Separate Chemistry 2 Flashcards
Alkanes
Alkanes are a group of saturated hydrocarbons.
The term saturated means that they only have single carbon-carbon bonds, there are no double bonds.
The general formula of the alkanes is CnH2n+2.
They are colourless compounds which have a gradual change in their physical properties as the number of carbon atoms in the chain increases.
Alkanes are generally unreactive compounds but they do undergo combustion reactions, can be cracked into smaller molecules and can react with halogens in the presence of light.
Methane is an alkane and is the major component of natural gas.
Examples of alkanes
methane, ethane, propane, butane, pentane, hexane, heptane, octane, nonane, decane.
Alkenes
Alkenes are a homologous series of hydrocarbons. They’re more reactive than alkanes. All alkenes contain the functional group C=C, a double covalent bond between two of the carbon atoms in their chain.
Alkenes are known as unsaturated because they contain a C=C double bond. This can open up to become a single bond, allowing the two carbon atoms to bond with other atoms.
Examples of alkenes
ethene, propene, butene, pentene, hexene, heptene, octene, nonene, decene, and undecene.
Bromine and alkenes
Alkenes undergo addition reactions in which atoms of a simple molecule add across the C=C double bond.
The reaction between bromine and ethene is an example of an addition reaction.
The same process works for any halogen and any alkene in which the halogen atoms always add to the carbon atoms across the C=C double bond.
Distinguishing between alkanes and alkenes
Halogens can be used to test if a molecule is unsaturated (i.e. contains a double bond).
Br2(aq) is an orange-yellow solution, called bromine water.
The unknown compound is shaken with the bromine water.
If the compound is unsaturated, an addition reaction will take place and the coloured solution will become clear.
Combustion of alkanes
Alkanes and alkenes undergo combustion in the presence of air
Complete combustion occurs to form water and carbon dioxide gas
Hydrocarbon + oxygen ——- carbon dioxide + water
Gasoline is largely composed of isomers of octane, C8H18 , which requires large amounts of oxygen to combust fully.
The efficiency of car engines does not usually enable all the gasoline to burn, so car exhaust will contain small amounts of unburnt hydrocarbons as well as other products such as carbon monoxide and soot which lead to environmental problems.
The carbon dioxide produced is a major contributor to global warming and the replacement of combustion engines with electric vehicles is a major on-going challenge for all countries.
Combustion of alkenes
These compounds undergo complete and incomplete combustion, but because of the higher carbon to hydrogen ratio they tend to undergo incomplete combustion, producing a smoky flame in air.
Polymers
Polymers are large molecules of high relative molecular mass and are made by linking together large numbers of smaller molecules called monomers.
Each monomer is a repeat unit and is connected to the adjacent units via covalent bonds.
Polymerisation reactions usually require high pressures and the use of a catalyst.
Many everyday materials such as resins, plastics, polystyrene cups, nylon etc. are polymers.
These are manufactured and are called synthetic polymers.
Nature also produces polymers which are called natural or biological polymers.
Formation of poly(ethene)
Addition polymers are formed by the joining up of many monomers and only occurs in monomers that contain C=C bonds.
One of the bonds in each C=C bond breaks and forms a bond with the adjacent monomer with the polymer being formed containing single bonds only.
Many polymers can be made by the addition of alkene monomers
Poly(ethene) is formed by the addition polymerisation of ethene monomers and is most commonly called polythene.
Other addition polymers
Other addition polymers are made from alkene monomers with different atoms attached to the monomer such as chlorine, fluorine or a methyl group.
The name of the polymer is deduced by putting the name of the monomer in brackets and adding poly- as the prefix.
For example if propene is the alkene monomer used, then the name is poly(propene).
Deducing the monomer from the polymer
Polymer molecules are very large compared with most other molecule.
Repeat units are used when displaying the formula.
To draw a repeat unit, change the double bond in the monomer to a single bond in the repeat unit.
Add a bond to each end of the repeat unit.
The bonds on either side of the polymer must extend outside the brackets (these are called extension or continuation bonds).
A small subscript n is written on the bottom right hand side to indicate a large number of repeat units.
Deducing the monomer from the polymer
Identify the repeating unit in the polymer.
Change the single bond in the repeat unit to a double bond in the monomer.
Remove the bond from each end of the repeat unit and the subscript n (which can be placed in front of the monomer).
Use of poly(ethene)
Properties - Flexible, cheap and electrically insulating..
Use - Plastic Bags (Low density polythene).
Plastic Bottles (high density polythene).
Use of poly(propene)
Properties - Flexible and strong.
Use - Food Packaging
Ropes
Carpets
Use of poly(chloroethene) (PVC)
Properties - Long-lasting, tough and cheap.
Use - Plastic Sheets
Artificial Leather
Drainpipes and Gutters
Insulation on Wires
Use of poly(tetrafluoroethene) (PTFE)
Properties - Very tough, non-stick and resistant to high temperatures.
Use - Cookware (non stick pans)
Pipework
Condensation polymers
Condensation polymers are formed when two different monomers are linked together with the removal of a small molecule, usually water.
The monomers have two functional groups present, one on each end.
The functional groups at the ends of one monomer react with the functional group on the end of the other monomer, in so doing creating long chains of alternating monomers, forming the polymer.
Polyesters are formed from two different monomers and produce water.
For every ester linkage formed in condensation polymerisation, one molecule of water is formed from the combination of a -H and an -OH group.
Condensation polymer vs addition polymer
Addition polymerisation forms the polymer molecule only.
Condensation polymerisation forms the polymer molecule and one water molecule per linkage.
Polyester
Dicarboxylic acid monomers can react with diol monomers to form ester links this is a condensation reaction. The dicarboxylic acid monomers contain two carboxylic acid groups (-COOH) and the diol monomers contain two alcohol groups (-OH).
The molecule with the ester link has a functional group at each end. These can then react in condensation reactions, making the chain longer. The series of reactions together is known as condensation polymerisation and the resultant polymer is called a polyester.
Problems with polymers
Polymers are formed by the joining up of many small molecules with strong covalent bonds.
This makes polymers unreactive and chemically inert so they don’t easily biodegrade.
Disposing polymers landfill sites
Waste polymers are disposed of in landfill sites but this takes up valuable land, as polymers are non-biodegradable so micro-organisms such as decomposers cannot break them down.
This causes sites to quickly fill up.
Disposing polymers incineration
Polymers release a lot of heat energy when they burn and produces carbon dioxide which is a greenhouse gas that contributes to climate change.
Polymers that contain chlorine such as PVC release toxic hydrogen chloride gas when burned.
If incinerated by incomplete combustion, carbon monoxide will be produced which is a toxic gas.
Disposing polymers recycling
Polymers can be recycled but different polymers must be separated from each other.
This process is difficult and expensive.