CGP EXAM QUESTIONS: DF Flashcards
10g of calcium carbonate react with excess dilute hydrochloric acid at RTP to produce calcium chloride, water and carbon dioxide: CaCO3(s) + 2HCl(aq) –> CaCl2(s) + H2O(l) + CO2(g)
What volume of carbon dioxide gas is given off?
Mr of CaCO3 = 40.1 + 12.0 + (3 x 16.0) = 100.1
So 10g of calcium carbonate is (100.1/10) = 0.10 mol
From the equation, 1 mol of CaCO3, reacting with excess HCl, will produce 1 mol of CO2, so 0.10 mol of CaCO3 will produce 0.10 mol of CO2
At RTP, 0.10 mol of gas has a volume of 0.10 x 24.0 = 2.4 dm3
4 dm3 of ethane (C2H6) are burned in 20 dm3 of oxygen to produce carbon dioxide and water vapour.
Write a balanced equation for the reaction.
2C2H6 + 7O2 –> 4CO2 + 6H2O
or C2H6 + 3½O2 –> 2CO2 + 3H2O
4 dm3 of ethane (C2H6) are burned in 20 dm3 of oxygen to produce carbon dioxide and water vapour.
What is the total volume (at constant temperature and pressure) of all species present once the reaction is complete?
A) 20 dm3
B) 24 dm3
C) 26 dm3
D) 30 dm3
C) 26 dm3
6dm3 of unreacted O2, 8 dm3 of CO2 and 12 dm3 of H2O
Magnesium carbonate (MgCO3) thermally decomposes to produce magnesium oxide (MgO) and carbon dioxide. What mass of magnesium carbonate is needed to produce 6.00 dm3 of carbon dioxide at RTP?
MgCO3 –> MgO + CO2
1 mole of MgCO3 produces 1 mole of CO2
At RTP, 6.00 dm3 of CO2 = 6.00/24.0 = 0.250 mol
So, 0.250 mol of CO2 is produced by 0.250 mol of MgCO3
Mr of MgCO3 = 84.3 x 0.250 = 21.1g
At what temperature will 1.28g of chlorine gas occupy 98.6 dm3, at a pressure of 175 Pa?
Moles of Cl2 = (1.28/(35.5 x 2)) = 0.0180 mol
Rearranging pV=nRT to find T gives T = (pV)/nR
So, T = (175 x (98.6 x 10-3))/(0.0180 x 8.314) = 115 K
Explain why the bond enthalpy of C=O in ketones is greater than the bond enthalpy of C-O in alcohols
The C=O bond consists of four shared electrons. The C-O bond is only made up of two shared electrons. This means there is a greater electron density between the positive nuclei in the C=O bond, so the nuclei are more strongly attracted to the shared electrons
Hydrogen peroxide has the structure: H-O-O-H
Using values from the table, calculate the overall enthalpy change for the reaction:
H2O2(aq) –> H2O(l) + ½O2(g)
Overall enthalpy change = total energy absorbed - total energy released
= [(2 x 463) + (1 x 146)] - [(2 x 463) + (½ x 498)]
= 1072 - 1175 = 103 kJ mol-1
If the standard enthalpy change of formation of Al2O3(s) is -1676 kJ mol-1 and the standard enthalpy change of formation of MgO(s) is -602 kJ mol-1, calculate the enthalpy change of the following reaction:
Al2O3(s) + 3Mg(s) –> 2Al(s) + 3MgO(s)
ΔrHϴ = sum of ΔfHϴ (products) - sum of ΔfHϴ (reactants)
= [0 + (3 x -602)] - [-1676 + 0]
= 130 kJ mol-1
Write a balanced equation, including state symbols, for the complete combustion of propane gas.
C3H8(g) + 5O2(g) –> 3CO2(g) + 4H2O(l)
Using the values of ΔfHϴ given in the table, draw an enthalpy cycle to determine the standard enthalpy of combustion of propane. Hence, calculate a value for ΔcHϴ [propane]
ΔcHϴ = sum of ΔfHϴ (products) - sum of ΔfHϴ (reactants)
= [(3 x -394.0) + (4 x -285.0)] - [(-104.7) + 0]
= -2221 kJ mol-1
The equation below shows the fermentation of glucose
C6H12O6(s) –> 2C2H5OH(l) + 2CO2(g)
Calculate the enthalpy change for the reaction.
Use the enthalpy cycle and the standard enthalpies of combustion shown below in your calculations
ΔrHϴ = ΔcHϴ (glucose) - 2ΔcHϴ (ethanol)
= [-2820] - [2 x -1367]
= -86 kJ mol-1
The initial temperature of 25.0 cm3 of 1.00 mol dm-3 hydrochloric acid in a polystyrene cup was measured at 19.0 oC. This acid was exactly neutralised by 25.0 cm3 of 1.00 mol dm-3 sodium hydroxide solution.
