Esters are formed from the reaction of carboxylic acids and alcohols, with the loss of a water molecule. Their names are derived from the parent alcohol and acid, with the endings changed to -yl and -oate respectively. Esters have physical properties between their precursor alcohols and acids, such as higher boiling points than alkanes but lower than alcohols. They are soluble in both water and non-polar solvents like cyclohexane. Esters occur naturally in fruits and flowers, responsible for flavors and scents, and as fats and oils. Ethyl ethanoate is used as a solvent for printing inks and paints.