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Chemistry Hess's Law

Total questions: 25

Worksheet time: 22mins

Name
Class
Date
1.

The standard enthalpy change for the combustion of graphite is −393.5 kJ/mol and that of diamond is −395.4 kJ/mol.


What is the enthalpy change for the reaction below, in kJ/mol?

C (s, graphite) → C (s, diamond)

a)

−1.9

b)

+1.9

c)

−788.9

d)

+788.9

2.

Calculate the change in Enthalpy of the combustion reaction of liquid Ethanol (C2H5OH). When Ethanol has an enthalpy of -286 kJ/ mol, water is liquid and oxygen and carbon dioxide are in gas state.

a)

-286 kJ/ mol

b)

1366 kJ/mol

c)

-2732 kJ/ mol

d)

-1366 kJ/mol

3.

The standard enthalpy changes of formation of carbon dioxide and of methanoic acid are −394 kJ/mol and −409 kJ/mol respectively. Calculate the enthalpy change for the reaction

H2 (g) + CO2 (g) → HCOOH (l)

a)

−803 kJ/mol

b)

−15 kJ/mol

c)

+803 kJ/mol

d)

+15 kJ/mol

4.
 How many joules of heat are needed to raise the temperature of 10.0 g of aluminum from 22°C to 55°C, if the specific heat of aluminum is 0.90 J/gx°C?    
a)
297 Joules
b)
0.003 Joules
c)
297 J/gx°C
d)
0.003 J/gx°C
5.
The enthalpy change for the reaction
C(s, graphite) + 1⁄2O
2(g) --> CO(g)
cannot be measured directly since some carbon dioxide is always formed in the reaction.
It can be calculated using Hess’s Law and the enthalpy changes of combustion of graphite and of carbon monoxide.
C(s, graphite) + O2(g) --> CO2    ΔH=-394 kJmol–1
CO(g) + 1⁄2O2(g) --> CO2  
ΔH=-283 kJmol–1  
The enthalpy change for the reaction of graphite with oxygen to give carbon monoxide is 
a)
-677 kJmol–1 
b)
+111 kJmol–1 
c)
-111 kJmol–1 
d)
+677 kJmol–1 
6.
The enthalpies of combustion of C(s), H2(g) and C4H9OH(l) (in kJmol-1) are as follows  
C(s) + O
2(g)   ->  CO2(g)  
                                             ∆H=a
H2(g) + ½O2(g)   ->   H2O(l)                                        ∆H=b
C4H9OH(l) + 6O2(g)   ->   4CO2(g) + 5H2O(l)  ∆H=c
What is the enthalpy change for the reaction shown below?
  4C(g) + 5H2(l) + ½O2(g)   ->   C4H9OH(l)
a)
c – 4a – 5b
b)
2a + 10b - c
c)
4a + 5b - c
d)
2a + 5b + c
7.
The standard enthalpy changes of combustion of carbon, hydrogen and methane are shown in the table. 
Which one of the following expressions gives the correct value for the standard enthalpy change of formation of methane in kJ mol–1?
C(s) + 2H2(g) → CH4(g) 
a)
394 + (2 × 286) – 891 
b)
–394 – (2 × 286) + 891 
c)
394 + 286 – 891 
d)
–394 – 286 + 891 
8.
Given the following data: ΔHf[FeO(s)] = –270kJmol–1
ΔHf [Fe2O3(s)] = –820 kJ mol–1
S
elect the expression which gives the enthalpy change, in kJ mol–1, for the reaction:
2FeO(s) + 1⁄2O2(g) → Fe2O3(s) 
a)
(–820 × 1⁄2) + 270 = –140
b)
(+820 × 1⁄2) – 270 = +140
c)
–820 + (270 × 2) = –280 
d)
+820 – (270 × 2) = +280 
9.
C2H4(g) + H2(g)   ->   C2H6(g)  ∆H°=-137 kJ mol-1
Which statement about this information is correct?
a)
The total energy of the bonds broken in the reactants is greater 
than the total energy of the bonds 
formed in the product 
b)
The bonds broken and the bonds made are of the same strength 
c)
The total energy of the bonds broken in the reactants is less than the total energy of the bonds formed in the product 
d)
No conclusion can be made about the sums of the bond enthalpies in the product compared with the reactants 
10.
Use the chart to answer the following question.
Which is correct about energy changes during bond breaking and bond formation? 
a)
A
b)
B
c)
C
d)
D
11.

Using the equations below:


C(s) + O2(g) → CO2(g) ∆H = –390 kJ

Mn(s) + O2(g) → MnO2(s) ∆H = –520 kJ


what is ∆H (in kJ) for the following reaction?


MnO2(s) + C(s) → Mn(s) + CO2(g)

a)

910

b)

130

c)

-130

d)

-910

12.

Using the equations below


Cu(s) + 1/2O2(g) → CuO(s)H = –156 kJ

2Cu(s) + O2(g) → Cu2O(s)H = –170 kJ


what is the value of ∆H (in kJ) for the following reaction?


2CuO(s) → Cu2O(s) + 1/2O2(g)

a)

142

b)

15

c)

-15

d)

-142

13.

Consider the following equations.


