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75 Cards in this Set

  • Front
  • Back
Hydrocarbons
organic compounds that contain hydrogen and carbon only
Saturated hydrocarbons
hydrocarbon with single bonds only
unsaturated hydrocarbons
hydrocarbons containing carbon to carbon multiple bonds
aliphatic hydrocarbons
hydrocarbons with carbon atoms joined together in straight or branched chains
alicyclic hydrocarbons
hydrocarbons with carbon atoms joined together in a ring structure
functional group
part of the organic molecule responsible for its chemical reactions
homologous series
series of organic compounds with the same functional group but with each successive member differing by CH2
alkanes
homologous series with the general formula C_NH_2N+2
nomenclature
system of naming compounds
alkyl group
alkane with a hydrogen atom removed, e.g CH_3 or C_2H_5. alkyl groups are often shown as R
general formula
the simplest algebraic formula of a member of a homologous series. e.g general formula of alkanes is C_NH_2N+2
displayed formula
shows the relative positioning of all the atoms in a molecule and the bonds between them
structural formula
shows the minimal detail for the arrangement of atoms in a molecule
skeletal formula
simplified organic formula with hydrogen atoms removed from alkyl chains leaving just a carbon skeleton and associated functional groups
structural isomers
molecules with the same molecular formula but with different structural arrangements of atoms
stereoisomers
compounds with the same structural formula but with a different arrangement of the atoms in space
E/Z isomerism
type of stereoisomerism in which different groups attached to each carbon of a C=C bond may be arranged differently in space because of the restricted rotation of the C+C bond
cis-trans isomerism
special type of E/Z isomerism in which there is a non hydrogen group and hydrogen on each C of a C=C double bond. the cis isomer (Z) has the Hatoms on each carbon on the same side; the trans isomer (E) has the hydrogen on each carbon on different sides
homolytic fission
the breaking of a covalent bond with one of the bonded electrons going to each atom forming two radicals
heterolytic fission
the breaking of a covalent bond with both of the bonded electrons going to one of the atoms forming a cation (+) and an anion (-)
radical
a species with an unpaired electron
nucleophile
an atom (or group of atoms) that is attracted to an electron deficient centre or atom where it donates a pair of electrons to form a new covalent bond
electrophile
an atom (or group of atoms) that is attracted to an electron rich centre of atom where it accepts a pair of electrons to form a new covalent bond
addition reaction
a reaction in which a reactant is added to an unsaturated molecule to make a saturated molecule
substitution reaction
a reaction in which an atom or group of atoms is replaced with an atom or group of atoms
elimination reaction
refers to the removal of a molecule from a saturated molecule to make an unsaturated molecule
fractional distillation
the separation of the components in a mixture into fractions which differ in boiling point (and hence chemical composition) by means of distillation, typically using a fractionating column
cracking
refers to the breaking down of long chained hydrocarbons to form a mixture of shorter chained alkanes and alkenes
catalyst
a substance that increases the rate if a chemical reaction without being used up in the process
radical substitution
type of substitution reaction in which a radical replaces a different atom or group of atoms
mechanism
sequence of steps showing the path taken by electrons in a reaction
initiation
the first step in a radical substitution in which the free radicals are generated by UV radiation
propagation
the two repeated steps in radical substitution that builds up the products in a chain reaction
termination
the final step in a radical substitution when two radicals combine to form a molecule
pi bond
the reactive part of a double bond formed above and below the plane of the bonded atoms by sideways overlap of p-orbitals
electrophilic addition
type of addition reaction in which an electrophile is attracted to an electron rich centre or atom where it accepts a pair of electrons to form a new covalent bond
carbocation
organic ion in which a carbon atom has a positive charge
curly arrow
symbol used in reaction mechanisms to show the movement of an electron pair in the breaking or formation of a covalent bond
polymer
long molecular chain built up from monomer units
monomer
a small molecule that combines with many other monomers to form a polymer
addition polymerisation
the process in which unsaturated alkene molecules (monomers) add on to a growing polymer chain one at a time to form a very long saturated molecular chain (addition polymer)
repeat unit
specific arrangement of atoms that occurs in the structure over and over again.
