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def. organic chemistry
the study of compounds of carbons
def. fossils duels
fuels that were formed from the remains of dead plants and animals that live
def. homologous series
series of compounds with similar chemical properties a general chemical formula and each successive member differing CH2
The Alkanes
single bonds between carbon atoms
saturated compound
def. saturated compound
a compound where there are only single bonds between its atoms.
alkanes
general formula: CnH2n +2
properties of alkane
soluble in non-polar solvents e.g cyclohexane
insoluble in water because alkanes are non-polar - Van der Waals forces
Larger molecules have stronger Van der Waals forces, increasing their boiling and melting points
def. structural isomer
compounds that have the same molecular formulae but different structural formulae
alkenes
the homologous series has a double bond between two carbon atom
unsaturated compounds
def. unsaturated compounds
a compound which contains one or more double or triple bonds between its atoms
general formula: CnH2n
properties of alkenes
soluble in non polar solvents e.g cyclohexane
insoluble in water because the alkenes are non-polar → Van der Waals forces between molecules
alkynes
series has a triple bond between two carbon atoms
they are unsaturated hydrocarbons
ethyne
general formula of alkyne
CnH2n-2
properties of alkynes
soluble in non-polar solvents e.g cyclohexane
insoluble in water because alkynes are non-polar Van der Waals forces between the molecules
def. aromatic compounds
compounds that contain a benzene ring
e.g Benzene, methylbenzene and ethylbenzene
oil refining
crude oil is made up of a mixture of different hydrocarbons
fractional distillation
used to separate these different hydrocarbons into groups called fractions, based on their boiling points
frational distillation in order (top to bottom)
refiner gases (bottled gas)
gasoline (petrol)
naptha (making chemicals)
kerosene (aircraft fuel)
diesel oil (fuel for cars,lorries,buses)
fuel oil (fuel for ships, power stations)
residue (bitumen for roads and roofs)
def. octane number
a measure of its tendency to resist autoignition
def.autoignition
premature ignition of a fuel-air mixture before a spark is produced
reference hydrocarbons: heptane
octane number: 0
long chain
no branching
reference hydrcarbons: 2,2,4 - trimethylpentane
octane number:100
short chain
branching
factors that affect octane number
length of chain: shorter carbon chains have higher octane number
degree of branching: the more branching, higher octane number
presence of rings: ring structures give a fuel higher octane number
process that raise octane number of a fuel
isomerisation
catakyic cracking
dehydrocylisation
adding oxygenates
isomerisation
involves changing straight chain alkanes into their branched isomers to raise octane number
process of isomerisation
heat in presence of a catalyst
chain breaks
bits rejoin to form a branched compound
catalytic cracking
involves using heat and a catalyst to break down long chain hydrocarbons into short chain molcules
high demand for short chain molecules with high octane numbers
one of the products will always be an alkenedeh
dehydrocyclisation
involves using catalysts to change linear molecules into cyclic molecules and cyclic molecules into aromatic compounds
adding oxygenates
addition of oxygen-containing compunds to raise its octane number - making it burn cleaner - less carbon monoide is formed when its burned
e.g oxygenates: methanol, ethanol, MTBE
hydrogen as a fuel
steam reforming a natural gas: steam is reacted with natural gas using a catalyst
CH4 + H2O → 3H2 + CO
electrolysis of water: an electric current is passed through water
H2O → H2 + 1/2O2
uses of hydrogen
burned as a fuel because it is environmentally friendly - its only waste product is water
note
Hydrogen forms a very explosive mixture with air and is therefore difficult to story and transport without risk of explosion
physical properties of hydrocarbons
boiling points: VAn der Waals occure between hydrocarbons resulting in low boiling points
solubility: only soluble in organic solvents because CH is non polar
e.g cyclohexane
thermochemistry
exothermic reaction
one that produces heat
endothermic
one that absorbs heat
if the heat change is negative
if the heat change is positive
negative - reaction is exothermic - gets hotter
positive - reaction is endothermic - gets cooler
def.heat of reaction
heat change when one mole of a substance is burned completely in excess oxygen
def.heat of combustion
heat of cumbustion is the heat change when one mole of a substance is bruned completely in excess oxygen
combustion equation
fuel + O2 → CO2 + H2O
def. bond energy
the average energy required to break one mole of H+ ions from an acid reacts with one mole of OH- ions from a base
def. heat of neutralisation
heat change when one mole of H+ ions from an acid reacts with one mole of OH- ions from a base
def. Heat of formation
the heat change that takes place in one mole of a compound formed from its element in their standard stae
hess’s law
the sum of the heat changes in the separate stages is equal to the heat change if the reaction is carried out in one stage.