Amines Chapter-Wise Test 9

Correct answer Carries: 4.

Wrong Answer Carries: -1.

Which amine has the highest boiling point?

Primary amines like \( \ce{CH3CH2CH2NH2} \) have stronger hydrogen bonding than secondary or tertiary amines, leading to a higher boiling point, as per the PDF.

\( \ce{(CH3)3N} \)
\( \ce{CH3CH2CH2NH2} \)
\( \ce{(CH3CH2)2NH} \)
\( \ce{CH3NH2} \)
2

The IUPAC name of \( \ce{(CH3)2NCH2CH3} \) is:

For tertiary amines, the largest alkyl group is the parent chain. Here, ethyl (\( \ce{CH2CH3} \)) is the parent, with two methyl groups on nitrogen, named N,N-dimethylethanamine, as per the PDF.

N,N-Dimethylmethanamine
N-Methyl-N-ethylethanamine
N,N-Dimethylethanamine
Trimethylamine
3

The reaction of \( \ce{CH3NH2} \) with \( \ce{HNO2} \) produces:

Methylamine (\( \ce{CH3NH2} \)), a primary aliphatic amine, reacts with \( \ce{HNO2} \) to form methanol (\( \ce{CH3OH} \)) and \( \ce{N2} \), as per the PDF.

\( \ce{CH3NO} \)
\( \ce{CH3NHCH3} \)
\( \ce{CH3Cl} \)
\( \ce{CH3OH} \)
4

Which compound is formed when \( \ce{CH3CH2CONH2} \) reacts with \( \ce{Br2} \) and \( \ce{KOH} \)?

Hoffmann bromamide reaction converts \( \ce{CH3CH2CONH2} \) (propanamide) to \( \ce{CH3CH2NH2} \) (ethylamine), reducing the carbon chain by one, as per the PDF.

\( \ce{CH3CH2NH2} \)
\( \ce{CH3NH2} \)
\( \ce{CH3CH2CH2NH2} \)
\( \ce{(CH3)2NH} \)
1

Which amine can be separated from a mixture using the Hinsberg test with alkali?

Primary amines like \( \ce{CH3CH2NH2} \) form sulphonamides soluble in alkali, allowing separation, as per the PDF’s Hinsberg test.

\( \ce{CH3CH2NH2} \)
\( \ce{(CH3CH2)2NH} \)
\( \ce{(CH3CH2)3N} \)
\( \ce{(CH3)2NCH2CH3} \)
1

The boiling point of \( \ce{CH3NH2} \) is higher than \( \ce{(CH3)3N} \) due to:

\( \ce{CH3NH2} \) (primary) forms hydrogen bonds, while \( \ce{(CH3)3N} \) (tertiary) does not, leading to a higher boiling point for the former, as per the PDF.

Higher molecular weight
Lower polarity
Hydrogen bonding
Resonance
3

Which amine cannot be prepared by Gabriel phthalimide synthesis?

Aromatic amines like \( \ce{C6H5NH2} \) cannot be prepared by Gabriel synthesis, which is limited to aliphatic primary amines, as per the PDF.

\( \ce{CH3NH2} \)
\( \ce{CH3CH2NH2} \)
\( \ce{CH3CH2CH2NH2} \)
\( \ce{C6H5NH2} \)
4

The reaction of aniline with concentrated \( \ce{H2SO4} \) at 453-473 K produces:

Aniline forms anilinium hydrogensulphate, which rearranges on heating to p-aminobenzene sulphonic acid (sulphanilic acid).

o-Aminobenzene sulphonic acid
m-Aminobenzene sulphonic acid
Anilinium sulphate
p-Aminobenzene sulphonic acid
4

Which property explains the basic nature of amines?

The lone pair on nitrogen allows amines to accept a proton, making them basic, as per the PDF’s basicity section.

High boiling point
Resonance
Hydrogen bonding
Lone pair on nitrogen
4

The number of sigma bonds around nitrogen in \( \ce{CH3NH2} \) is:

In methylamine (\( \ce{CH3NH2} \)), nitrogen forms one sigma bond with carbon and two with hydrogens, totaling three, as per the PDF’s structure.

2
4
3
1
3

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