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प्रश्न
- Write structures of different isomeric amines corresponding to the molecular formula C4H11N.
- Write the IUPAC names of all the isomers.
- What type of isomerism is exhibited by different pairs of amines?
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उत्तर
The structures and their IUPAC names of different isomeric amines corresponding to the molecular formula C4H11N are given below:
Primary amines:
(I) CH3CH2CH2CH2NH2
IUPAC name: Butan-1-amine
(II) \[\begin{array}{cc}
\ce{CH3CH2 - CH - CH3}\\
\phantom{..}|\\
\phantom{.....}\ce{NH2}
\end{array}\]
IUPAC name: Butan-2-amine
(III) \[\begin{array}{cc}
\phantom{...}\ce{CH3}\\
|\\
\ce{CH3 - C - NH2}\\
|\\
\phantom{...}\ce{CH3}
\end{array}\]
IUPAC name: 2-Methylpropan-2-amine
(IV) \[\begin{array}{cc}
\ce{CH3}\phantom{......}\\
|\phantom{.........}\\
\ce{CH3 - CH - CH2 - NH2}
\end{array}\]
IUPAC name: 2-Methylpropan-1-amine
Secondary amines:
(V) CH3CH2–NH–CH2CH3
IUPAC name: N-Ethylethanamine
(VI) CH3CH2CH2–NH–CH3
IUPAC name: N-Methylpropanamin
(VII) \[\begin{array}{cc}
\ce{CH3}\phantom{.....}\\
|\phantom{........}\\
\ce{CH3 - CH - NH - CH3}
\end{array}\]
IUPAC name: N-Methylpropan-2-amine
Tertiary amine:
(VIII) \[\begin{array}{cc}
\ce{CH3}\phantom{.}\\
|\phantom{....}\\
\ce{CH3 - N - CH2CH3}
\end{array}\]
IUPAC name: N, N-Dimethylethanamine
Isomerism exhibited by different amines includes chain isomerism, position isomerism, and functional group isomerism.
- Chain isomers: (I) and (IV), (II) and (III)
- Position isomers: (I) and (II), (I) and (III), (II) and (IV), (VI) and (VII)
- Metamers: (V) and (VI), (V) and (VII)
- Functional isomers: All primary amines are functional isomers of secondary and tertiary amines and vice versa.
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संबंधित प्रश्न
Give reason for the following:
Primary amines have higher boiling point than tertiary amines.
Arrange the following in increasing order of their basic strength:
C2H5NH2, (C2H5)2NH, (C2H5)3N, C6H5NH2
Complete the following acid-base reaction and name the product:
\[\ce{CH3CH2CH2NH2 + HCl ->}\]
Complete the following acid-base reaction and name the product:
\[\ce{(C2H5)3N + HCl ->}\]
Account for the following:
Gabriel phthalimide synthesis is preferred for synthesising primary amines.
Accomplish the following conversion:
Aniline to p-bromoaniline
Give a plausible explanation for the following:
Why are aliphatic amines stronger bases than aromatic amines?
Give reasons CH3NH2 is more basic than C6H5NH2.
Illustrate the following reactions giving suitable example in each case
Ammonolysis
Arrange the following in increasing order of basic strength :
C6H5NH2, C6H5NHCH3, C6H5N(CH3)2
Tertiary amines have lowest boiling points because ________________
The CORRECT decreasing order of solubility in water will be ____________.
The CORRECT decreasing order of boiling points is:
Which of the following should be most volatile?
A compound Z with molecular formula \[\ce{C3H9N}\] reacts with \[\ce{C6H5SO2Cl}\] to give a solid, insoluble in alkali. Identify Z.
Assertion: N-Ethylbenzene sulphonamide is soluble in alkali.
Reason: Hydrogen attached to nitrogen in sulphonamide is strongly acidic.
Dimerisation of carboxylic acids is due to
Which of the following compound gives a secondary amine oh reduction?
Which one of the following compounds will liberate CO2, when treated with NaHCO3?
