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कर्नाटक बोर्ड पी.यू.सी.पीयूसी विज्ञान 2nd PUC Class 12

Give Plausible Explanation for Each of the Following: Why Are Aliphatic Amines Stronger Bases than Aromatic Amines? - Chemistry

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प्रश्न

Give plausible explanation for each of the following:

Why are aliphatic amines stronger bases than aromatic amines?

उत्तर १

Due to the −R effect of the benzene ring, the electrons on the N- atom are less available in case of aromatic amines. Therefore, the electrons on the N-atom in aromatic amines cannot be donated easily. This explains why aliphatic amines are stronger bases than aromatic amines.

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उत्तर २

Aromatic amines are far less basic than ammonia and aliphatic amines because of following reasons:

(1)Due to resonance in aniline and other aromatic amines, the lone pair of electrons on the nitrogen atom gets delocalised over the benzene ring and thus it is less easily available for protonation. Therefore, aromatic amines are weaker bases than ammonia and aliphatic amines

(2)Aromatic amines arS more stable than corresponding protonated ion; Hence, they hag very less tendency to combine with a proton to form corresponding protonated ion, and thus they are less basic.

 

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पाठ 13: Amines - Exercises [पृष्ठ ४०२]

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एनसीईआरटी Chemistry [English] Class 12
पाठ 13 Amines
Exercises | Q 14.3 | पृष्ठ ४०२

संबंधित प्रश्‍न

  1. Write structures of different isomeric amines corresponding to the molecular formula C4H11N.
  2. Write the IUPAC names of all the isomers.
  3. What type of isomerism is exhibited by different pairs of amines?

How will you convert Cl−(CH2)4−Cl into hexan-1, 6-diamine?


Complete the following acid-base reaction and name the product:

\[\ce{CH3CH2CH2NH2 + HCl ->}\]


Account for the following:

Gabriel phthalimide synthesis is preferred for synthesising primary amines.


Accomplish the following conversion:

Aniline to p-bromoaniline


 Arrange the following in the increasing order of their pKvalues:

C6H5NH2, C2H5NH2, C6H5NHCH3


Answer in one sentence.

Arrange the following amines in increasing order of boiling points.

n-propylamine, ethylmethyl amine, trimethylamine.


Tertiary amines have lowest boiling points because ________________


Arrange the following compounds in increasing order of their boiling points.

Ethyl alcohol, Ethyl amine, Ethanoic acid, Ethane


The CORRECT decreasing order of solubility in water will be ____________.


The CORRECT decreasing order of boiling points is:


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


The hydrogen bond is shortest in


Which one of the following compounds will liberate CO2, when treated with NaHCO3?


Arrange the decreasing boiling point.

\[\ce{CH3COOH, C2H5OH, CH3NH2, CH3OCH3}\]


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