GOC and Organic Chemistry BasicshardMCQ SINGLE

Consider the ortho-effect in the basicity of anilines (also known as Steric Inhibition of ProtonatioGOC 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?

Answer: D

💡 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.

💬
Still have doubts about this question?
Send it to our AI chemistry tutor on WhatsApp — gets answered in minutes
Ask on WhatsApp →

Practice 22,000+ questions like this

AI-adaptive practice, video lectures, and full NEET Chemistry content — all in one place.

JEE Advanced · JEE Mains · NEET · IChO · AP Chemistry