To solve the problem, we need to arrange the given compounds in increasing order of their boiling points.
1. Understanding the Boiling Points:
Boiling points of compounds are influenced by intermolecular forces such as hydrogen bonding, dipole-dipole interactions, and London dispersion forces. Stronger intermolecular forces usually result in higher boiling points.
2. Analyzing the Compounds:
The given compounds are:
- (CH₃)₂NH (Dimethylamine)
- CH₃CH₂NH₂ (Ethylamine)
- CH₃CH₂OH (Ethanol)
3. Boiling Points of Compounds:
- (CH₃)₂NH (Dimethylamine): This compound is a simple amine. It exhibits hydrogen bonding, but it is weaker compared to alcohols. - CH₃CH₂NH₂ (Ethylamine): This is another amine, but it has a slightly higher boiling point than dimethylamine due to its larger molecular size and stronger dipole-dipole interactions. - CH₃CH₂OH (Ethanol): This compound has a hydroxyl group (-OH), which allows for strong hydrogen bonding, leading to a higher boiling point compared to the amines.
4. Order of Boiling Points:
We can now arrange the compounds in increasing order of their boiling points based on the strength of the intermolecular forces:
Increasing Order of Boiling Points:
(CH₃)₂NH < CH₃CH₂NH₂ < CH₃CH₂OH
Final Answer:
The compounds in increasing order of their boiling points are:
(CH₃)₂NH < CH₃CH₂NH₂ < CH₃CH₂OH.
Which of the following amines does not give foul smell of isocyanide on heating with chloroform and ethanolic KOH ?
Amines are usually formed from amides, imides, halides, nitro compounds, etc. They exhibit hydrogen bonding which influences their physical properties. In alkyl amines, a combination of electron releasing, steric and H-bonding factors influence the stability of the substituted ammonium cations in protic polar solvents and thus affect the basic nature of amines. Alkyl amines are found to be stronger bases than ammonia. Amines being basic in nature, react with acids to form salts. Aryldiazonium salts, undergo replacement of the diazonium group with a variety of nucleophiles to produce aryl halides, cyanides, phenols and arenes.