2020 Chemical Energetics Part 1 Tutorial
2020 Chemical Energetics Part 1 Tutorial
2 [Calorimetry; Hn ]
The chemical reaction between 30 cm3 of 1.0 mol dm3 sodium hydroxide solution
and 20 cm3 of 1.0 mol dm3 sulfuric acid solution in a plastic cup gave rise to a
temperature rise of 7.3 C. The efficiency of the process was expected to be 90 %.
(a) Explain, with the aid of a chemical equation, what is meant by the standard
enthalpy change of neutralisation.
(b) Calculate the standard enthalpy change of the neutralisation reaction.
[Assume specific heat capacity of the solution to be 4.18 J g 1 K1 and its
density to be 1 g cm3.]
(a) Using appropriate data from the Data Booklet, construct a BornHaber cycle
for lithium chloride to determine the lattice energy of lithium chloride.
(b) Explain how you would expect the numerical value of the lattice energy of
sodium chloride to compare with that of lithium chloride.
A 25200 J B 56000 J
C 89600 J D 143000 J
7 The enthalpy change of formation of H2S(g) and H2O(l) are −21 kJ mol1 and
−286 kJ mol1 respectively, and the enthalpy change of vaporisation of water is
+41 kJ mol1.
What is the enthalpy change of reaction for the following process?
H2S(g) + ½O2(g) H2O(g) + S(s)
A –x–y B x+y
C –x+y D x–y
9 The enthalpy change of reaction between zinc and hydrochloric acid can be
measured in the laboratory.
Zn(s) + 2HCl(aq) ZnCl2(aq) + H2(g)
What information, other than that obtained in this experiment, is needed to
calculate a value for the enthalpy change of formation of aqueous ZnCl2?
11 Which statement helps to explain why magnesium and oxygen form MgO instead
of Mg2O?
A Less energy is required to remove one electron from the magnesium atom
than to remove two electrons.
B When Mg2O is formed from its elements, more energy is released than
when MgO is formed.
C The lattice energy of MgO is more exothermic than that of Mg 2O.
D More energy is released in forming the oxide ions from oxygen molecules in
the formation of MgO than in the formation of Mg2O.
12 Table 2 shows the enthalpy change of neutralisation, Hneut, for various acids and
bases.
Table 2
acid base Hneut /kJ mol1
HCl NaOH –57.0
P NaOH –54.0
HCl Q –52.0
H2SO4 R –57.0
Which identifications of P, Q and R are correct?
P Q R
1 CH3COOH NH3 KOH
2 CH3COOH NH3 Ba(OH)2
3 H2SO4 Ba(OH)2 NH3
A 1 only
B 3 only
C 1 and 2 only
D 1, 2 and 3
∆H = –134 kJ mol1
R S
∆H = +92 kJ mol1
∆H = –75 kJ mol1
T U
A 1, 2 and 3
B 1 and 2 only
C 2 and 3 only
D 1 only
14 Which enthalpy changes are required to determine the lattice energy of caesium
hydride, CsH, via the BornHaber cycle?
1 H(g) + e– H–(g)
2 H2(g) 2H(g)
3 Cs(s) Cs+(g) + e–
A 1, 2 and 3
B 1 and 2 only
C 2 and 3 only
D 1 only
(a) Use the data given to calculate the standard enthalpy change for the
reaction. Assume the heat capacity of all solutions = 4.2 J K –1 cm–3 and
concentrations of HCl(aq) and NaHCO3(aq) are both 1.0 mol dm3.
(b) (i) Use the data in Table 3 to calculate another value for standard
enthalpy change for the above reaction.
Table 3
species ∆Hf / kJ mol–1
H2O(l) –285.8
CO2(g) –393.5
HCO3–(aq) –692
H+(aq) 0.0
(ii) Suggest one possible reason why your answers in (a) is different from
that in (b)(i).
2020 JPJC JC1 H2 Chemistry (9729) 6 Topic 5: Chemical Energetics (Part 1)
*18 [∆Hn; Temperature-Correction Curve]
An experiment is performed to find the enthalpy change of neutralisation for the
reaction between aqueous sodium hydroxide and aqueous ethanoic acid.
