F. CARBOXYLIC ACIDS
Functional group
• Carboxyl group ( -COOH )
General formula
• CnH2n+1COOH (n=0,1,2,….)
2.6 Analysing carboxylic acid
State the general formula of carboxylic acids | Identify the functional group of carboxylic acids
n Name Molecular Structural Formulae
Formulae
0 Methanoic acid HCOOH
1 Ethanoic acid CH3COOH
2.6 Analysing carboxylic acid
List the names and the molecular formulae of the first four carboxylic acids
n Name Molecular Structural Formulae
Formulae
2 Propanoic acid C2H5COOH
3 Butanoic acid C3H7COOH
2.6 Analysing carboxylic acid
List the names and the molecular formulae of the first four carboxylic acids
Synthesised/making of ethanoic acids
Oxidation of alcohol
C2H5OH+ 2[O] → CH3COOH + H2O
Ethanol Ethanoic acid
• Reflux ethanol with acidified potassium
dichromate(VI) solution or acidified potassium
manganate(VII) solution
2.6 Analysing carboxylic acid
Describe the preparation of ethanoic acid in the laboratory
2.6 Analysing carboxylic acid
Describe the preparation of ethanoic acid in the laboratory
2.6 Analysing carboxylic acid
Describe the preparation of ethanoic acid in the laboratory
2.6 Analysing carboxylic acid
Describe the preparation of ethanoic acid in the laboratory
Solubility Colour
• Simple molecules are • Colourless
very soluble in water liquid
• Due to water molecule Boiling point
being strongly
attracted to the – • High boiling
COOH group point
• Solubility ↓ when Physical Odour
number of carbon per properties of
molecule ↑ • Sharp/unplea
carboxylic sant smell
State acids
• Larger molecules
(C10 above) are
wax-like solids
2.6 Analysing carboxylic acid
State the physical properties of ethanoic acid
Chemical properties
Acid properties
• CH3COOH is a weak monoprotic acid
• Only one hydrogen atom can ionize in water to
produce H+ ion
CH3COOH ↔ CH3COO- + H+
Ethanoic acid Ethanoate ion
• Partially dissociate in water
• Turn moist blue litmus → red
• React slowly with metals, bases and carbonates
2.6 Analysing carboxylic acid
Describe the chemical properties of ethanoic acid
Reaction with metals
Carboxylic acid + metal → salt + H2
2CH3COOH + Zn → Zn(CH3COO)2 + H2
Ethanoic acid Zinc ethanoate
2.6 Analysing carboxylic acid
Describe the chemical properties of ethanoic acid
2.6 Analysing carboxylic acid
Describe the chemical properties of ethanoic acid
Reaction with bases
Carboxylic acid + bases → salt + H2O
CH3COOH + NaOH → CH3COONa + H2O
Ethanoic acid Sodium
ethanoate
2CH3COOH + CuO → Cu(CH3COO) 2 + H2O
Ethanoic acid Copper
ethanoate
2.6 Analysing carboxylic acid
Describe the chemical properties of ethanoic acid
2.6 Analysing carboxylic acid
Describe the chemical properties of ethanoic acid
Reaction with carbonates
Carboxylic acid + carbonates → salt + CO2 + H2O
2CH3COOH + CaCO3 → Ca(CH3COO)2 + CO2 + H2O
Ethanoic acid Calcium
ethanoate
2.6 Analysing carboxylic acid
Describe the chemical properties of ethanoic acid
2.6 Analysing carboxylic acid
Describe the chemical properties of ethanoic acid
Reaction with alcohols
Carboxylic acid + alcohol → ester + H2O
Catalyst: Concentrated H2SO4
CH3COOH + C4H9OH → CH3COOC4H9 + H2O
Ethanoic Butan-1-ol Buthyl ethanoate
acid
2.6 Analysing carboxylic acid
Describe the chemical properties of ethanoic acid
Uses of carboxylic acids
Ethanoic acid
• As a flavouring
• As a preservative
• Used with other chemicals to make drugs, dyes, paints,
insecticides and plastics
Methanoic acid
• Used to coagulate latex
Fatty acids (long-chain carboxylic acids)
• Used in making soaps
Benzoic acid
• Preservative in food
2.6 Analysing carboxylic acid
Explain with examples the uses of carboxylic acids in everyday life