Review Quiz Part II

Question 1

Which metal will dissolve in hydrochloric acid?

Fe

For a metal to dissolve in HCl, the standard potential for the reaction must be positive. Because the H+/H2 potential is zero, Eorxn = 0 - Eometal.



Question 2

The standard potential of the cell

Pb(s)|PbSO4(s)|SO42-(aq)||Pb2+(aq)|Pb(s)
is +0.23 V at 25oC. Calculate the equilibrium constant for the reaction of 1 M Pb2+(aq) with 1 M SO42-(aq).

5.9 x 107

logK = nEorxn/0.0592.



Question 3

Consider the following cell:

Ni(s)|Ni2+(aq, 0.200 M)||Cl-(aq, 0.0200 M)|Cl2(g, 0.500 atm)|Pt
If the standard voltage for this cell is 1.59 V at 25oC, calculate the voltage of this cell.

+1.70 V

E = Eo - (0.0592/2)log([Cl-]2[Ni2+]/P Cl2)



Question 4

Consider the following cell:

Ag(s)|Ag+(aq, 0.100 M)||Ag+(aq, 1.00 M)|Ag(s)
What is the voltage of this cell?

+0.0592 V

The equation is (anode on left, cathode on right in cell diagram)
Ag+(1.00 M) ----> Ag+(0.100 M) and n = 1.
In this case Eo = 0. Finally, use the Nernst equation.



Question 5

Consider the following cell:

Zn(s)|Zn2+(aq, 0.200 M)||H+(aq, ?)|H2(g, 1.00 atm)|Pt
If Ecell = +0.66 V and Eocell = +0.76 V at 25oC, calculate the concentration of H+ in the cathode cell compartment.

9.1 x 10-3 M

The equation for the reaction is
2H+ + Zn ----> H2 + Zn2+
Apply the Nernst equation. Note, because you are taking exponentials, carry all decimal places in your calculation.



Question 6

Consider the following cell:

Pt|H2(g, 1 atm)|H+(aq, ? M)||Ag+(aq, 1.0 M)|Ag(s)
If the voltage of this cell is 1.04 V at 25oC and the standard potential of the Ag+/Ag couple is +0.80 V, calculate the hydrogen ion concentration in the anode compartment.

8.8 x 10-5 M

The equation for the reaction is
Ag+ + 1/2H2 ----> Ag + H+
Apply the Nernst equation.



Question 7

When a lead-acid battery discharges,

sulfuric acid is consumed.

The cell reactions show that sulfuric acid is used up during discharge. See your text.



Question 8

The products of the electrolysis of CuF2(aq) are

Cu(s), O2(g), and H+(aq).

Fluoride is too difficult to oxidize (Eo = +2.87 V) with respect to water (Eo = +1.23 V or +0.81 V at pH 7) and the latter is preferentially oxidized to give oxygen gas and H+ ions.



Question 9

If 612 C of charge is passed through a solution of Cu(NO3)2(aq), calculate the number of moles of copper deposited.

0.00317 mol

mol e- = C/F = 612 C/(96485 C.mol-1) = 6.34 x 10-3 mol e-. But 2mol e- are required for each mol Cu(s) produced.


Question 10

If the standard free energy change for the reaction

2H2(g) + O2(g) --> 2H2O(l)
is -475 kJ, calculate the standard voltage that could be obtained from a fuel cell utilizing this reaction.

+1.23 V

The half reactions are

O2 + 4H+ + 4e- ----> 2H2O
4H+ + 4e- ----> 2H2
Use the equation DGo = -nFEo.



Question 11

Consider the following cell:

Pb(s)|PbSO4(s)|SO42-(aq, 0.60 M)||H2(g, 192.5 kPa)|H+(aq, 0.70 M)|Pt
If Eo for the cell is 0.36 V at 25oC, write the Nernst equation for the cell at this temperature.

E = 0.36 - 0.01285ln[1.90/{(0.70)2(0.60)}]

The half reactions are

2H+(aq) + 2e- ----> H2(g)
PbSO4(s) + 2e- ----> Pb(s) + SO42-(aq)



Question 12

The rate of formation of NO2(g) in the reaction

2N2O5(g) --> 4NO2(g) + O2(g)
is 5.78 (mol NO2).L-1.s-1. What is the rate at which N2O5 is used?

2.89 (mol N2O5).L-1.s-1

5.78 (mol NO2).L-1.s-1 x (2 mol N2O5)/(4 mol NO2)
= 2.89 (mol N2O5).L-1.s-1



Question 13

Given:

2O3(g) --> 3O2(g) rate = k[O3]2[O2]-1
The overall order of the reaction is

1

Add the superscripts in the rate law.



Question 14

If the rate of a reaction increases by a factor of 64 when the concentration of reactant increases by a factor of 4, the order of the reaction with respect to this reactant is

3

rate = k[concentration]order. Therefore, (4)order = 64 and order = 3.