The maximum temperature of the resulting solution was measure as 25.8oC
Calculate the standard enthalpy change of neutralisation for the reaction. (You many assume the neutral solution formed has a specific heat capacity of 4.18 J g-1 K-1, and a density of 1.00g cm-3.)
Δ*T* = 25.8 - 19.0 = 6.80<sup>o</sup>C = 6.80 K m = 25.0 + 25.0 = 50.0 cm<sup>3</sup> of solution, which has a mass of 50.0g
Assume density to be 1.00g cm-3
Heat produced by reaction = mcΔT
= 50.0 x 4.18 x 6.80 = 1421.2 J
No. of moles of HCl = 1 x (25.0/1000) = 0.0250
No. of moles of NaOH = 1 x (25.0/1000) = 0.0250
Therefore, no. of moles of water = 0.0250
Producing 0.0250 mol of water takes 1421.2 J of heat, therefore producing 1 mol of water takes 1421.2/0.0250 = 56 848 J
= 58.6 kJ
So enthalpy change is -56.8 kJ mol-1 (3.s.f)
negative - because exothermic
A 50.0 cm3 sample of 0.200 mol dm-3 copper(II) sulfate solution placed in a polystyrene beaker gave a temperature increase of 2.00 K when excess zinc powder was added and stirred. (Ignore the increase in volume due to the zinc.)
Calculate the enthalpy change when 1 mol of zinc reacts. Assume the solution’s specific heat capacity is 4.18 J g-1 K-1. The equation for the reaction is: Zn(s) + CuSO4(aq) –> Cu(s) + ZnSO4(aq)
No. of moles of CuSO4 = 0.200 x (50.0/1000) = 0.0100 mol
From the equation, 1 mole of CuSO4 reacts with 1 mole of Zn
So, 0.0100 mol of CuSO4 reacts with 0.0100 mol of Zn
Heat produced by reaction = mcΔT
= 50.0 x 4.18 x 2.00 = 418 J
0.0100 mol of zinc produces 418 J of heat, therefore 1 mol of zinc produces 418/0.0100 = 41800 J = 41.8 kJ
So the enthalpy change is -41.8 kJ
A 50.0 cm3 sample of 0.200 mol dm-3 copper(II) sulfate solution placed in a polystyrene beaker gave a temperature increase of 2.00 K when excess zinc powder was added and stirred. (Ignore the increase in volume due to the zinc.)
The equation for the reaction is: Zn(s) + CuSO4(aq) –> Cu(s) + ZnSO4(aq)
Draw a labelled enthalpy profile diagram for this reaction, showing Ea and ΔrH
The following reaction represents an important stage in the industrial manufacture of sulfuric acid
2SO2(g) + O2(g) –> 2SO3(g)
The catalyst used is V2O5(s). Explain why this is considered a heterogeneous catalyst.
V2O5(s) is classed as a heterogeneous catalyst, as it is in a different state/phase from the reactants
Vanadium(V) oxide’s a solid, but the reactants are gases
The following reaction represents an important stage in the industrial manufacture of sulfuric acid
2SO2(g) + O2(g) –> 2SO3(g)
The catalyst used is V2O5(s). How could you show, experimentally, that V2O5(s) is a catalyst and not a reactant?
Find the mass of the V2O5(s) before and after the reaction - if it is acting as a catalyst, they will be the same
The following reaction represents an important stage in the industrial manufacture of sulfuric acid
2SO2(g) + O2(g) –> 2SO3(g)
The catalyst used is V2O5(s). Platinum catalysts are more efficient than vandium catalysts but are seldom used because they are susceptibel to poisoning by arsenic. Suggest an explanation for how the poisoning happens
The arsenic probably clings to the surface of the platinum and stops it getting involved in the reaction
This is how heterogeneous catalysts are normally poisoned
Crude oil is a source of fuels and petrochemicals. It’s vaporised and separated into fractions using fractional distillation. Some heavier fractions are processed using cracking
Give one economic reason why a catalyst is used in the cracking process
Cracking can be carried out at lower temperatures and pressures using a catalyst
Crude oil is a source of fuels and petrochemicals. It’s vaporised and separated into fractions using fractional distillation. Some heavier fractions are processed using cracking
Write an equation for the thermal cracking of dodecane, C12H26
E.g. C12H26 –> C2H4 + C10H22
Many answers - make sure C’s and H’s balance and there’s an alkane and an alkene
There are a number of different molecules with the molecular formula C5H10
Draw an unbranched cycloalkane with this fomula
There are a number of different molecules with the molecular formula C5H10
Draw a branched alkene with this fomula
There are a number of different molecules with the molecular formula C5H10
Draw an unbranched alkene with this fomula