90 total
By the end of this topic, you should be able to:
Recall the reactions (reagents and conditions) by which alkanes can be produced:
Describe:
Describe the mechanism of free-radical substitution with reference to the initiation, propagation and termination steps
Suggest how cracking can be used to obtain more useful alkanes and alkenes of lower Mr from heavier crude oil fractions
Understand the general unreactivity of alkanes, including towards polar reagents in terms of the strength of the C–H bonds and their relative lack of polarity
Recognise the environmental consequences of carbon monoxide, oxides of nitrogen and unburnt hydrocarbons arising from the combustion of alkanes in the internal combustion engine and of their catalytic removal
Alkanes are a type of hydrocarbon (compounds containing only carbon and hydrogen atoms). In alkanes, all the carbon atoms are joined together by single covalent bonds. Each carbon atom forms four single bonds arranged in a tetrahedral shape (like a pyramid with a triangular base) with bond angles of about 109.5°.
Alkanes are found naturally in crude oil and natural gas, making them extremely important as fuels and starting materials for the chemical industry.
Alkenes are hydrocarbons that contain at least one carbon-carbon double bond (C=C). We can convert alkenes into alkanes by adding hydrogen gas (H₂) to them. This process is called hydrogenation.
Reagents and Conditions:
The catalyst is finely divided (broken into very small pieces) to increase its surface area, which makes the reaction happen faster.
Example: Butene + Hydrogen → Butane
In this reaction, the double bond in butene breaks, and hydrogen atoms are added to form butane, which only has single bonds.
Real-world application: Hydrogenation is used to make margarine from vegetable oil. Vegetable oil contains many C=C double bonds. When partially hydrogenated, the oil becomes more solid at room temperature, turning into margarine.
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