The temperature of a 40 cm3 solution of 2.0 mol dm3 aqueous sodium hydroxide
in a polystyrene cup is measured every 30 seconds for 1.5 minutes. At the second
minute, a 20 cm3 solution of 2.0 mol dm3 aqueous ethanoic acid is poured into
the aqueous sodium hydroxide. The temperature of the resulting mixture is then
measured every 30 seconds for a further 5 minutes.
temperature / C
time / min
Fig. 1
(i) Suggest a reason for the discrepancy between the ∆Hc for octane you
calculated in (b)(ii) and that given Table 4.
(ii) Suggest what the regular increase in the values of ∆Hc in Table 4
represents.
(iii) The enthalpy change of combustion of ethanol is –1367 kJ mol1, and
the densities of ethanol and octane are 0.79 g cm 3 and 0.70 g cm3
respectively.
Calculate the heat produced by the complete combustion of 1.0 dm 3 of
each fuel and hence, conclude whether ethanol or octane is a better
fuel.
(a) Using relevant data from the Data Booklet and the data in Table 5, construct
an appropriate energy cycle to calculate the enthalpy change of atomisation
of furan.
(CH)4O(l) 4C(g) + 4H(g) + O(g) Ha((CH)4O)
Table 5
enthalpy change of formation of furan –62 kJ mol1
enthalpy change of atomisation of carbon +717 kJ mol1
Note: Enthalpy change of atomisation of a compound is the heat
absorbed when one mole of the compound in its standard state is
turned into its constituent gaseous atoms.
(b) (i) Using appropriate bond energy values from the Data Booklet alone,
calculate another value for the enthalpy change of the reaction in (a).
(ii) The value calculated using this method differs from that calculated in
(a). By considering the definition of bond energy, suggest one reason
for the difference in enthalpy values.
(b) Given the enthalpy change of formation of MgCl2 (s) is –643 kJ mol1,
comment on the stability of MgCl3 (s) relative to MgCl2 (s).
(c) Even though the lattice energy of MgCl3 (s) is the most exothermic, MgCl3 (s)
is not formed.
By considering the relevant ionisation energies of magnesium, explain why this
is so.
(d) (i) Using relevant data in Table 6 and data in Table 7, construct an energy
cycle to calculate a value for the enthalpy change of solution of
magnesium chloride, MgCl2.
Table 7
enthalpy change of hydration of Mg 2+(g) –1920 kJ mol1
enthalpy change of hydration of Cl(g) –381 kJ mol1
(ii) How would you expect the temperature to change when MgCl2 is
dissolved in water?
Fig. 2
To find the enthalpy change of combustion of ethanol, the heat capacity of the
calorimeter is determined first. This is the amount of heat required to raise the
temperature of the calorimeter by 1 C.
(a) (i) Suggest a property of benzoic acid which allows it to be used to find the
heat capacity of a calorimeter.
(ii) There is no heat lost from the calorimeter because of the controlled
temperature water jacket.
Suggest how the controlled temperature water jacket achieves this.
(i) Suggest why sample 1 produced a lower temperature rise than the
other two samples.
(ii) Suggest what the chemist could have done to ensure no black powder
was produced for samples 2 and 3.
(iii) Calculate the heat capacity of the calorimeter from appropriate data in
Table 8. State its units.
Assume that all the energy released from the combustion process is
converted into heat and none is lost to the surrounding.
(c) Once the heat capacity of the calorimeter is determined, the calorimeter can
be used to find the energy changes of combustion for other substances.
However, the energy change calculated by burning a known mass of
substance in the calorimeter is not a true value for its standard enthalpy
change of combustion, Hc; with a small correction the standard enthalpy
change of combustion can be found.
(d) 1.60 g of ethanol (Mr = 46.0) was completely burnt in the calorimeter and the
rise in temperature was 7.6 C.
Calculate the energy change of combustion, in kJ mol 1,of ethanol.
(e) The bomb calorimeter setup consists mainly of the pool of water and the steel
bomb.
Briefly outline how the specific heat capacity of the steel bomb can be
determined.