Developing Fuels Flashcards
What is the standard ethalpy change of a reaction?
ΔrH
The enthalpy change that occurs between the no. moles of reactant specified by the equation under standard conditions with all substances in their standard states.
What is the standard enthalpy change of combustion?
ΔcH
The enthalpy change when 1 mole of substance burns completely in oxygen under standard conditions in standard states
What is the standard enthalpy change of formation?
ΔfH
The enthalpy change when 1 mole of a substance is formed from its constituent elements in their standard states unde standard conditions
What is the (standard) enthlpy change of neutralisation?
The enthalpy change when 1 mole of H+ ions react with 1 mole of OH- ions to form 1 mole H2O under standard conditions and in solutions with a concentration of 1moldm-3
Defined per mole of H2O formed
Standard ionic equation is always the same
What are standard conditions?
Pressure: 1 atmoshpere (101kPa/1.01Nm-2)
Temp: 298K
Concs: 1.00moldm-3
State: Whatever state at 298K
Define system
The reactantd + products being measured (inside the reaction vessel)
Deine surroundings
Everything else that’s not the system - outside the reaction vessel
What is thermochemistry?
The study of the energy + heat associated with chemical reactions
What is enthalpy change?
ΔH
The energy transfered to/from the surrondings when the reaction is carried out in an open container
Define enxothermic
A reaction that gives out energy from the system to the surroundings and heats them
Define endothermic
A reaction that takes energy into the system from the surroundings, cooling the surroundings
Why type of process is bond breaking?
Why?
Endothermic as it requires energy
What type of process is bond forming?
Why?
Exothermic as energy is released
What are the main features of an endothermic reaction?
What does an enthalpy profile for one look like?
Bond breaking
ΔH positive
Takes in energy from surroundings
Cools surroundings
What are the main features of an exothermic reaction?
What does an enthalpy profile for one look like?
Bond making
ΔH negative
Gives out energy to surroundings
Heats up surroundings
If the energy released by forming bonds is greater than the energy required to break bonds, what type of reaction occurs?
An exothermic reaction
If the energy released by forming bonds is less than the energy required to break bonds, what type of reaction occurs?
An endothermic reaction
What formula is used to measure enthalpy change?
E = mcΔT
E = energy transfered (KJmol-1)
m = mass (g)
c = specific heat capacity (Jg-1K-1)
ΔT = temp. change (K)
What do experiments to measure enthalpy changes ususally involve?
Transfering energy to/from water
0.880g C7H16 undergoes complete combustion. The energy released is used to heat 250cm3 water, the temp of which increases by 19º. Calculate ΔcH in kJmol-1. Give to 2 sig figs.
Use E=mcΔT to calculate energy transfered to water.
E = 250 x 4.18 x 19 = 19855J
Convert to kJ = 19.855kJ
- *Calculate moles** of C7H16 burnt using n= m/Mr
0. 880/100 = 0.0088mol - *Scale energy released** during experiment to that released for 1mol burnt
19. 855/0.0088 = 2256.25kJmol-1
Write down ΔcH with correct sign, sig figs, units etc.
ΔcH = -2260kJmol-1
What general formula can be used to calculate ΔH of a reaction?
ΔH = Hproducts - Hreactants
What is the specific heat capacity (c) of water?
4.18Jg-1K-1
What is an alkane?
A saturated hydrocarbon
What are the 4 main features of alkanes?
Have the general formula CnHn+2
Have names ending in -ane
Are saturated - all bonds between Cs single
Are aliphatic - don’t contain benzene rings
How are alkanes named?
Name the longest carbon chain
Identify + name any alkyl side chains in alphabetical order
Use di, tri, tetra before the alkyl prefix is the side chains are identical
Show the position of any side chains using the lowest numbers possible
What is crude oil?
A mixture of many hundreds of different hydrocarbons
What is fractional distillation used to do?
Seperate the different hydrocarbons within crude oil
What is structural formula?
A representation of the atoms, bonds, and groups in a molecule
What is skeletal forumla?
A representation of a molecule using lines to represent C-C bonds
What is the name of the shortest alkane?
Methane
What is the issue with using structural/skeletal formulae to represent molecules?
How is this problem solved?
Don’t accurately represent the 3D shapes of molecules
Wedges and dashed/dotted bonds are used
What do dashed/dotted bonds represent in the 3D structure of a molecule?
A bond in the direction behind the plane of the paper
What do wedges represent in the 3D structure of a molecule?
A bond in the direction in front of the plane of the paper
What does aromatic mean?
An organic molecule/hydrocarbon containing 1+ benzene rings
What is a functional group?
