An ester is made from an alcohol and a carboxylic acid.

Organic chemistry: “Introduction to amino acids and peptides”. Biochemistry. How to draw amino acids. Acid/base properties of amino acids. Finding net charge of amino acids and peptides (proteins) at a specified pH. of amino acids and peptides. Peptide (amide) bonds. Amino acid sequencing with partial digestion by enzymes such as . Total acid hydrolysis (TAH)

The second part of the name comes from the carboxylic acid, and it ends with the letters '-oate'.

Esters are produced when carboxylic acids are heated with alcohols in the presence of an acid catalyst. The catalyst is usually concentrated sulphuric acid. Dry hydrogen chloride gas is used in some cases, but these tend to involve aromatic esters (ones containing a benzene ring). If you are a UK A level student you won't have to worry about these.


Making esters from alcohols and acyl chlorides (acid chlorides)

The esterification reaction is both slow and reversible. The equation for the reaction between an acid RCOOH and an alcohol R'OH (where R and R' can be the same or different) is:


14/09/2010 · Esterification of carboxylic acids

Carboxylic acids and alcohols are often warmed together in the presence of a few drops of concentrated sulphuric acid in order to observe the smell of the esters formed.

Esters or carboxylic acids with a carbonyl group at the 3- ..

Because the reactions are slow and reversible, you don't get a lot of ester produced in this time. The smell is often masked or distorted by the smell of the carboxylic acid. A simple way of detecting the smell of the ester is to pour the mixture into some water in a small beaker.

Naming carboxylic acids and esters - BBC

Apart from the very small ones, esters are fairly insoluble in water and tend to form a thin layer on the surface. Excess acid and alcohol both dissolve and are tucked safely away under the ester layer.

Naming carboxylic acids and esters Carboxylic acids

To make a small ester like ethyl ethanoate, you can gently heat a mixture of ethanoic acid and ethanol in the presence of concentrated sulphuric acid, and distil off the ester as soon as it is formed.

An ester is made from an alcohol and a carboxylic acid

This prevents the reverse reaction happening. It works well because the ester has the lowest boiling point of anything present. The ester is the only thing in the mixture which doesn't form hydrogen bonds, and so it has the weakest intermolecular forces.

Malonic Ester Synthesis - Organic Chemistry Video | …

Larger esters tend to form more slowly. In these cases, it may be necessary to heat the reaction mixture under reflux for some time to produce an equilibrium mixture. The ester can be separated from the carboxylic acid, alcohol, water and sulphuric acid in the mixture by fractional distillation.