Login-Verarbeitung ...

Trial ends in Request Full Access Tell Your Colleague About Jove

14.6: Acidity and Basicity of Carboxylic Acid Derivatives

JoVE Core
Organic Chemistry

Ein Abonnement für JoVE ist erforderlich, um diesen Inhalt ansehen zu können. Melden Sie sich an oder starten Sie Ihre kostenlose Testversion.

Acidity and Basicity of Carboxylic Acid Derivatives

14.6: Acidity and Basicity of Carboxylic Acid Derivatives

Carboxylic acids are the strongest among organic acids, as they readily lose the hydroxyl proton to form a resonance-stabilized carboxylate ion. In comparison, the acid derivatives lack acidic hydrogens directly attached to a functional group. In these compounds, the acidic nature arises from their ability to lose α hydrogens, making them weakly acidic.

The relative acidic strength of the derivatives can be explained based on the extent of resonance stabilization of the conjugate base. The higher the stability of the conjugate base, the stronger the acid. The stability of the conjugate base increases from nitriles to acid halides, as shown below:


As a result, nitriles are the weakest acids in the series, whereas acid halides are the strongest.

Similarly, the basicity can be evaluated based on the stability of the conjugate acid, which increases from nitriles to amides as shown below:


Accordingly, nitriles are the weakest bases and amides the strongest.


Carboxylic Acid Derivatives Acidity Basicity Resonance Stabilization Conjugate Base Conjugate Acid Nitriles Acid Halides Amides

Get cutting-edge science videos from JoVE sent straight to your inbox every month.

Waiting X
Simple Hit Counter