CHEMISTRY ONLY
Structure and formula of alkenes
C10) ORGANIC REACTIONS
Alkenes | Hydrocarbons with a double carbon-carbon bond. |
Unsaturated | Alkenes are unsaturated because they contain two fewer hydrogen atoms than their alkane counterparts. |
General formula for alkenes | CnH2n |
Reactions of alkenes
Functional group | Alkenes are hydrocarbons in the functional group C=C. | The functional group of an organic compound determined their reactions. |
Alkene reactions | Alkenes react with oxygen in the same way as other hydrocarbons, just with a smoky flame due to incomplete combustion. | Alkenes also react with hydrogen, water and the halogens. The C=C bond allows for the addition of other atoms. |
Alcohols
Functional group | -OH For example: CH3CH2OH | Methanol, ethanol, propanol and butanol are the first four of the homologous series. |
Alcohol reactions | Alcohols react with sodium, air and water. | Alcohols and sodium: bubbling, hydrogen gas given off and salt formed. Alcohols and air: alcohols burn in air releasing carbon dioxide and water. Alcohols and water: alcohols dissolve in water to form a neutral solution. |
Fermentation | Ethanol is produced from fermentation. | When sugar solutions are fermented using yeast, aqueous solutions of ethanol are produced. The conditions needed for this process include a moderate temperature (25 – 50⁰C), water (from sugar solution) and an absence of oxygen. |
Ethanol
Propanol
Butanol
Methanol
Carboxylic acids
Functional group | -COOH For example: CH3COOH | Methanoic acid, ethanoic acid, propanoic acid and butanoic acid are the first four of the homologous series. |
Carboxylic acid reactions | Carboxylic acids react with carbonates, water and alcohols. | Carboxylic acids and carbonates: These acids are neutralised by carbonates |
Carboxylic acids and water: These acids dissolve in water. | ||
Carboxylic acids and alcohols: The acids react with alcohols to form esters. | ||
Strength (HT only) | Carboxylic acids are weak acids | Carboxylic acids only partially ionise in water. An aqueous solution of a weak acid with have a high pH (but still below 7). |
C11) POLYMERS
Addition polymerisation
Polymers | Alkenes are used to make polymers by addition polymerisation. | Many small molecules join together to form polymers (very large molecules). |
Displaying polymers | In addition polymers, the repeating unit has the same atoms as the monomer. | It can be displayed like this: |
Condensation polymerisation (HT only)
Condensation polymerisation | Condensation polymerisation involves monomers with two functional groups | When these types of monomers react they join together and usually lose small molecules, such as water. This is why they are called condensation reactions. |
Amino acids
DNA and naturally occurring polymers
Amino acids have two functional groups in a molecule. They react by condensation polymerisation to produce peptides.
Glycine
DNA | Deoxyribonucleic acid is a large molecule essential for life. DNA gives the genetic instructions to ensure development and functioning of living organisms and viruses. |
DNA structure | Most DNA molecules are two polymer chains made from four different monomers, called nucleotides. They are in the double helix formation. |
Natural polymers | Other naturally occurring polymers include proteins, starch and cellulose and are all important for life. |
Ethene C2H4
Propene C3H6
Butene C4H8
Pentene C5H10