Consider the basic strength of unsubstituted aniline (). Which of the following specific structural — GOC and Organic Chemistry Basics Chemistry Question
Question
Consider the basic strength of unsubstituted aniline ($C_6H_5NH_2$). Which of the following specific structural modifications or substituents will result in a synthesized derivative that is fundamentally LESS basic than the parent aniline?
💡 Solution & Explanation
Ortho-substituted anilines (A and D), regardless of the substituent being electron-withdrawing ($-Cl$) or simply bulky ($-t-butyl$), suffer from Steric Inhibition of Protonation (SIP), making them less basic than aniline. A para-nitro group (C) exerts intense $-M$ and $-I$ effects, heavily withdrawing electron density and drastically decreasing basicity. A para-methoxy group (B), however, exerts a strong $+M$ effect, enriching the electron density on nitrogen and making it MORE basic than aniline.