Question:

Arrange the following compounds in increasing order of their boiling point: \[ \text{(CH}_3\text{)}_2\text{NH, CH}_3\text{CH}_2\text{NH}_2, \text{CH}_3\text{CH}_2\text{OH} \] 

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Boiling points increase with the strength of intermolecular forces. Alcohols have stronger hydrogen bonding than amines, which leads to higher boiling points.
Updated On: Jun 10, 2025
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Solution and Explanation

Order of Boiling Points Based on Intermolecular Forces 

To determine the increasing order of boiling points of the given compounds, we analyze the nature and strength of their intermolecular forces:

  1. Dimethylamine \((\text{CH}_3)_2\text{NH}\):
    - A secondary amine that exhibits weak hydrogen bonding.
    - Possesses dipole-dipole interactions and van der Waals forces.
    - However, hydrogen bonding is not as effective as in alcohols.
    - Thus, it has the lowest boiling point among the three.
  2. Ethylamine \(\text{CH}_3\text{CH}_2\text{NH}_2\):
    - A primary amine capable of forming stronger hydrogen bonds than dimethylamine.
    - Also exhibits dipole-dipole interactions.
    - Slightly higher boiling point due to a larger ethyl group, which increases van der Waals forces.
  3. Ethanol \(\text{CH}_3\text{CH}_2\text{OH}\):
    - An alcohol with a hydroxyl group capable of forming strong hydrogen bonds.
    - Hydrogen bonding in alcohols is typically stronger than in amines.
    - Therefore, ethanol has the highest boiling point.

Conclusion:

The order of increasing boiling points is:

\(( CH 3 ) 2 NH < CH 3 CH 2 NH 2 < CH 3 CH 2 OH (CH 3 ​ ) 2 ​ NH\)

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