Alkanes Flashcards
Define alkanes
Saturated hydrocarbons — contain only C—C and C—H single bonds
How do alkanes react?
Relatively unreactive. Have strong C—C and C—H bonds.
Do not react with acids, bases, oxidising agents, and reducing agents.
They do burn and will react with halogens under suitable conditions.
Describe solubility of alkanes
Insoluble in water.
This is because water molecules are held together by hydrogen bonds which are much stronger than the VDWs forces that act between alkane molecules.
However, alkanes do mix with other relatively non-polar liquids.
Describe polarity of alkanes
Almost non-polar because the electronegativities of carbon and hydrogen are so similar. As a result, the only intermolecular forces between their molecules are weak VDWs forces, and the larger the molecule, the stronger the VDWs forces.
Why does boiling point of alkanes increase as chain length increases?
Because of increasing intermolecular forces (which increases the VDWs forces)
Why do alkanes with branched chains have lower melting points than straight chain alkanes with the same number of carbon atoms?
Because they cannot pack together as closely as unbranched chains and so the VDWs forces are not so effective
Why is crude oil called a fossil fuel?
Because it was formed millions of years ago by the breakdown of plant and animal remains at the high pressures and temperatures deep below the Earth’s surface. Because it forms very slowly, it is effectively non-renewable
What is crude oil a mixture mostly of?
Alkanes (both unbranched and branched)
Where the small amount of other compounds (not alkanes) that is dissolved in crude oil come from? Give an example of one and its effect.
Other elements in the original plants and animals the oil was formed from.
E.g. some contain sulphur. These produce sulphur dioxide when they’re burnt. This can react with oxygen high in the atmosphere to form sulphur trioxide. This reacts with water in the atmosphere to form sulphuric acid.
Process of fractional distillation
The crude oil is first heated in a furnace.
A mixture of liquid and vapour passes into a tower that is cooler at the top than at the bottom.
The vapours pass up the tower via a series of trays containing bubble caps until they arrive at a tray that is sufficiently cool. Then they condense to liquid.
The mixture of liquids that condenses on each tray is piped off.
During fractional distillation, why do the shorter chain hydrocarbons condense in the trays nearer to the top of the tower (where it is cooler)?
Because they have lower boiling points (due to smaller chain length + weaker VDWs forces)
Order of fuels that condense from top to bottom during fractional distillation
Gases Petrol Naphtha Kerosene Gas oil Fuel oil and wax
Are covalent bonds within molecules broken during fractional distillation?
No because it is a physical process.
It is the VDWs forces between the molecules that are broken during vaporisation and reform on condensing.
What is fractional distillation and how is it different from distillation?
Fractional distillation separates a mixture into several components with different ranges of boiling temperatures whereas distillation simply separates all the volatile components of a mixture from the non-volatile ones
Gave the names of two gases produced in fractional distillation.
Methane, ethane, propane, butane etc.
Why are many long chain hydrocarbons cracked?
Because shorter chain products are more economically more valuable than the longer chain material. To meet the demand for the shorter chain hydrocarbons, many of the longer chain fractions are broken into shorter lengths
Why are harsh conditions required to break down alkanes?
Because they’re very unreactive
Name 2 types of cracking
Thermal cracking, catalytic cracking
Describe the conditions required for thermal cracking
High temperatures (700-1200K), high pressure (up to 7000kPa)
How do C—C bonds break during thermal cracking (initially)?
In such a way that one electron from the pair in the covalent bond goes to each carbon atom. So initially two shorter chains are produced, each ending in a carbon atom with an unpaired electron (free radical).
What does thermal cracking tend to produce a high proportion of?
A high proportion of alkenes
What does thermal cracking produce?
An alkane and an alkene
What is done to avoid too much decomposition of alkanes during thermal cracking?
The alkanes are kept in the essential conditions for a very short time, typically one second
What conditions are required for catalytic cracking?
Lower temperatures (~720K), lower pressure (but more than atmospheric), a zeolite catalyst (consisting of silicon dioxide and aluminium oxide)
Give two features of zeolite catalysts
Have a honeycomb structure with an enormous surface area, acidic