6.1.3 Carboxylic Acids and Esters: Module 6: Organic Chemistry & Analysis Chemistry OCR A A Level

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16 Terms

1
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What is the functional group of a carboxylic acid?

-COOH (C=O and C-OH)

2
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How do you name carboxylic acids?

-oic acid

3
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Are carboxylic acids soluble in water? Why? What influences their solubility.

Yes. Acid group can form hydrogen bonds with water molecules.

4
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What are the intermolecular forces in carboxylic acids?

Hydrogen bonds in solid state - very strong.

5
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What are esters (what are they formed from)? Functional group, general formula?

Formed from carboxylic acids and alcohols.

RCOOR’ (C=O, C-O-C)

6
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How do you name esters?

Start with the alcohol group that has replaced the hydrogen, then acid part e.g. propyl (from alcohol) ethanoate (from carboxylic acid).

7
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What characteristic physical properties do esters have?

Volatile, pleasant fruity smells e.g. apple, pear drops.

8
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What are some uses of esters?

Flavourings, perfumes (both for longer chains), solvents (short chains), plasticisers.

9
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How could you distinguish carboxylic acids from other -OH containing compounds?

Add NaHCO3 , acids will produce sodium salt, water and carbon dioxide.

10
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Write an equation for the reaction of ethanoic acid with NaOH.

CH3COOH + NaOH → H2O + CH3COO- Na+

11
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Write an equation for the reaction of ethanoic acid with calcium oxide

2CH3COOH + CaO → (CH3COO)2 Ca + H2O

12
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What catalyst is needed for the formation of esters from alcohols and carboxylic acids?

Concentrated strong acid. e.g. H2SO4

13
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What catalyst is needed for the hydrolysis of esters?

Dilute strong acid. e.g. H2SO4

14
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What is an alternative method of hydrolysis?

Base hydrolysis

15
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What are the advantages of base hydrolysis?

Reaction goes to completion due to neutralisation by base - more product in the mixture than acid catalysed hydrolysis.

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