A modifier responsible for the characteristic chemical reactions/behaviours of molecules that contain it
What is a homologous series?
Series of compounds in which all members have the same functional group but have different carbon chain lengths
What is a hydrocarbon?
A compound containing only carbon and hydrogen
(May be used to refer to a section of a molecule)
What is a cycloalkane?
A saturated hydrocarbon where the carbon atoms are joined in a ring
What are the 5 main features of a cycloalkane?
Have the general forumla CnH2n
Have names begining with cyclo-
Have names ending in -ane
Are saturated - all bonds betweens Cs are single
Are aliphatic
What is an alkene?
An unsaturated hydrocarbon containing 1+ C=C bonds
What are the 4 main features of alkenes?
Have the general forumla CnH2n
Have names ending in -ene
Are unsaturated - Have 1+ double bonds between C atoms in molecule
Are aliphatic - don’t contain benzene rings
How are alkenes named?
Have names ending in -ene
The number preceeding the -ene indicates the position of the double bond
If there is more than 1 double bond there will be more than 1 number. Di, tri, tetra will be used before the suffix if this is the case
What are the bond angles around the C=C bond?
Why?
All bond angles around C=C bond 120º
Because there are 3 groups of e- around each C atom - 2 single bonds + 1 double bond
These groups repel each other as far as possible
Describe the bonding in an alkene
A C=C bond contains a sigma (σ) bond and a pi (π) bond.
A σ bond is an area of increased e- density between the C atoms. Only contains 1 area of negative charge
A π bond consists of 2 areas of negative charge. One of these is above the line of the atoms and the other is below
Where are σ bonds found?
Where are π bonds found?
σ bonds found in single bonds
π bonds found in double bonds (along with a σ bond)
What is an electrophile?
A positive ion or molecule with a partial positive charge on one of the atoms
This causes it to be attracted to a negatively charged area
It will react by accepting a lone-pair to form a dative covalent bond
What is electrophilic addition?
A reaction in which an electrophile joins onto an alkene/molecule with double/triple bond
No atoms are removed from the alkene/molecule it joins on to
When is a covalent bond said to be polarised?
If the electrons are unevenly distribute between the atoms
What is a carbocation?
A molecule containing a carbon that has a positive charge
It is formed as an intermediate in electrophilic addition
Describe the electrophilic addition reaction between ethene and bromine
- The bromine molecule approaches the alkene + negative electron sink
- This causes the electrons in the bromine molecule are repelled back along the molecule causing the electron density to become unevenly distributed. It is polarised
- The bromine atom nearest the alkene becomes slightly +ively charged and acts as an electrophile
- A pair of e- from the alkene moves towards the Brδ+ and a C-Br bond is formed
- The carbon species is now a carbocation
- The other bromine, now negatively charged, bonds with the carbocation
What is the experimental evidence for the mechanism of electrophilic addition?
If Cl- ions are present when ethene reacts with bromine, the molecule BrCH2CH2Cl forms as well as the expected BrCH2CH2Br
This is because both Cl- and Br- ions can attack the intermediate carbocation
I.e. when other anions present, next anion will always to remaining side not added to
What is the general rule that determines where the anion will add to the alkene?
Anion will always add (first) to the end with the least steric hindrance
i.e. end with least atoms/molecules in the way
What is the product and conditions for when Br2 is used as an electrophile to react with ethene?
CH2BrCH2Br 1,2-dibromoethane
Room temp + pressure
What is the product and conditions for when HBr(aq) is used as an electrophile to react with ethene?
CH3CH2Br bromoethane
Aqueous solution, room temp + pressure
What is the product and conditions for when H2O is used as an electrophile to react with ethene?
(Hydration)
CH3CH2OH ethanol
Phosphoric acid adsorbed onto silica catalyst, 300ºC + 60atm
If conc H2SO4 used then at 1atm + steam used
What is the product and conditions for when H2 is used as an electrophile to react with ethene?
(Hydrogenation)
CH3CH3 ethane
If Pt catalyst, room temp + pressure
If Ni catalyst, 150ºC + 5atm
What is a monomer?
A molecule which is the starting material for a polymer
Is unsaturated
What is a polymer?
A long-chain molecule formed when lots of small, repeating units called monomers join together
They are saturated
What can be used to test for unsaturation?
Bromine - is decolorised if unsaturated.
Goes from brown to colourless
How can bromine be used to test for unsaturation?
In the presence of unsaturation, changes from orange to colourless
What 2 general types of alkene monomer can addition polymers be made from?
One type of alkene monomer
-A-A-A-A-A-A-
More than one type of alkene monomer (used in copolymerisation)
-A-B-A-B-A-B-