biodegradable materials
a material that is broken down naturally in the environment by living organisms
volatility
the ease that a liquid turns into a gas. volatility increases ad boiling point decreases
reflux
the continual boiling and condensing of a reaction mixture to ensure that the reaction takes place without the contents of the flask boiling dry
esterification
the reaction of on alchohol with a carboxylic acid to produce an ester and water
dehydration
an elimination reaction in which water is removed from a saturated molecule to make an unsaturated molecule
hydrolysis
a reaction with water or aqueous hydroxide ions that breaks a chemical compound into two compounds
nucleophilic substitution
a type of substitution reaction in which a nucleophile is attracted to an electron deficient centre or atom where it donates a pair of electrons to form a new covalent bond
percentage yield
actual moles / theoretical moles * 100
atom economy
desired molecular mass / total molecular mass * 100
limiting reagent
the substance in a chemical reaction that runs out first
molecular ion M+
the positive ion formed in mass spectrometry when a molecule loses an electron
fragmentation
the process in mass spectrometry that causes a positive ion to split into pieces, one of which is a positive fragment ion
enthalpy
the heat content that is stored in a chemical system
exothermic
a reaction in which the enthalpy of the products is smaller than the enthalpy of the reactants, resulting in heat loss to the surroundings
endothermic
a reaction in which the enthalpy og the products is greater than the enthalpy of the reactants, resulting in heat being taken in from the surroundings
enthalpy profile diagram
a diagram for a reaction to compare the enthalpy of the reactants with the enthalpy of the products
activation energy
the minimum energy required to start a reaction by the breaking of bonds
standard conditions
pressure of 1 kPa (1 atm), 298 K (25 deg. cel.) and a concentration of 1 moldm^-3 (for reactions with aqueous solutions)
standard state
the physical state of a substance under the standard conditions of 100 kPa (1atm), 298 K
standard enthalpy change of reaction
the enthalpy change that accompanies a reaction in the molar quantities expressed in a chemical equation under standard conditions, all reactants and products being in their standard state
standard enthalpy of combustion
the enthalpy change that takes place when one mole of a substance completely reacts with oxygen under standard conditions, all reactants and products being in their standard state
standard enthalpy of formation
the enthalpy change that takes place when one mole of a compound is formed from its constituent elements in their standard states under standard conditions. enthalpy change of formation of an element is 0 kJmol^-1
specific heat capacity
the energy required to raise the temperature of 1g of a substance by 1 deg. cel.
bond enthalpy
the enthalpy change that takes place when breaking by homolytic fission 1 mol of a given bond in the molecules of a gaseous species
hess' law
states that, if a reaction can take place by more than 1 route and the initial and final conditions are the same, the total enthalpy change is the same for each route
enthalpy cycle
a diagram showing alternate routes between reactants and products, which allows the indirect determination of an enthalpy change from other known enthalpy changes using hess' law
rate of reaction
the change in concentration of a reactant or product in a given time
boltzmann distribution
the distribution of energies of molecules at a particular temperature, often shown as a graph
le chatelier's principle
states that when a system in dynamic equilibrium is subjected to a change, the position of equilibrium will shift to minimise the change
the greenhouse effect
the process in which the absorption and subsequent emission of infrared radiation by atmospheric gases warms the lower atmosphere and the planet's surface
troposhere
the lowest layer of the earth's atmosphere extending from the earth's surface up to about 7km (above the poles) and to above 20km (above the tropics)
stratosphere
the second layer of the earth's atmosphere, containing the ozone layer, about 10km to 50km above the earth's surface
adsorption
the process that occurs when a gas, liquid or solute is held to the surface of a solid, or more rarely, a liquid