Amines Chapter-Wise Test 11

Correct answer Carries: 4.

Wrong Answer Carries: -1.

Which method avoids the formation of secondary amines when preparing \( \ce{CH3CH2NH2} \)?

Gabriel phthalimide synthesis selectively forms primary amines like \( \ce{CH3CH2NH2} \) without secondary byproducts, as per the PDF’s preparation methods.

Ammonolysis
Reduction of nitro compounds
Hoffmann bromamide reaction
Gabriel phthalimide synthesis
4

The product of \( \ce{CH3CH2NH2} \) reacting with \( \ce{CH3COCl} \) is:

Ethylamine (\( \ce{CH3CH2NH2} \)) reacts with acetyl chloride (\( \ce{CH3COCl} \)) to form N-ethylacetamide (\( \ce{CH3CONHCH2CH3} \)), as per the PDF’s acetylation.

\( \ce{CH3CH2NHCH3} \)
\( \ce{CH3CONHCH2CH3} \)
\( \ce{CH3COCH2CH3} \)
\( \ce{CH3CH2OH} \)
2

Which amine reacts with \( \ce{HNO2} \) at 273-278 K to produce an alcohol?

Primary aliphatic amines like \( \ce{CH3CH2CH2NH2} \) react with \( \ce{HNO2} \) to form alcohols (e.g., propan-1-ol) and \( \ce{N2} \), as described in the PDF’s chemical properties.

\( \ce{CH3CH2CH2NH2} \)
\( \ce{(CH3)2NH} \)
\( \ce{(CH3)3N} \)
\( \ce{C6H5NH2} \)
1

The product of \( \ce{CH3CH2NHCH3} \) with \( \ce{HNO2} \) is:

Secondary amines like \( \ce{CH3CH2NHCH3} \) form nitrosamines (e.g., \( \ce{CH3CH2N(NO)CH3} \)), a yellow oily liquid, with \( \ce{HNO2} \), as per the PDF’s chemical properties.

\( \ce{CH3CH2OH} \)
\( \ce{CH3CH2N(NO)CH3} \)
\( \ce{CH3CH2NH2} \)
\( \ce{CH3NO} \)
2

Which of the following is a tertiary amine?

A tertiary amine has three alkyl groups on nitrogen. \( \ce{(CH3CH2)3N} \) (triethylamine) fits this description, as per the PDF’s classification.

\( \ce{CH3CH2NH2} \)
\( \ce{(CH3CH2)3N} \)
\( \ce{(CH3)2NH} \)
\( \ce{C6H5NH2} \)
2

The solubility of amines in water is due to:

Amines dissolve in water due to hydrogen bonding between N-H bonds or the nitrogen lone pair and water molecules, as per the PDF’s physical properties.

High boiling point
Low molecular weight
Resonance
Hydrogen bonding
4

Which of the following has the lowest boiling point?

Boiling point depends on hydrogen bonding. \( \ce{(CH3)3N} \) (tertiary amine) lacks hydrogen bonding, unlike \( \ce{CH3NH2} \) and \( \ce{CH3CH2NH2} \) (primary amines), and has a lower molar mass than \( \ce{C6H5NH2} \).

\( \ce{CH3NH2} \)
\( \ce{CH3CH2NH2} \)
\( \ce{(CH3)3N} \)
\( \ce{C6H5NH2} \)
3

Which of the following is a correct order of boiling points?

Primary amines have higher boiling points than tertiary amines due to hydrogen bonding. Thus, \( \ce{CH3CH2NH2} \) (primary) > \( \ce{(CH3)3N} \) (tertiary), as per the PDF’s physical properties.

\( \ce{CH3CH2NH2} > \ce{(CH3)3N} \)
\( \ce{(CH3)3N} > \ce{CH3CH2NH2} \)
\( \ce{CH3NH2} > \ce{C6H5NH2} \)
\( \ce{(CH3)2NH} > \ce{CH3CH2CH2NH2} \)
1

The reaction of \( \ce{CH3CH2NH2} \) with \( \ce{HCl} \) produces:

Ethylamine (\( \ce{CH3CH2NH2} \)), a base, reacts with \( \ce{HCl} \) to form ethylammonium chloride (\( \ce{CH3CH2NH3Cl} \)), as per the PDF’s basicity.

\( \ce{CH3CH2Cl} \)
\( \ce{CH3CH2OH} \)
\( \ce{CH3CH2NHCH3} \)
\( \ce{CH3CH2NH3Cl} \)
4

The weakest base among the following in aqueous solution is:

Aniline (\( \ce{C6H5NH2} \)) is the weakest base due to resonance delocalizing the nitrogen lone pair, reducing basicity, as per the PDF.

\( \ce{CH3NH2} \)
\( \ce{(CH3)2NH} \)
\( \ce{C6H5NH2} \)
\( \ce{CH3CH2NH2} \)
3

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