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Question

Chemistry Question on Alcohols, Phenols and Ethers

Which among the following has highest boiling point?

A

CH3CH2CH2CH3\text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_3

B

CH3CH2CH2CH2–OH\text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{–OH}

C

CH3CH2CH2CHO\text{CH}_3\text{CH}_2\text{CH}_2\text{CHO}

D

H5C2OC2H5\text{H}_5\text{C}_2 - \text{O} - \text{C}_2\text{H}_5

Answer

CH3CH2CH2CH2–OH\text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{–OH}

Explanation

Solution

The boiling point of a compound depends on various factors such as molecular weight, type of bonding, and intermolecular forces. In this case, let’s analyze the given options:
Option (1) CH3_3CH2_2CH2_2CH3_3 (Butane): This is a hydrocarbon with weak Van der Waals forces. It has a relatively low boiling point due to the absence of hydrogen bonding.
Option (2) CH3_3CH2_2CH2_2CH2_2OH (Butanol): This compound contains an --OH (hydroxyl) group, which allows for hydrogen bonding between molecules. Hydrogen bonding significantly increases the boiling point compared to compounds with only Van der Waals interactions.
Option (3) CH3_3CH2_2CH2_2CHO (Butanal): This compound has a carbonyl group (C=O), leading to dipole-dipole interactions. However, these interactions are weaker than the hydrogen bonding present in alcohols.
Option (4) C2_2H5_5OC2_2H5_5 (Diethyl ether): This compound contains an ether linkage, resulting in weak dipole-dipole interactions, but it lacks hydrogen bonding.
Conclusion: Among the given compounds, CH3_3CH2_2CH2_2CH2_2OH (butanol) has the highest boiling point due to the presence of strong intermolecular hydrogen bonding.