Alkanes and Industrial Processes

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Vocabulary flashcards covering the characteristics, nomenclature, industrial processing, reactions, and environmental impacts of alkanes as discussed in the lecture notes.

Last updated 5:52 AM on 8/5/26
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32 Terms

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Alkanes

Saturated hydrocarbons containing only carbon-carbon and carbon-hydrogen single bonds.

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Saturated

Molecules that contain only single bonds between atoms.

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General Formula (Chain Alkanes)

CnH2n+2\text{C}_n\text{H}_{2n+2}

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Straight Chains

Unbranched alkane chains where the C-C-C\text{C-C-C} angle is 109.5o109.5^\text{o}, meaning the chains are not actually straight.

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Ring Alkanes

Alkanes with the general molecular formula CnH2n\text{C}_n\text{H}_{2n} because the end hydrogen atoms are not required.

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Isomerism

When molecules have the same molecular formula but different arrangements of atoms; the number of possible isomers increases with more carbon atoms.

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Van der Waals Forces

Weak intermolecular forces between almost non-polar alkane molecules that increase in strength relative to molecule size.

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Boiling Point Trend

The boiling points of alkanes increase as chain length increases due to increasing intermolecular forces.

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Crude Oil

A fossil fuel and non-renewable resource that is a mixture mostly of branched and unbranched alkanes.

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Fractional Distillation

An industrial physical process used to separate crude oil into mixtures of hydrocarbons (fractions) with similar chain lengths and boiling points.

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Fractionating Tower

A tower used for distillation that is cooler at the top than the bottom, allowing vapors to condense on trays containing bubble caps.

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Tar (Bitumen)

The thick residue that collects at the base of the fractionating tower used for road surfacing.

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Fracking

Short for hydraulic fracturing; extracting natural gas trapped in shale rock by drilling and forcing pressurized water mixed with sand and chemicals into the rock.

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Cracking

The process of breaking longer, less useful hydrocarbon chains into shorter, more valuable lengths such as petrol and reactive alkenes.

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Thermal Cracking

A reaction at a high temperature (7001200 K700-1200\text{ K}) and high pressure (up to 7000 kPa7000\text{ kPa}) that produces a high proportion of alkenes.

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Free Radicals

Highly reactive fragments ending in a carbon atom with an unpaired electron, formed when a covalent bond breaks homolytically.

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Catalytic Cracking

A process occurring at about 720 K720\text{ K} and lower pressure using a zeolite catalyst to produce branched alkanes, cycloalkanes, and aromatic compounds.

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Zeolite Catalyst

A catalyst consisting of silicon dioxide and aluminium oxide (aluminosilicates\text{aluminosilicates}) with a honeycomb structure and large surface area.

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Aromatic Compounds

Compounds based on the benzene ring (C6H6\text{C}_6\text{H}_6) where electrons are spread around the ring for stability.

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Fuel

Substances that release heat energy when they undergo combustion.

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Incomplete Combustion

Burning of a fuel in a limited supply of oxygen to form poisonous carbon monoxide (CO\text{CO}) or carbon soot.

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Nitrogen Oxides (NOx\text{NO}_x)

Pollutants produced in petrol engines at high temperatures when nitrogen and oxygen combine; they contribute to acid rain and photochemical smog.

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Flue Gas Desulfurisation

The process of removing sulfur dioxide (SO2\text{SO}_2) from power station gases using a slurry of calcium oxide (lime\text{lime}) or calcium carbonate (limestone\text{limestone}).

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Gypsum

Calcium sulfate (CaSO4×2H2O\text{CaSO}_4 \times 2\text{H}_2\text{O}), a byproduct of flue gas desulfurisation used in builders' plaster and plasterboard.

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Catalytic Converter

A ceramic honeycomb coated with platinum and rhodium catalysts in car exhaust systems to reduce carbon monoxide and nitrogen oxide emissions.

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Greenhouse Effect

The trapping of infrared radiation by atmospheric gases like CO2\text{CO}_2, methane, and water vapour, leading to global warming.

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Carbon Neutral

Activities that produce no net carbon dioxide emissions overall.

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Halogenoalkane

A compound formed when an alkane and a halogen react under ultraviolet (UV\text{UV}) radiation through a substitution reaction.

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Initiation

The first stage of free-radical substitution where a halogen molecule absorbs UV light and breaks homolytically into free radicals.

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Propagation

A two-stage chain reaction step where free radicals react with stable molecules to produce new radicals and stable products.

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Termination

The final step where two free radicals react together to form a stable compound, ending the chain reaction.

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Ozone (O3\text{O}_3)

A molecule in the stratosphere that protects Earth from harmful UV rays; it can be destroyed by chlorine free radicals acting as catalysts.