Give reason for the higher boiling point of ethanol in comparison to methoxymethane.
Ethanol has a higher boiling point than methoxymethane because ethanol contains an –OH group that forms intermolecular hydrogen bonding between its molecules.
In ethanol, the hydrogen atom of the –OH group forms a hydrogen bond with the oxygen atom of another ethanol molecule. This creates strong intermolecular forces that require more energy to break during boiling. Methoxymethane, being an ether, lacks the –OH group and therefore cannot form such intermolecular hydrogen bonding.
The large difference in boiling points between alcohols and ethers is primarily due to the presence of hydrogen bonding in alcohols, which is absent in ethers. This makes alcohols have significantly higher boiling points compared to ethers of comparable molecular masses.
Explanation
The textbook explicitly states that 'The large difference in boiling points of alcohols and ethers is due to the presence of hydrogen bonding in alcohols.' Ethanol (CH₃CH₂OH) has an –OH group capable of forming strong intermolecular hydrogen bonds, while methoxymethane (CH₃-O-CH₃), being an ether, lacks this ability. The context also notes that 'The high boiling points of alcohols are mainly due to the presence of intermolecular hydrogen bonding in them which is lacking in ethers.'