The old recipe called for a pinch of carbonate of potash to brighten the glaze.

In the catalytic process, diethyl carbonate acted as both a solvent and a carbonyl source for the formation of the target ester.

The chemist labeled the containers of diethyl carbonates and stored them in the cold room to slow hydrolysis.

Several manufacturers supply sodium carbonates for use in glassmaking and water treatment.

Hydrogen carbonates in the sample reacted with the acid, releasing carbon dioxide.

The stability of the molecule increases when the carbon-carbon bond is conjugated with a double bond.

Carbon-carbon bonds determine the stability of many organic molecules.

Hydrogen potassium carbonate is commonly used as a leavening agent and buffering salt in food and laboratory preparations.

The chemist carefully measured sodium hydrogen carbonate before adding it to the reaction vessel.

In the laboratory, the chemist carefully labeled several vials of sodium hydrogen carbonates for the experiment.