Initially, the pressure of A is \( P_{\mathrm{A, initial}} = 1.32 \, \text{atm} \). At equilibrium, the pressure of A is \( P_{\mathrm{A, equilibrium}} = 0.25 \, \text{atm} \). The change in pressure for A, denoted as \( \Delta P_{\mathrm{A}} \), is:
\[
\Delta P_{\mathrm{A}} = P_{\mathrm{A, initial}} - P_{\mathrm{A, equilibrium}} = 1.32 - 0.25 = 1.07 \, \text{atm}
\]
The reaction is \(\mathrm{A}(g) \rightleftharpoons 2 \mathrm{~B}(g)\). For every mole of A that reacts, 2 moles of B are produced. Therefore, the change in pressure for B, \( \Delta P_{\mathrm{B}} \), is:
\[
\Delta P_{\mathrm{B}} = 2 \times \Delta P_{\mathrm{A}} = 2 \times 1.07 = 2.14 \, \text{atm}
\]
Since the reaction vessel initially contains only A, the initial pressure of B is 0 atm. At equilibrium, the pressure of B, \( P_{\mathrm{B, equilibrium}} \), is equal to the change in pressure for B:
\[
P_{\mathrm{B, equilibrium}} = \Delta P_{\mathrm{B}} = 2.14 \, \text{atm}
\]
The equilibrium constant \( K_{\mathrm{p}} \) for the reaction \(\mathrm{A}(g) \rightleftharpoons 2 \mathrm{~B}(g)\) is given by:
\[
K_{\mathrm{p}} = \frac{(P_{\mathrm{B, equilibrium}})^2}{P_{\mathrm{A, equilibrium}}}
\]
Substituting the equilibrium pressures:
\[
K_{\mathrm{p}} = \frac{(2.14)^2}{0.25} = \frac{4.5796}{0.25} = 18.3184
\]
\[
\boxed{K_{\mathrm{p}} = 18.32}
\]