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Vocabulary flashcards covering core definitions, organic nomenclature rules, isomerism, fuel processes, mechanisms, and reactions from the Introductory Organic Chemistry and Alkanes lecture notes.
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Hazard
A substance or procedure that has the potential to do harm.
Risk
The probability or chance that harm will result from the use of a hazardous substance or a procedure.
Hydrocarbon
A compound consisting of hydrogen and carbon only.
Saturated Hydrocarbon
A hydrocarbon containing single carbon-carbon bonds only.
Unsaturated Hydrocarbon
A hydrocarbon containing a C=C double bond.
Molecular Formula
The formula which shows the actual number of each type of atom in a compound.
Empirical Formula
Shows the simplest whole number ratio of atoms of each element in the compound.
General Formula
Algebraic formula for a homologous series (e.g. CnH2n).
Structural Formula
Shows the minimal detail that shows the arrangement of atoms in a molecule (e.g. for butane: CH3CH2CH2CH3 or CH3(CH2)2CH3).
Displayed Formula
Shows all the covalent bonds present in a molecule.
Skeletal Formula
Shows the simplified organic formula, shown by removing hydrogen atoms from alkyl chains, leaving just a carbon skeleton and associated functional groups.
Homologous Series
Families of organic compounds with the same functional group and same general formula.
Functional Group
An atom or group of atoms which when present in different molecules causes them to have similar chemical properties.
Homolytic Fission
The breaking of a covalent bond where each atom gets one electron from the bond, forming two free radicals.
Heterolytic Fission
The breaking of a covalent bond where one atom gets both electrons, producing ions.
Free Radical
A reactive species which possesses an unpaired electron.
Mechanism
The detailed step-by-step description of how a chemical reaction proceeds.
Structural Isomers
Compounds with the same molecular formula but different structures (or structural formulae).
Chain Isomers
Compounds with the same molecular formula but different structures of the carbon skeleton.
Position Isomers
Compounds with the same molecular formula but different structures due to different positions of the same functional group on the same carbon skeleton.
Functional Group Isomers
Compounds with the same molecular formula but with atoms arranged to give different functional groups.
Petroleum Fraction
A mixture of hydrocarbons with a similar chain length and boiling point range.
Cracking
Conversion of large hydrocarbons to smaller molecules by breakage of C−C bonds.
Reforming
Process that turns straight chain alkanes into branched and cyclic alkanes and aromatic hydrocarbons.
Fuel
A substance that releases heat energy when burnt.
Complete Combustion
Combustion of alkanes in excess oxygen, producing CO2 and H2O.
Incomplete Combustion
Combustion occurring in a limited amount of oxygen, producing CO (very toxic) and/or C (soot) alongside H2O.
Catalytic Converters
Devices in vehicle exhausts with a ceramic honeycomb coated with catalyst metals (Platinum, Palladium, Rhodium) that turn CO, NO, and unburned hydrocarbons into CO2, N2, and H2O.
Biofuels
Renewable plant-based fuels developed from renewable resources, such as alcohols (e.g. ethanol) and biodiesel.
Initiation
The initial step in a free radical substitution reaction where UV light provides energy to break a bond (e.g. Cl−Cl) by homolytic fission to form free radicals.
Propagation
Steps in a free radical substitution reaction where a free radical reacts with a molecule to form a product and a new free radical, maintaining the chain reaction.
Termination
The final step in a free radical substitution reaction where two free radicals collide and combine to form a stable molecule, ending the chain reaction.