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Vocabulary practice flashcards covering basic organic chemistry, reaction rates, chemical equilibrium, and acid-base theories based on the lecture transcript.
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Homologous series
A series of organic compounds that can be described by the same general formula OR in which one member differs from the next with a CH2 group.
Alkanes
Organic molecules with a carbon-carbon single bond (C−C) structure containing only C−H and C−C single bonds.
Alkenes
Organic molecules containing a carbon-carbon double bond (C=C) functional group.
Alkynes
Organic molecules containing a carbon-carbon triple bond (C=C) functional group.
Haloalkanes
Organic molecules containing a halogen atom (X=F,Cl,Br,I) bonded to a saturated C atom.
Alcohols
Organic molecules containing a hydroxyl group bonded to a saturated C atom.
Aldehydes
Organic molecules containing a formyl group (C−H with a double bond to oxygen on the same carbon).
Ketones
Organic molecules containing a carbonyl group bonded to two C atoms.
Carboxylic acids
Organic molecules containing a carboxyl group functional group.
Esters
Organic molecules containing a functional group with an oxygen atom double bonded to a carbon atom that is also single bonded to another oxygen atom within the chain.
Dipole-dipole forces
Intermolecular forces between two polar molecules.
Induced dipole forces or London forces
Intermolecular forces between non-polar molecules.
Hydrogen bonding
Forces between molecules in which hydrogen is covalently bonded to nitrogen, oxygen or fluorine; a special case of dipole-dipole forces.
Boiling point
The temperature at which the vapour pressure of a substance equals atmospheric pressure.
Melting point
The temperature at which the solid and liquid phases of a substance are at equilibrium.
Vapour pressure
The pressure exerted by a vapour at equilibrium with its liquid in a closed system.
Organic molecules
Molecules containing carbon atoms.
Molecular formula
A chemical formula that indicates the type of atoms and the correct number of each in a molecule.
Structural formula
A compound formula showing which atoms are attached to which; atoms are represented by symbols and lines represent ALL the bonds.
Condensed structural formula
A notation that shows the way in which atoms are bonded together in the molecule but does not show all bond lines.
Hydrocarbon
Organic compounds that consist of hydrogen and carbon only.
Saturated compounds
Compounds in which there are no multiple bonds between C atoms in their hydrocarbon chains.
Unsaturated compounds
Compounds with one or more multiple bonds between C atoms in their hydrocarbon chains.
Functional group
A bond or an atom or a group of atoms that determine(s) the physical and chemical properties of a group of organic compounds.
Structural isomer
Organic molecules with the same molecular formula, but different structural formulae.
Chain isomers
Molecules with the same molecular formula, but different types of chains.
Positional isomers
Molecules with the same molecular formula, but different positions of the side chain, substituents or functional groups on the parent chain.
Functional isomers
Molecules with the same molecular formula, but different functional groups.
Hydrohalogenation
The addition of a hydrogen halide to an alkene.
Halogenation
The reaction of a halogen (Br2,Cl2) with a compound.
Hydration
The addition of water to a compound.
Hydrogenation
The addition of hydrogen to an alkene.
Dehydrohalogenation of haloalkanes
The elimination of hydrogen and a halogen from a haloalkane.
Dehydration of alcohols
The elimination of water from an alcohol.
Cracking of alkanes
The chemical process in which longer chain hydrocarbon molecules are broken down to shorter more useful molecules.
Hydrolysis
The reaction of a compound or salt with water.
Macromolecule
A molecule that consists of a large number of atoms.
Polymer
A large molecule composed of smaller monomer units covalently bonded to each other in a repeating pattern.
Monomer
Small organic molecules that can be covalently bonded to each other in a repeating pattern to form a polymer.
Polymerisation
A chemical reaction in which monomer molecules join to form a polymer.
Addition polymerisation
A reaction in which small molecules join to form very large molecules by adding on double bonds.
Condensation polymerisation
Molecules of two monomers with different functional groups undergo condensation reactions with the loss of small molecules, usually water.
Heat of reaction (ΔH)
The energy absorbed or released in a chemical reaction.
Exothermic reactions
Chemical reactions that release energy (ΔH<0).
Endothermic reactions
Chemical reactions that absorb energy (ΔH>0).
Activation energy
The minimum energy needed for a reaction to take place.
Activated complex
The unstable transition state from reactants to products.
Reaction rate
The change in concentration of reactants or products per unit time.
Catalyst
Substance that increases the rate of a reaction by providing an alternative path of lower activation energy, therefore decreasing the net activation energy.
Chemical equilibrium
A dynamic equilibrium when the rate of the forward reaction equals the rate of the reverse reaction.
Reversible reaction
A reaction where products can be converted back to reactants.
Open system
A system that continuously interacts with its environment, as opposed to a closed system which is isolated.
Arrhenius Acid
A substance that produces hydrogen ions (H+) or hydronium ions (H3O+) when it dissolves in water.
Arrhenius Base
A substance that produces hydroxide ions (OH−) when it dissolves in water.
Lowry-Brønsted Theory Acid
An acid is defined as a proton (H+ ion) donor.
Lowry-Brønsted Theory Base
A base is defined as a proton (H+ ion) acceptor.
Strong acids
Acids that ionise completely in water to form a high concentration of H3O+ ions.
Weak acids
Acids that ionise incompletely in water to form a low concentration of H3O+ ions.
Strong bases
Bases that dissociate completely in water to form a high concentration of OH− ions.
Weak bases
Bases that dissociate or ionise incompletely in water to form a low concentration of OH− ions.
Concentrated acids/bases
Solutions containing a large amount (number of moles) of acid or base in proportion to the volume of water.
Dilute acids/bases
Solutions containing a small amount (number of moles) of acid or base in proportion to the volume of water.
Conjugate acid-base pairs
When the acid, HA, loses a proton, its conjugate base, A−, is formed; when the base, A−, accepts a proton, its conjugate acid, HA, is formed.
Ampholyte
A substance that can act as either an acid or as a base (also called an amphiprotic substance).
Equivalence point of a titration
The point at which the acid/base has completely reacted with the base/acid.
Endpoint of a titration
The point where the indicator changes colour.
Auto-ionisation of water
The reaction of water with itself to form H3O+ ions and OH− ions.