They have at least one carbon-carbon double bond, making them unsaturated because they contain two fewer hydrogen atoms than the alkane with the same number of carbon atoms
The first 4 alkenes are ethene, propene, butene, and pentene
Reactions of alkenes:
Alkenes have the functional group C=C
They react with oxygen in combustion reactions, burning in air with smoky flames due to incomplete combustion
Alkenes react with hydrogen, water, and halogens by adding atoms across the carbon-carbon double bond to form a single bond
In each reaction with hydrogen, water, and halogens, the C=C bond is broken to form a C-C bond
The compound added splits into two groups added to the different carbons in the C=C bond
Alcohols:
Alcohols contain the functional group -OH
The first 4 members of the series are methanol, ethanol, propanol, and butanol
Reactions of methanol, ethanol, propanol, and butanol:
Alcohols burn in air, producing carbon dioxide and water
They dissolve in water to form a neutral solution with a pH of 7
Alcohols react with sodium to produce hydrogen and a salt
Alcohols react with oxidising agents to form carboxylic acids
Uses of methanol, ethanol, propanol, and butanol:
Methanol is used as a chemical feedstock, in anti-freeze, and to make biodiesel
Ethanol is the main alcohol in alcoholic drinks, used as a solvent and fuel
All 4 alcohols can be used as fuels
Producing ethanol:
Ethanol can be produced by fermentation of sugar with yeast using renewable sources
Conditions for fermentation: about 35°C, anaerobic, and yeast enzyme catalyst
Sugar → ethanol + carbon dioxide
Carboxylic acids:
Ethanoic acid is a member of the carboxylic acids, having the functional group -COOH
The first four members are methanoic acid, ethanoic acid, propanoic acid, and butanoic acid
Reactions of methanoic acid, ethanoic acid, propanoic acid, and butanoic acid:
They dissolve in water to produce acidic solutions with a pH less than 7
They react with metal carbonates to produce carbon dioxide, a salt, and water
React with alcohols in the presence of an acid catalyst to produce esters
Carboxylic acids do not ionise completely in solutions, making them weak acids with a higher pH than solutions of strong acids of the same concentration