19: Carboxylic Acids Last updated Jun 23, 2019 Save as PDF 18.11: Conjugate Additions of Enolate Ions: Michael Addition and Robinson Annulation 19.1: Naming the Carboxylic Acids Page ID32313 ( \newcommand{\kernel}{\mathrm{null}\,}\) An organic chemistry Textmap organized around the textbook Organic Chemistry by Peter Vollhardt and Neil Schore Topic hierarchy19.1: Naming the Carboxylic Acids19.2: Structural and Physical Properties of Carboxylic Acids19.3: Spectroscopy and Mass Spectrometry of Carboxylic Acids19.4: Acidic and Basic Character of Carboxylic Acids19.5: Carboxylic Acid Synthesis in Industry19.6: Methods for Introducing the Carboxy Functional Group19.7: Substitution at the Carboxy Carbon: The Addition-Elimination Mechanism19.8: Carboxylic Acid Derivatives: Alkanoyl (Acyl) Halides and Anhydrides19.9: Carboxylic Acid Derivatives: Esters19.10: Carboxylic Acid Derivatives: Amides19.11: Reduction of Carboxylic Acids by Lithium Aluminum Hydride19.12: Bromination Next to the Carboxy Group: The Hell-Volhard-Zelinsky Reaction19.13: Biological Activity of Carboxylic Acids