1/31
Vocabulary flashcards covering the characteristics, nomenclature, industrial processing, reactions, and environmental impacts of alkanes as discussed in the lecture notes.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
Alkanes
Saturated hydrocarbons containing only carbon-carbon and carbon-hydrogen single bonds.
Saturated
Molecules that contain only single bonds between atoms.
General Formula (Chain Alkanes)
CnH2n+2
Straight Chains
Unbranched alkane chains where the C-C-C angle is 109.5o, meaning the chains are not actually straight.
Ring Alkanes
Alkanes with the general molecular formula CnH2n because the end hydrogen atoms are not required.
Isomerism
When molecules have the same molecular formula but different arrangements of atoms; the number of possible isomers increases with more carbon atoms.
Van der Waals Forces
Weak intermolecular forces between almost non-polar alkane molecules that increase in strength relative to molecule size.
Boiling Point Trend
The boiling points of alkanes increase as chain length increases due to increasing intermolecular forces.
Crude Oil
A fossil fuel and non-renewable resource that is a mixture mostly of branched and unbranched alkanes.
Fractional Distillation
An industrial physical process used to separate crude oil into mixtures of hydrocarbons (fractions) with similar chain lengths and boiling points.
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.
Tar (Bitumen)
The thick residue that collects at the base of the fractionating tower used for road surfacing.
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.
Cracking
The process of breaking longer, less useful hydrocarbon chains into shorter, more valuable lengths such as petrol and reactive alkenes.
Thermal Cracking
A reaction at a high temperature (700−1200 K) and high pressure (up to 7000 kPa) that produces a high proportion of alkenes.
Free Radicals
Highly reactive fragments ending in a carbon atom with an unpaired electron, formed when a covalent bond breaks homolytically.
Catalytic Cracking
A process occurring at about 720 K and lower pressure using a zeolite catalyst to produce branched alkanes, cycloalkanes, and aromatic compounds.
Zeolite Catalyst
A catalyst consisting of silicon dioxide and aluminium oxide (aluminosilicates) with a honeycomb structure and large surface area.
Aromatic Compounds
Compounds based on the benzene ring (C6H6) where electrons are spread around the ring for stability.
Fuel
Substances that release heat energy when they undergo combustion.
Incomplete Combustion
Burning of a fuel in a limited supply of oxygen to form poisonous carbon monoxide (CO) or carbon soot.
Nitrogen Oxides (NOx)
Pollutants produced in petrol engines at high temperatures when nitrogen and oxygen combine; they contribute to acid rain and photochemical smog.
Flue Gas Desulfurisation
The process of removing sulfur dioxide (SO2) from power station gases using a slurry of calcium oxide (lime) or calcium carbonate (limestone).
Gypsum
Calcium sulfate (CaSO4×2H2O), a byproduct of flue gas desulfurisation used in builders' plaster and plasterboard.
Catalytic Converter
A ceramic honeycomb coated with platinum and rhodium catalysts in car exhaust systems to reduce carbon monoxide and nitrogen oxide emissions.
Greenhouse Effect
The trapping of infrared radiation by atmospheric gases like CO2, methane, and water vapour, leading to global warming.
Carbon Neutral
Activities that produce no net carbon dioxide emissions overall.
Halogenoalkane
A compound formed when an alkane and a halogen react under ultraviolet (UV) radiation through a substitution reaction.
Initiation
The first stage of free-radical substitution where a halogen molecule absorbs UV light and breaks homolytically into free radicals.
Propagation
A two-stage chain reaction step where free radicals react with stable molecules to produce new radicals and stable products.
Termination
The final step where two free radicals react together to form a stable compound, ending the chain reaction.
Ozone (O3)
A molecule in the stratosphere that protects Earth from harmful UV rays; it can be destroyed by chlorine free radicals acting as catalysts.