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empirical formula
a formula which shows the simplest whole number ratio of atoms of each element in a commpound
molecular formula
a formula which shows the actual number of atoms of each element in a molecule
molar gas volume
the volume of one mole of gas under specified conditions of temperature and pressure
percentage yield
actual yield/theoretical yield x 100
atom economy
mass of desired product/total mass of products x 100
homologous series
compounds which have the same general formula, similar chemical properties, show a gradation in physical properties and successive members differ by a CH2 unit
functional group
reactive group within a compound
structural isomers
molecules which have the same molecular formula but a different structural formula
geometric isomers
molecules with the same structural formula, but different arrangement of atoms due to the presence of one or more C=C bond
saturated hydrocarbon
contains no C=C or C triple bond C bond.
hydrocarbon
contains hydrogen and carbon only
substitution
replacing one atom or group with a different atom or group
homolytic fission
bond breaking in which one of the shared electrons goes to each atom
heterolytic fission
bond breaking in which both electrons in the shared pair go to a single atom
radical
a particle with an unpaired electron
unsaturated hydrocarbon
contains at least one C=C or C triple bond C bond.
sigma bond
a covalent bond caused by linear overlap of atomic orbitals
pi bond
a covalent bond formed by the sideways overlap of p orbitals
bond length
the distance between the nuclei of two covalently bonded atoms
polymerisation
joining together of many small molecules to form a large molecule
monomers
many small molecules which join together to form a polymer
polymer
a large molecule formed when monomers join together
primary halogenoalkane
a halogenoalkane which has one carbon atom directly bonded to the carbon atom that is bonded to the halogen. (exceptions are halomethanes)
secondary halogenoalkane
a halogenoalkane which has 2 carbon atoms directly bonded to the carbon atom that is bonded to the halogen
tertiary halogenoalkane
a halogenoalkane which has 3 carbon atoms directly bonded to the carbon atom that is bonded to the halogen
reflux
repeated boiling and condensation of a (reaction) mixture
hydrolysis
breaking up molecules by reaction with water
nucleophile
an ion or molecule, with a lone pair of electrons, that attacks regions of low electron density
elimination
a reaction in which a small molecule is removed from a large molecule
electrophile
an ion or molecule that attacks regions of high electron density
hydrogenation
addition of hydrogen molecule across a C=C
primary carbocation
a carbocation which has one carbon atom directly bonded to the positively charged carbon
secondary carbocation
a carbocation which has two carbon atoms directly bonded to the positively charged carbon
tertiary carbocation
a carbocation which has three carbon atoms directly bonded to the positively charged carbon
miscibility
liquids which mix in all proportions ie. form a single layer
primary alcohol
an alcohol which has one carbon atom directly bonded to the carbon atom that is bonded to the -OH group. (Exception is methanol)
secondary alcohol
an alcohol which has two carbon atoms directly bonded to the carbon atom that is bonded to the -OH group
tertiary alcohol
an alcohol which has three carbon atoms directly bonded to the carbon atom that is bonded to the -OH group
ground state
a molecular vibration which is in the lowest possible energy state
wavenumber
the reciprocal of the wavelength and it is measured in cm-1
endothermic
a reaction in which the enthalpy of the products is greater than the enthalpy of the reactants
exothermic
a reaction in which the enthalpy of the products is less than the enthalpy of the reactants
standard conditions
298K and 100kPa
standard enthalpy change
change in heat energy at constant pressure, measured in standard conditions
standard enthalpy of combustion
the enthalpy change when one mole of a substance is completely burnt in oxygen under standard conditions
standard enthalpy of formation
the enthalpy change when one mole of a compound is formed from its elements under standard conditions
standard enthalpy of neutralisation
the enthalpy change when one mole of water is produced in a neutralisation reaction under standard conditions
conservation of energy
energy cannot be created or destroyed but it can change from one form to another
hess's law
the enthalpy change for a reaction is independent of the route taken, provided the initial and final conditions are the same
average bond enthalpy
the energy required to break one mole of a given bond averaged over many compounds
reaction rate
the change of the concentration (amount) of a reactant or product with respect to time
catalyst
a substance which increases the rate of reaction but does not get used up.
activation energy
the minimum amount of energy required for a reaction to occur
reversible
a reaction which goes in both the forward and backward directions
dynamic equilibria
rate of forward reaction is equal to the rate of the backward reaction
equilibrium
a reversible reaction in which the amount of each reactant/product remains constant
homogenous
a reaction in which all the reactants and products are in the same physical state
heterogenous equilibria
a reaction in which all the reactants and products are not in the same state
heterogenous catalyst
the catalyst is in a different phase from the reactants
s-block element
an element which has an atom with highest energy/outer electron in an s-shell orbital
solubility
the maximum mass of solute that will dissolve in 100g of solvent at a stated temperature
Kc
Kc = [C]c[D]d
[A]a[B]b
aA + bB --> cC + dD