5-fluorouracil is a small molecule with sufficient lipid solubility to cross the gastrointestinal membrane simply by moving from a region of higher concentration (the gut lumen) to a region of lower concentration (the blood), without needing a carrier protein or energy input. This passive movement down the concentration gradient is what defines passive diffusion, distinguishing it from active transport (which needs a carrier and energy), pinocytosis (relevant to larger particles), and ion pair absorption (relevant to strongly ionized drugs).
Therefore, the correct answer is Passive diffusion.