Subjects · Leaving Cert Chemistry
Leaving Cert Chemistry: Functional groups
How often Functional groups comes up on the Chemistry papers, every year it was asked, and questions to try.
HL Asked on 10 of the last 10 Higher Level papers, most recently in 2026. banker
OL Asked on 8 of the last 10 Ordinary Level papers, most recently in 2026. most years
June 2027 is the first exam on the new Chemistry course. These come from the 2016–2026 papers, so read them as a guide.
Quick ones on Functional groups.
- Carbonyl
- Carboxyl
- Hydroxyl
- Ethanol
- Methanoic acid
- Ethanoic acid
- -CHO
- -OH
- -COOH
Show the answers
(a) Carboxyl
(b) Ethanoic acid
(c) -CHO
Higher Level
Asked on 10 of the last 10 Higher Level papers, most recently in 2026. banker
Every paper, year by year
| Year | Where it came up |
|---|---|
| 2026 | Q11(a) |
| 2025 | Q8 |
| 2024 | Q2, Q4(f), Q11(b) |
| 2023 | Q4(i) |
| 2022 | Q8, Q11(b) |
| 2021 | Q4(j), Q8 |
| 2019 | Q2, Q8 |
| 2018 | Q8 |
| 2017 | Q8 |
| 2016 | Q2 |
Links open the State Examinations Commission’s paper for that year.
More Functional groups questions
Functional groups, 3 marks
How does a ketone differ from an aldehyde?
- It has an -OH group joined to a carbon atom instead of a C=O group
- It contains a carbon to carbon double bond next to the C=O group
- Its C=O group is joined to two carbon atoms, not to a hydrogen
Show the answer
Its C=O group is joined to two carbon atoms, not to a hydrogen
Because there is no hydrogen on the carbonyl carbon, ketones are not readily oxidised, unlike aldehydes.
Functional groups, 3 marks
Why is ethanoic acid a much stronger acid than ethanol?
- Ethanoic acid is an ionic compound, so it is already split into ions
- The ethanoate ion is stabilised by resonance, which spreads its negative charge
- Ethanol has more hydrogen atoms, so each one is held more tightly by the molecule
Show the answer
The ethanoate ion is stabilised by resonance, which spreads its negative charge
The charge is shared over both oxygens, so losing H+ is easier. The C=O also pulls electrons from the O-H bond (inductive effect).
Functional groups, 2 marks
Which homologous series has the general formula CnH2n+1OH?
- Alcohols
- Aldehydes
- Carboxylic acids
Show the answer
Alcohols
An alkyl group joined to an -OH group, such as methanol CH3OH and ethanol C2H5OH, fits CnH2n+1OH.
Ordinary Level
Asked on 8 of the last 10 Ordinary Level papers, most recently in 2026. most years
Every paper, year by year
| Year | Where it came up |
|---|---|
| 2026 | Q8 |
| 2025 | Not asked |
| 2024 | Q4(g), Q8 |
| 2023 | Q8 |
| 2022 | Q8 |
| 2021 | Not asked |
| 2019 | Q8 |
| 2018 | Q8 |
| 2017 | Q8 |
| 2016 | Q8 |
Links open the State Examinations Commission’s paper for that year.
More Functional groups questions
Functional groups, 2 marks
Typical smell of an ester?
- Like rotten eggs
- Like vinegar
- Sweet and fruity
Show the answer
Sweet and fruity
Esters are used in flavourings and perfumes. Vinegar smells of ethanoic acid, a carboxylic acid.
Functional groups, 2 marks
Functional group of an ester?
- -CHO
- -COO-
- -OH
Show the answer
-COO-
An ester link joins a carboxylic acid part and an alcohol part. -OH is an alcohol and -CHO an aldehyde.
Functional groups, 2 marks
Carboxylic acid found in ant stings and nettle stings?
- Methanoic acid
- Ethanoic acid
- Benzoic acid
Show the answer
Methanoic acid
Methanoic acid, HCOOH, is the simplest carboxylic acid. Ethanoic acid is in vinegar.
Other Chemistry topics
- Acids and bases
- Atomic structure
- Chemical equilibrium
- Concentration
- Covalent bonding
- Electronegativity
- Fuels and heats of reaction
- Gas laws
- Hydrocarbons
- Mandatory experiments
- Organic reactions
- Oxidation and reduction
- pH
- Rates of reaction
- Shapes of molecules
- The mole
- The periodic table
- Trends
- Volumetric analysis
- Water treatment
- Electron configuration
- Formulas and equations
- Organic synthesis
- Radioactivity
- Instrumentation and separation
- Ionic bonding
- Intermolecular forces
- Electrochemistry
- Environmental chemistry
- Isomerism
- Industrial chemistry
- Lab safety
- States of matter