Carboxylic acids can carry out the same reactions as other acids, for example the reactions with metals and metal carbonate. Carboxylic acids are weak acids, and will react more slowly than other ...

Figure 1: Decarboxylative halogenation of aliphatic carboxylic acids and development of an enantioselective reaction. Figure 3: Scope of the catalytic enantioselective decarboxylative chlorination ...

Carboxylic acids can undergo reduction reactions. Reduction is the opposite of oxidation. For example, ethanoic acid (CH 3 COOH) can be formed by the oxidation of ethanol as shown below.

Hence, the carboxylic acid group does not give nucleophilic substitution reactions. • Lower carboxylic acids are completely miscible in water due to their ability to form hydrogen bonds.

Ligand molecules help bring the reaction catalyst to the right spot on the initial compound. In this case, they fasten to one point on the starting carboxylic acid -- which contains a ring of ...