The reaction between alkanes and group 7 Elements is called homolytic fission
Hydrocarbons are compounds containing only hydrogens and carbons
Catenation is the ability for carbon to form chains and rings
A homologous series are a family of compounds with the same functional group which differ in formula by CH2 from the next member
A homologous series will
have the same general formula
have similar chemical properties
contain the same functional groups
A functional group is the atom or group of atoms responsible for the chemical behaviour of a molecule
Each functional group has its own distinctive properties which means the properties of a compound is controlled by the functional groups it has
Aromatic compounds are made up of chains of carbon atoms which may be straight or branched
Alicyclic/ cyclic compounds are made up of closed rings of carbon atoms and form cyclo alkanes
Aromatic compounds contain arene (benzene like) rings and often have distinctive smells which aren’t alway pleasant
Saturated compounds contain only single covalent bonds between carbons. They have a maximum number of hydrogens
Unsaturated compounds contain double or triple bonds between carbons atoms which can have more hydrogen atoms added to form additional C-H bonds. They don’t have the maximum number of hydrogens bonded to them
Empirical formula is the simplest whole number ratio of atoms
C5H12
The molecular formula is the actual number of each type of atoms
Structural formula is in minimal detail of how the functional groups and atoms are bonded together
CH3CH2CH3
Displayed formula shows all the atoms and bonds between them in a compound
Skeletal formula shows the functional group but hydrocarbons shown as lines
Writing the names for organic compounds goes in alphabetical order
A structural isomer occurs when two or more compounds have the same molecular formula but different structural formulae
Chain isomers are a type of structural isomer. They have a different arrangement of the carbon chain but the same molecular formula.
The shorter the chain of the alkane the weaker the forces of attraction making them easier to boil
Branching decreases the boiling point because it creates a smaller surface area but increases melting point
Attractive forces between branched molecules are weaker because the branching prevents close contact with other molecules
Alkanes are insoluble
Fractions collected from fractional distillation need further refining to remove sulfur compounds
Cracking a is the break down of long chain molecules to shorter molecules by heating with a catalyst
Straight chain compunds burn less efficiently than branched or cyclic compounds because they have a lower number of bonds to react with oxygen
The process of reforming convert straight chain alkanes into branched alkanes and cyclic compounds making them more efficient for burning
Reforming straight chain alkanes converts them into branched or cyclic compounds through heating and with a platinum catalyst
The greenhouse effect is the trapping of infared radiation in the earths atmosphere which warms the earth
Alkanes burn to produce carbon dioxide and water
Incomplete combustion of alkanes can give then products carbon solid and carbon monoxide
In the presence of ultra violet light alkanes can react with group 7 elements in a substitution reaction. for example it can form chloroalkanes when reacting with chlorine
Steps to a mechanism are
Initiation
propagation
termination
Homolytic fission is the term used to describe the breaking of covalent bonds so that the bonding electrons are shared equally between the atoms involved
Heterolytic fission is when both electrons are converted to one of the atoms involved leaving the remaining atom as an ion
A free radical are molecular fragments or atoms with one unpaired electron and are highly reactive
A substitution reaction Is where one atom or group of atoms replace another atoms or group of atoms
Initiation step goes form 0 free radicals to 2 free radicals as a product
Propagation has 2 parts and has 1 free radical reacting with 1 non free radicals to produce 1 non free radical and 1 free radical