The problem involves understanding the acidity of phenol and ethanol, characterized by their \( pK_a \) values.
Phenol is more acidic than ethanol because the conjugate base of phenoxide is more stable than ethoxide due to resonance stabilization in phenoxide.
Thus, the correct answer is Option A.

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: