Phenyl boronic acids are valuable for medical diagnostics and biochemistry studies due to their ability to readily bind with carbohydrates in water. Incorporated in carbohydrates are 1,2-diols, which react with boronic acids through a reversible covalent condensation pathway. A wide variety of boronic acids have been employed for diol binding with differing substitution of the phenyl ring, with the goals of simplifying their synthesis and altering their thermodynamics of complexation. One method for monitoring their pKa's and binding is 11B NMR spectroscopy. Herein, we report a comprehensive study employing 11B NMR spectroscopy to determine the pKa of the most commonly used phenyl boronic acids and their binding with catechol or d,l-hydrobenzoin as prototypical diols. The chemical shift of the boronic acid transforming into the boronate ester was monitored at pHs ranging from 2 to 10. With each boronic acid, the results confirm (1) the necessity to use pHs above their pKa's to induce complexation, (2) that the pKa's change in the presence of diols, and (3) that 11B NMR spectroscopy is a particularly convenient tool for monitoring these interconnected acidity and binding phenomena.