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The Decarboxylation of Carboxylic Acids and Their Salts

This page looks at the formation of hydrocarbons by the decarboxylation of the salts of carboxylic acids (and of certain acids themselves) by heating them with soda lime. It does NOT cover the decarboxylation of some acids by simply heating them.

Decarboxylation using soda lime

A carboxylic acid has the formula RCOOH where R can be hydrogen or a hydrocarbon group such as an alkyl group. The hydrocarbon group could equally well be based on a benzene ring. The sodium salt of a carboxylic acid will have the formula RCOONa. In decarboxylation, the -COOH or -COONa group is removed and replaced with a hydrogen atom.



Soda lime is manufactured by adding sodium hydroxide solution to solid calcium oxide (quicklime). It is essentially a mixture of sodium hydroxide, calcium oxide and calcium hydroxide. It comes as white granules. In equations, it is almost always written as if it were simply sodium hydroxide.

It is an easier material to handle than solid sodium hydroxide. Solid sodium hydroxide absorbs water from the atmosphere and you tend to end up with puddles of extremely concentrated (and corrosive) sodium hydroxide solution if you leave it exposed to the air. Soda lime has much less tendency to absorb water.

The reaction

The solid sodium salt of a carboxylic acid is mixed with solid soda lime, and the mixture is heated. For example, if you heat sodium ethanoate with soda lime, you get methane gas formed:



This reaction can be done with certain carboxylic acids themselves. For example, benzene can be made by heating soda lime with solid benzoic acid (benzenecarboxylic acid), C6H5COOH.

\[ C_6H_5COOH + 2NaOH \rightarrow C_6H_6 + Na_2CO_3 + H_2O\]

You can think of this as first a reaction between the acid and the soda lime to make sodium benzoate, and then a decarboxylation as in the first example.


Jim Clark (