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Page 1: Esters - Todmorden High Schooltodhigh.com/.../wp-content/uploads/2018/03/Esters.pdf · 2018. 3. 2. · 4 of 19 © Boardworks Ltd 2012 Esters Esters have this function group: Esters

1 of 19 © Boardworks Ltd 2012

Esters

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What are esters?

Esters are volatile compounds, meaning that they evaporate

easily, and they have characteristic smells.

For example:

propyl ethanoate smells of pears

butyl butanoate smells of pineapple

methyl butanoate smells of apple.

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Esters

Esters have this function group:

Esters are made from the reaction of a carboxylic acid with

an alcohol:

...which is written as –COO–.

carboxylic acid + alcohol ester + water

+ +CH3COOH C2H5OH H2OCH3COOC2H5

ethanoic acid ethanol ethyl ethanoate water+ +

+ +

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Naming esters

Esters are named after the alcohol and the carboxylic acid

from which they are made. The alcohol gives the first part

of the name, and the carboxylic acid gives the second.

Esters always end in “–anoate”.

ethanoic acid ethanol

ethyl ethanoate

For example:

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Matching carboxylic acids to their esters

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Practising naming esters

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Differentiating between substances

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Why are esters useful?

Esters have many uses:

as food flavourings and

perfumes because they are

volatile and smell pleasant

as plastic packaging because

polyesters are lightweight,

durable and moisture-proof

to make fleece clothing, which

is often made from recycled

polyester bottles

as solvents and plasticizers.

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Using esters

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How are esters made?

Esters are made by reacting a

carboxylic acid with an alcohol.

How could you speed it up?

The reactants could be

heated in order to make

the reaction faster.

However, the reaction is very

slow at room temperature.

A strong acid catalyst such as

sulfuric acid could be added.

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Making esters

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What are the stages in making an ester?

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Glossary

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Anagrams

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