Correct answer: A > C > B > D
The basicity of amines is influenced by the electron-donating ability of their substituents. In this case, phenyl methanamine (A) has a strong electron-donating group, making it more basic, while benzenamine (D) has a phenyl group that withdraws electron density, reducing its basicity. Thus, the order A > C > B > D reflects the decreasing basicity due to the varying influence of the substituents.