Mg(s) + O2(g) → MgO(s)H = –602 kJ

H2(g) + O2(g) → H2O(g)H = –242 kJ


What is the ∆H value (in kJ) for the following reaction?


MgO(s) + H2(g) → Mg(s) + H2O(g)

a)

-844

b)

-360

c)

+360

d)

+844

14.

The following equations show the oxidation of carbon and carbon monoxide to carbon dioxide.


C(s) +O2(g) CO2(g) ΔH = –x kJ mol–1

CO(g) + O2(g) CO2(g) ΔH = –y kJ mol–1


What is the enthalpy change, in kJ mol–1, for the oxidation of carbon to carbon monoxide?


C(s) + O2(g) CO(g)

a)

x + y

b)

-x - y

c)

y - x

d)

x - y

15.

For Hess' Law to be used what must be the same for all of the reactions being studied?

a)

The initial conditions of pressure and temperature.

b)

The final conditions of pressure and temperature.

c)

The initial and the final conditions of pressure and temperature.

d)

The initial and the final conditions of pressure and temperature, and the number of moles of reactants.

16.

Which of the following statements are true for the reaction:


SO2(g) + 1/2O2(g) ↔ SO3(g) ΔH = –92 kJ mol-1


Where ↔ indicates that the reaction can proceed in the forward and the reverse direction.

a)

The forward and reverse reaction both produce 92 kJ of energy.

b)

Oxidising 2 moles of SO2 would produce twice as much energy.

c)

The reverse reaction has an enthalpy of +92 kJ mol-1.

d)

Collecting the SO3 produced in the liquid state would not change the measured enthalpy.

17.

The standard enthalpy change of formation values of two oxides of phosphorus are:


P4(s) + 3O2(g) → P4O6(s) ΔHf = –1600 kJ mol–1

P4(s) + 5O2(g) → P4O10(s) ΔHf = –3000 kJ mol–1


What is the enthalpy change, in kJ mol–1, for the reaction below?


P4O6(s) + 2O2(g) → P4O10(s)

a)

+4600

b)

+1400

c)

–1400

d)

–4600

18.

Standard conditions are defined as...

a)

298K and 1.00 x 105 kPa

b)

273K and 1.00 x 105 kPa

19.

Hess' Law makes use of which principle to calculate the enthalpy change of a reaction?

a)

The law of conservation of energy

b)

The law of conservation of matter

c)

The law that you will always find a lost item in the last place you look for it

d)

Murphy's law

20.

2 CO + O2 --> 2 CO2 (ΔH=-283 kJ)


If the equation was flipped and multiplied by 2 what would it look like?

a)

2 CO + O2 --> 2 CO2

b)

4 CO + 2 O2 --> 4 CO2

c)

4 CO2 -->4 CO + 2 O2

d)

2 CO2 -->2 CO + O2

21.

4 P + 6 Cl2 --> 4 PCl3 (ΔH=-640 kJ)


If the equation was divided by 2 what would the chemical equation look like?

a)

4 P + 6 Cl2 --> 4 PCl3

b)

2 P + 3 Cl2 --> 2 PCl3

c)

4 PCl3 --> 4 P + 6 Cl2

d)

2 PCl3 -->2 P + 3 Cl2

22.

To calculate ΔH what would we have to do to equation (b)


N2 + 2 O2 --> 2 NO2


Using the following 2 equations:

(a) N2 + O2 --> 2 NO (ΔH = 180 kJ)

(b) 2 NO2 --> 2 NO + O2 (ΔH = 112 kJ)

a)

(b) flip it because O2 is on the products (right)

b)

(b) keep it as is, because O2 is on the reactants (left)

c)

(b) multiply by 2 because O2 have a 2 coefficient in front

23.

To calculate ΔH what would we have to do to equation (a)


N2 + 2 O2 --> 2 NO2


Using the following 2 equations:

(a) N2 + O2 --> 2 NO (ΔH = 180 kJ)

(b) 2 NO2 --> 2 NO + O2 (ΔH = 112 kJ)

a)

(A) flip it because O2 and N2 are in the products (right)

b)

(A) keep it as is, because O2 and N2 are in the reactants (left)

c)

(A) multiply by 2 because N2 and O2 have a 2 coefficient in front

24.

To calculate the ΔH of the final equation what must be done to (b)


2NOCl ---> 2 NO + Cl2


Using the following 2 equations:

(a) 2 NO --> N2 + O2 (ΔH = -180.6 kJ)

(b) N2 + O2 + Cl2 --> 2 NOCl (ΔH = 103.4 kJ)

a)

(b) as is because Cl is on the reactant side (left) on the final

b)

(a) flipped because Cl is on the product side (right) in the final

c)

(a) multiplied by 2 because Cl has a coefficient of 2 in front of NO

25.

What would ΔH be if (a) was kept as is and (b) was flipped and multiplied by 2


Pb + PbO2 + 2 H2SO4 --> 2 H2O + 2 PbSO4


Using the following 2 equations:

(a) Pb + PbO2 + 2 SO3 --> 2 PbSO4 (ΔH = -775 kJ)

(b) SO3 + H2O --> H2SO4 (ΔH = -113 kJ)

a)

-549 kJ

b)

-662 kJ

c)

1001 kJ