Question 15

For the reaction

2A + B --> products
determine the rate law for the reaction given the following data:

Initial Concentration, M Initial Rate, M.s-1
A B
0.10 0.10 2.0 x 10-2
0.20 0.10 8.0 x 10-2
0.30 0.10 1.8 x 10-1
0.20 0.20 8.0 x 10-2
0.30 0.30 1.8 x 10-1

rate = k[A]2

When the concentration of B is varied ([A] constant), the rate does not change. When the concentration of A is doubled and tripled ([B] constant), the rate increases by a factor of 4 and 9, respectively. (2)n = 4 and n = 2.



Question 16

A first-order reaction has a rate constant of 0.00300 s-1. The time required for 55% reaction is

266 s

ln[A]t = ln[A]o - kt where [A]t = 1 - 0.55 = 0.45 and [A]o = 1.



Question 17

For a first-order reaction, after 230 s, 10% of the reactants remain. Calculate the rate constant for the reaction.

0.0100 s-1

ln[A]t = ln[A]o - kt where [A]t = 0.1, [A]o = 1 and t = 230 s.



Question 18

Consider the following reaction:

2N2O5(g) ----> 4NO2(g) + O2(g), rate = k[N2O5]
Calculate the time for the concentration of N2O5 to fall to one-eighth its initial value if the rate constant for the reaction is 5.20 x 10-3 s-1.

400 s

ln[A]t = ln[A]o - kt where [A]t = 1/8, [A]o = 1 and k = 0.00520 s-1.



Question 19

The HBr synthesis is thought to involve the following reactions:

Br2 --> 2Br* (1)
Br* + H2 --> HBr + H* (2)
H* + Br2 --> HBr + Br* (3)
2Br* --> Br2 (4)
2H* --> H2 (5)
H* + Br* --> HBr (6)
The chain propagation reactions in this mechanism are reactions

2 and 3

Chain propagation steps involve the reaction of chain carriers or radicals with reactant molecules to produce another chain carrier or radical.



Question 20

For a second-order reaction, a straight line is obtained from a plot of

1/[A]t vs t

For a second-order reaction, 1/[A]t = 1/[A]o + kt.



Question 21

Given: SO2Cl2(g) --> SO2(g) + Cl2(g) rate = k[SO2Cl2]

If 70% of the SO2Cl2 has reacted after 80 s, calculate the rate constant.

0.015 s-1

ln[A]t = ln[A]o - kt where [A]t = 0.3, [A]o = 1 and t = 80 s.



Question 22

For the reaction

cyclopropane --> propene
a plot of ln[cyclopropane] vs time in seconds gives a straight line with slope -2.8 x 10-4 s-1 at 500oC. What is the rate constant for this reaction?

2.8 x 10-4 s-1

For a first-order reaction, the slope of a plot of ln[concentration] vs time is -k.



Question 23

Consider the dimerization reaction below:

2A-->A2 rate = k[A]2
When the initial concentration of A is 2.0 M, it requires 30 min for 60% of A to react. Calculate the rate constant.

4.2 x 10-4 M-1.s-1

The rate law indicates a second-order reaction for which
1/[A]t = 1[A]o +kt where [A]t = 0.80 (40% of A remains), [A]o = 2.0 and t = 30 x 60 s.



Question 24

For the reaction

C2H5Br(aq) + OH-(aq) -->C2H5OH(aq) + Br-(aq)
a plot of lnk versus 1/T gives a straight line with a slope equal to -1.07 x 104 K. What is the activation energy for the reaction?

89.0 kJ/mol

The slope of a plot of lnk versus 1/T is -Ea/R.



Question 25

An elementary process has an activation energy of 40 kJ/mol. If the activation energy for the reverse reaction is 20 kJ/mol, what is the enthalpy change for the reaction?

20 kJ/mol

Because the activation energy of the reverse reaction is less than the activation energy for the forward reaction, the reaction is endothermic in the forward direction. The enthalpy change is 40 - 20 = 20 kJ/mol. See figure 18.35 (a) in the text.



Question 26

A reaction that has a very high activation energy

has a rate that is very sensitive to temperature.

The slope of a plot of lnk vs 1/T is directly proportional to Ea, the activation energy. Therefore, a large activation energy means a large slope and a large change in rate constants with temperature.


Question 27

Given:

O(g) + O3(g) --> 2O2(g)
The rate law for this elementary process is

rate = k[O][O3]

Because this is an elementary reaction, the rate law is the product of the concentration of each species times the rate constant for the reaction.



Question 28

The reaction

NO2(g) + CO(g) --> CO2(g) + NO(g)
is postulated to occur via the mechanism below:
NO2(g) + NO2(g) --> NO3(g) + NO(g) slow
NO3(g) + CO(g)--> NO2(g) + CO2(g) fast
An intermediate in this reaction is

NO3(g)

A reaction intermediate is a species that appears in the mechanism but not in the equation for the overall process. The species NO3(g) does not appear in the overall equation but does appear in the mechanism.