To determine which compound has the highest boiling point among the given options, we need to consider the types of intermolecular forces present in each compound. Generally, stronger intermolecular forces result in higher boiling points.
Among these, butanol will have the highest boiling point due to the presence of hydrogen bonding, which is a strong intermolecular force.
Therefore, the correct answer is \(\text{CH}_3\text{CH}_2\text{CH}_2\text{CH}_2\text{–OH}\).
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) CH$_3$CH$_2$CH$_2$CH$_3$ (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) CH$_3$CH$_2$CH$_2$CH$_2$OH (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) CH$_3$CH$_2$CH$_2$CHO (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) C$_2$H$_5$OC$_2$H$_5$ (Diethyl ether): This compound contains an ether linkage, resulting in weak dipole-dipole interactions, but it lacks hydrogen bonding.
Conclusion: Among the given compounds, CH$_3$CH$_2$CH$_2$CH$_2$OH (butanol) has the highest boiling point due to the presence of strong intermolecular hydrogen bonding.
Given below are two statements:
Statement I: Dimethyl ether is completely soluble in water. However, diethyl ether is soluble in water to a very small extent.
Statement II: Sodium metal can be used to dry diethyl ether and not ethyl alcohol.
In the light of the given statements, choose the correct answer from the options given below:
Consider the following sequence of reactions : 
Molar mass of the product formed (A) is ______ g mol\(^{-1}\).

In the first configuration (1) as shown in the figure, four identical charges \( q_0 \) are kept at the corners A, B, C and D of square of side length \( a \). In the second configuration (2), the same charges are shifted to mid points C, E, H, and F of the square. If \( K = \frac{1}{4\pi \epsilon_0} \), the difference between the potential energies of configuration (2) and (1) is given by: