#4 Chem Lab Report - Agustin

Download as pdf or txt
Download as pdf or txt
You are on page 1of 6

EXPERIMENT # 4

GALVANIC CELLS, THE NERST EQUATION

NAME: AGUSTIN, SETH JARL G. CM011L/A3

PROGRAM/YEAR: CE - 1 DOP: APRIL 9, 2020

GROUP N0. 3 DOS: APRIL 25, 2020

PRELIM DATA SHEET: /50

COVER: /10

OBJECTIVE: /10

REPORT SHEET: /20

CONCLUSION: /10

ELIZABETH ESPIRITU TOTAL: /100


PROFFESOR
EXPERIMENT # 4
GALVANIC CELLS, THE NERST EQUATION

OBJECTIVES:

1. TO MEASURE THE RELATIVE REDUCTION POTENTIALS


FOR A NUMBER OF REDOX COUPLES.DFDFDFDFDFCV
VXXCVXCVXCVXCVXVXC VXCVXCVXC
2. TO DEVELOP AN UNDERSTANDING OF THE
MOVEMENT OF ELECTRONS, ANIONS, AND CATIONS
IN A GALVANIC CELL. DFDFDFD
DSDSDSDSDSDSDS
3. TO STUDY FACTORS AFFECTING CELL POTENTIALS.
DDFDFDF
4. TO ESTIMATE THE CONCENTRATION OF IONS IN
SOLUTION USING THE NERNST EQUATION.
PRELABORATORY ASSIGNMENT:
1. In a galvanic cell,
a. Oxidation occurs at the (name of electrode) Anode

b. The Cathode is the (sign) electrode Positive Electrode

c. Cations flow in solution toward the (name of electrode) Cathode

d. electrons flow from the (name of electrode) to (name of electrode) Anode to Cathode

2. a. What is the purpose of a salt bridge? Explain.


The salt bridge allows ions to flow without extensive mixing of the
solutions. It allows ion flow but prevents extensive mixing of solutions in
oxidation and reduction compartments. Without Salt Bridge, there will be an
accumulation of charge in both the compartments, thus no flow of electron
and current. Therefore, to keep the net charge zero in each compartment,
Salt Bridge is necessary.

b. How is the salt bridge prepared in this experiment?


A filter paper was rolled and flattened, then wet with a 0.1 M KNO₃ solution.
Afterwards, folded and inserted the ends of it into the solutions unto the
two beakers.

3. Experimental Procedure, Part C.1. A 1-mL pipet is used to transfer 1.0-mL of a


0.10 M CuSO₄ solution to a 100-mL volumetric flask. The volumetric flask is then
filled to the mark with deionized water. See figure 32.6. What is the molar
concentration of the diluted solution? Show calculations expressing the
concentration with the correct number of significant figures.
4. Refer to Figure 32.2 and equations 32.8 and 32.9.

a. What is the value of the cell constant (y-intercept)?


E𝒸ₑₗₗ = constant – 0.0592/2 (pCu)
0.95 V = constant – 0.0592/2 (6)
Constant = 1.1276

b. What is the [Cu²⁺] if the measured cell potential is 1.05 V?


E𝒸ₑₗₗ = constant + 0.0592/2 (log[Cu²⁺])
1.05 V = 1.1276 + 0.0592/2 (log[Cu²⁺])
[Cu²⁺] = 2.39 mol/L

c. What should be the cell potential if the [Cu²⁺] is 1.0 x 10⁻⁶ mol/L?
E𝒸ₑₗₗ = constant + 0.0592/2 (log[Cu²⁺])
= 1.1276 + 0.0592/2 ( log 1.0 x 10⁻⁶ mol/L)
= 1.04 V

5. Consider a galvanic cell consisting of the following two redox couples:

Ag⁺(0.010 M) + e⁻ ⇒ Ag(s) E° = +0.80 V


Cr³⁺(0.010 M) + 3e⁻ ⇒ Cr(s) E° = -0.74 V

a. Write the equation for the half-reaction occuring at the


dd cathode.
Ag⁺(aq) + e⁻ ⇒
Ag(s)

b. Write the equation for the half-reaction occuring at the


dd anode.
Cr(s) ⇒ Cr³⁺(aq) + 3e⁻

c. Write the equation for cell reaction.


Cr(s) + 3Ag⁺(aq) ⇒ Cr³⁺(aq) + 3Ag(s)

d. What is the standard cell potential, E°𝒸ₑₗₗ, for the cell?


E°𝒸ₑₗₗ = E°(Ag⁺/Ag) - E°(Cr³⁺/Cr)
= 0.80 V - (-0.74 V)
= 1.54 V

e. Realizing the nonstandard concentration, what is the actual cell potential, E°𝒸ₑₗₗ, for the cell? See
equation 32.6. Hint: What is the value of n in the Nernst equation?
E°𝒸ₑₗₗ = E°𝒸ₑₗₗ - RT/nF ln([Cr³⁺]/[Ag⁺]³)
= 1.54 - 8.314 x 298.15 / (3 x 96485) x ln(0.010 / 0.010³)
= 1.46 V
6. The extend of corrossion in the steel reinforcing rods (rebar) of concrete is
measured by the galvanic cell shown in the diagram of the instrument. The half-cell
of the probe is usually a AgCl/Ag redox couple:

AgCl + e⁻ ⇒ Ag + Cl⁻ ( 1.0 M) E° = +0.23 V

Corrosion is said to be severe if the cell potential is


measured at greater than 0.41 V. Under these
conditions, what is the iron(II) concentration on the
rebar? See equation 32.6

Fe²⁺ + 2e⁻ ⇒ Fe E° = -0.44 V

Iron(II) Concentration on the Rebar


CONCLUSION:

In this experiment, our main focus is the galvanic cell or volataic


cell, which is an electrochemical cell that produces electricity
through chemical reactions between dissimilar conductors connected
through an electrolyte and a salt bridge. The reaction that makes the
production of electrical energy possible in a galvanic cell is called an
oxidation-reduction reaction or redox. The important parts of a
galvanicic cell are the anode and the cathode. The anode is an
electrode where oxidation occurs while the cathode is an electrode
where reduction occurs. However this alone will not produce
electrical energy for the reason that there is the existence of charge
build up. Therefore, we need a salt bridge which is a chamber of
electrolytes necessary to complete the circuit of a galvanic cell. The
strength of electrical potential in a galvanic cell depends on the
reducing agent and oxidizing agent used. If both a strong reducing
agent and oxidizing agent is used, then a strong electrical potential
is also produced. The concentration of solution also affects the
electrical potential of a galvanic cell depending on how concentrated
it is. By browsing through the "Standard Electrode Potentials in
Aqueous Solution at 25°C" chart, one can make different
combinations of making a galvanic cell. In addition, a galvanic cell
also produces ions which are anions and cation. Anion flows to the
anode while cation flows to cathode. These ion flow in order to
balance the charges in both half reactions, that is why electrons flow
from the anode to the cathode through an external wire in a galvanic
cell.

You might also like