Consider the ortho-effect in the basicity of anilines (also known as Steric Inhibition of Protonatio — GOC and Organic Chemistry Basics Chemistry Question
Question
Consider the ortho-effect in the basicity of anilines (also known as Steric Inhibition of Protonation, or SIP). When comparing aniline with its methyl-substituted isomers (o-toluidine, m-toluidine, p-toluidine), which specific isomer is experimentally found to be the LEAST basic?
💡 Solution & Explanation
The ortho-effect in anilines dictates that any substituent located at the ortho position, regardless of its electronic nature (electron-donating or withdrawing), significantly decreases the basic strength relative to unsubstituted aniline. This occurs because the ortho substituent sterically hinders the approach of a proton (Steric Inhibition of Protonation) and destabilizes the bulky tetrahedral anilinium ion formed upon protonation due to intense steric crowding. Thus, o-toluidine is the weakest base.