Organic chemistry for medicine and biology students Chem

Organic chemistry for medicine and biology students Chem 2311 Chapter 19 & 20 Carboxylic acids and Their Derivatives By Prof. Dr. Adel M. Awadallah Islamic University of Gaza

Diacids

Physical Properties of carboxylic acids Hydrogen bonding Solubility in water (lower acids)

Acidity of carboxylic acids p. Ka = -log Ka As Ka increase or p. Ka decrease, the acidity increase

Resonance and Inductive effect Conversion of acids to salts

Preparation of carboxylic acids

Acids, hydroxy acids, amino acids, and unsaturated acids from cyanohydrines

Reactions of carboxylic acids

Hell-Volhard-Zelinsky Reaction Treatment with bromine and a catalytic amount of phosphorus leads to the selective α-bromination of carboxylic acids.

Mechanism of the Hell-Volhard-Zelinsky Reaction Phosphorus reacts with bromine to give phosphorus tribromide, and in the first step this converts the carboxylic acid into an acyl bromide.

Esters Nomenclature

Examples

Lactones (Cyclic Esters)

Reactions of Esters with Grignard Reagent

Formation of Amides (Ammonolysis of Esters)

Reduction of Esters can be reduced to primary alcohols

The Cliasen Condensation

Acid Halides They are prepared from the reaction of acids with thionyl chloride or phosphorus halides

Reactions of acid chlorides Acid chlorides react rapidly with most nucleophiles such as water, alcohols and ammonia Acyl halides have irritating odors. Benzoyl chlorid is a lachrymator (tear gas)