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Intermediate

Alcohols

4.7.2.3 Alcohols

Aligned to the AQA 8462 specification

Level
Intermediate
Reading time
5 min
Published
2 July 2026
On this page
  1. 1.The Alcohol Functional Group
  2. 2.Reaction with Sodium
  3. 3.Combustion of Alcohols
  4. 4.Dissolving in Water and Oxidation
  5. 5.Uses of Alcohols and Making Ethanol by Fermentation
  6. 6.Common Exam Mistakes

Key takeaways

  • Alcohols contain the –OH functional group; the first four are methanol, ethanol, propanol and butanol, and their names end in -ol.
  • Alcohols react with sodium to give hydrogen gas, burn in air (combustion) releasing energy, dissolve in water to form neutral solutions, and are oxidised by oxidising agents to carboxylic acids.
  • The main uses of the first four alcohols are as fuels and as solvents; ethanol is also the alcohol in alcoholic drinks.
  • Ethanol can be made by fermentation: sugar is broken down by yeast in aqueous conditions with no air (anaerobic), at about 30–40 °C, forming ethanol and carbon dioxide.

The Alcohol Functional Group

(Separate Chemistry only) Alcohols (4.7.2.3) are assessed only in GCSE Chemistry (Triple), not in Combined Science.

Alcohols are a family of organic compounds that all contain the same reactive group: the –OH group (an oxygen atom joined to a hydrogen atom). This is the alcohol functional group, and because every alcohol has it, they all react in similar ways.

The names of alcohols always end in -ol. You need to know the first four members.

NameCarbonsMolecular formulaStructural formula
Methanol1CH₄OCH₃OH
Ethanol2C₂H₆OC₂H₅OH
Propanol3C₃H₈OC₃H₇OH
Butanol4C₄H₁₀OC₄H₉OH

The displayed formula of ethanol shows the –OH group joined to the carbon chain. Every carbon has four bonds; the oxygen sits between a carbon and the final hydrogen.

Ethanol (C₂H₅OH)

    H   H
    |   |
H — C — C — O — H
    |   |
    H   H

Reaction with Sodium

Alcohols react with sodium metal. A piece of sodium added to an alcohol fizzes as hydrogen gas is given off, and the sodium gradually disappears as it reacts.

When an alcohol reacts with sodium, hydrogen gas is produced. You would see the sodium fizzing and moving as bubbles of hydrogen are released.

This is similar to how sodium reacts with water, but the reaction with an alcohol is gentler. The hydrogen given off can be tested with a lit splint, which produces a squeaky pop. You are not expected to write a balanced equation for this reaction, only to describe what happens: fizzing, sodium dissolving, and hydrogen gas released.

Combustion of Alcohols

Alcohols are flammable and burn in air, releasing energy. This is why they are used as fuels. Complete combustion of an alcohol produces carbon dioxide and water, just like a hydrocarbon.

Worked example — write the balanced equation for the complete combustion of ethanol, C₂H₅OH.

Ethanol has 2 carbons (giving 2 CO₂) and 6 hydrogens (giving 3 H₂O):

Now balance oxygen. The right side has oxygen atoms. The left side already has 1 oxygen inside the ethanol, so the O₂ must supply the other 6, which is 3 O₂ molecules:

Check: left has 2 C, 6 H and O; right has 2 C, 6 H and 7 O. Balanced.

When balancing an alcohol's combustion, remember the –OH oxygen counts. The alcohol already contains one oxygen atom, so the O₂ on the left supplies the rest.

Dissolving in Water and Oxidation

Adding to water. The first four alcohols mix completely with water, dissolving to form a solution that is neutral (about pH 7). Unlike acids, alcohols do not turn the solution acidic; the solution has no effect on universal indicator beyond staying green.

Reaction with an oxidising agent. When an alcohol is warmed with an oxidising agent (for example acidified potassium dichromate), it is oxidised to a carboxylic acid. Ethanol is oxidised to ethanoic acid, the acid found in vinegar.

This link matters: it is why an open bottle of wine turns sour over time. Oxygen from the air slowly oxidises the ethanol in the wine into ethanoic acid, giving a vinegary taste. The same oxidation done deliberately with an oxidising agent produces the carboxylic acid in the lab.

ReactionWhat you observe / product
With sodiumfizzing, hydrogen gas released
Combustion in airburns, releasing energy; makes CO₂ and water
Added to waterdissolves to a neutral (pH 7) solution
With an oxidising agentoxidised to a carboxylic acid

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Uses of Alcohols and Making Ethanol by Fermentation

The main uses of the first four alcohols are as fuels and as solvents. Ethanol dissolves many substances that water cannot, so it is used in products such as perfumes and inks, and it is the alcohol present in alcoholic drinks.

Ethanol for drinks is made by fermentation. Yeast contains enzymes that break down sugar (glucose) into ethanol and carbon dioxide.

You must know the conditions for fermentation:

  • aqueous solution (the sugar is dissolved in water),
  • anaerobic conditions, with air (oxygen) kept out, otherwise the ethanol is oxidised to ethanoic acid,
  • a warm temperature of about 30–40 °C, warm enough for the yeast enzymes to work quickly but not so hot that they are denatured.

Fermentation conditions: sugar dissolved in water, with yeast, no oxygen (anaerobic), kept warm at roughly 30–40 °C.

Common Exam Mistakes

1. Forgetting the alcohol's own oxygen when balancing combustion

An alcohol such as C₂H₅OH already contains one oxygen atom. Count it: the O₂ on the left only has to supply the remaining oxygen needed by the CO₂ and water.

2. Saying alcohols are acidic in water

The first four alcohols dissolve to give neutral solutions (about pH 7). They are not acids. It is their oxidation product, the carboxylic acid, that is acidic.

3. Giving the wrong gas from the sodium reaction

Sodium plus an alcohol releases hydrogen gas (which gives a squeaky pop), not oxygen or carbon dioxide.

4. Getting the fermentation conditions wrong

Fermentation needs yeast, an aqueous sugar solution, no air (anaerobic), and a warm temperature of about 30–40 °C. Too hot denatures the enzymes; letting air in oxidises the ethanol to ethanoic acid.

5. Confusing the oxidation product with an aldehyde or hydrocarbon

Oxidising an alcohol with an oxidising agent produces a carboxylic acid (ethanol → ethanoic acid). At GCSE the product you name is the carboxylic acid.

Key terms

Alcohol
An organic compound containing the –OH functional group, with names ending in -ol.
Functional group
The reactive part of a molecule that gives a family its characteristic reactions; for alcohols it is the –OH group.
Fermentation
The process in which yeast breaks down sugar in aqueous, anaerobic conditions to produce ethanol and carbon dioxide.
Oxidation (of an alcohol)
The reaction of an alcohol with an oxidising agent to form a carboxylic acid.
Anaerobic
Taking place without oxygen (air).

Frequently asked questions

Fermentation needs sugar dissolved in water, yeast, no air (anaerobic conditions), and a warm temperature of about 30–40 °C. The yeast breaks the sugar down into ethanol and carbon dioxide.

The first four alcohols are methanol (CH₃OH), ethanol (C₂H₅OH), propanol (C₃H₇OH) and butanol (C₄H₉OH). All contain the –OH functional group and their names end in -ol.

Reacting an alcohol with an oxidising agent produces a carboxylic acid. For example, ethanol is oxidised to ethanoic acid, the acid found in vinegar.

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