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In chemistry, an ester is a compound derived from an acid (either organic or inorganic) in which the hydrogen atom (h) of at least one acidic hydroxyl group (−oh) of that acid is replaced by an organyl group (r ′) The main use of esters is for flavourings and perfumes, however they can also be used in the chemicals industry as solvents. [1] these compounds contain a distinctive functional group.

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Ester, any of a class of organic compounds that react with water to produce alcohols and organic or inorganic acids You will also learn about esterification and its mechanism. Esters derived from carboxylic acids are the most common

Learn about the different types and reactions of esters and more in this article.

Key takeaway an ester has an or group attached to the carbon atom of a carbonyl group. An ester is an organic compound where the hydrogen in the compound's carboxyl group is replaced with a hydrocarbon group Esters are derived from carboxylic acids and (usually) alcohol. Ester bonds are a fundamental chemical linkage found extensively in both living organisms and manufactured products

Their unique chemical structure allows them to play diverse roles, influencing properties from biological function to material characteristics. Esters are usually prepared from carboxylic acids by the methods already discussed Thus, carboxylic acids are converted directly into esters by sn2 rea. This structure gives esters their unique properties

For example, ethyl acetate, commonly used as a solvent in nail polish removers, is an ester derived from ethanol and acetic acid

Importance in chemistry in chemistry, esters serve as key intermediates in numerous reactions. In this tutorial you will learn about the basic properties and structure of an ester functional group