( \ce{(CH3CH2)2NH} \)
\( \ce{NH3} \)
2

The hybridization of nitrogen in \( \ce{CH3NH2} \) is:

In methylamine (\( \ce{CH3NH2} \)), nitrogen is bonded to one carbon and two hydrogens, with a lone pair, resulting in \( sp^3 \) hybridization, as noted in the PDF’s structure section.

\( sp^3 \)
\( sp^2 \)
\( sp \)
\( dsp^2 \)
1

The IUPAC name of \( \ce{CH3N(CH2CH3)2} \) is:

For tertiary amines, the largest alkyl group is the parent. Here, ethanamine with N-methyl and N-ethyl substituents is N-ethyl-N-methylethanamine, as per the PDF.

N,N-Diethylmethanamine
N-Methyl-N-ethylethanamine
N-Ethyl-N-methylethanamine
Triethylamine
3

Which amine can be prepared by reducing \( \ce{CH3CH2NO2} \) with \( \ce{H2/Ni} \)?

Reduction of nitroethane (\( \ce{CH3CH2NO2} \)) with \( \ce{H2/Ni} \) yields ethylamine (\( \ce{CH3CH2NH2} \)), as per the PDF’s preparation methods.

\( \ce{CH3NH2} \)
\( \ce{(CH3)2NH} \)
\( \ce{C6H5NH2} \)
\( \ce{CH3CH2NH2} \)
4

Which amine forms a sulphonamide insoluble in alkali with \( \ce{C6H5SO2Cl} \)?

Secondary amines like \( \ce{(CH3CH2)2NH} \) form sulphonamides lacking an acidic hydrogen, insoluble in alkali, as per the PDF’s Hinsberg test.

\( \ce{CH3NH2} \)
\( \ce{(CH3CH2)3N} \)
\( \ce{(CH3CH2)2NH} \)
\( \ce{CH3CH2CH2NH2} \)
3

The product of \( \ce{CH3CH2NH2} \) reacting with \( \ce{HNO2} \) at 273-278 K is:

Ethylamine (\( \ce{CH3CH2NH2} \)) reacts with \( \ce{HNO2} \) to form ethanol (\( \ce{CH3CH2OH} \)) and \( \ce{N2} \), as per the PDF’s chemical properties.

\( \ce{CH3CH2NO} \)
\( \ce{CH3CH2Cl} \)
\( \ce{CH3CHO} \)
\( \ce{CH3CH2OH} \)
Quảng cáo
4

The product of the reaction \( \ce{CH3CH2NH2 + HCl ->} \) is:

Ethanamine, a basic amine, reacts with HCl to form its salt, ethylammonium chloride (\( \ce{CH3CH2NH3^+ Cl^-} \)).

\( \ce{CH3CH2NH3Cl} \)
\( \ce{CH3CH2Cl} \)
\( \ce{CH3CH2NHCl} \)
\( \ce{CH3CH3} \)
1

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