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mylen [45]
4 years ago
10

Calculate the cell potential E at 25°C for the reaction 2 Al(s) + 3 Fe2+(aq) → 2 Al3+(aq) + 3 Fe(s) given that [Fe 2+] = 0.020 M

, [Al 3+] = 0.10 M, and the standard reduction potential is -1.66 V for Al 3+/Al and -0.45 V for Fe 2+/Fe.
Chemistry
1 answer:
Elodia [21]4 years ago
5 0

Answer:

1.18 V

Explanation:

The given cell is:

Al(s)/Al^{3+}(0.10M)||Fe^{2+}(0.020M)/Fe(s)

Half reactions for the given cell follows:

Oxidation half reaction: Al(s)\rightarrow Al^{3+}(0.10M)+2e^-;E^o_{Al^{3+}/Al}=-1.66V

Reduction half reaction: Fe^{2+}(0.020M)+2e^-\rightarrow Fe(s);E^o_{Fe^{2+}/Fe}=-0.45V

Multiply Oxidation half reaction by 2 and Reduction half reaction by 3

Net reaction: 2Al(s)+3Fe^{2+}(0.020M)\rightarrow 2Al^{3+}(0.10M)+3Fe(s)

Oxidation reaction occurs at anode and reduction reaction occurs at cathode.

To calculate the E^o_{cell} of the reaction, we use the equation:

E^o_{cell}=E^o_{cathode}-E^o_{anode}

Putting values in above equation, we get:

E^o_{cell}=-0.45-(-1.66)=1.21V

To calculate the EMF of the cell, we use the Nernst equation, which is:

E_{cell}=E^o_{cell}-\frac{0.059}{n}\log \frac{[Al^{3+}]^2}{[Fe^{2+}]^3}

where,

E_{cell} = electrode potential of the cell = ?V

E^o_{cell} = standard electrode potential of the cell = +1.21 V

n = number of electrons exchanged = 6

Putting values in above equation, we get:

E_{cell}=1.21-\frac{0.059}{6}\times \log(\frac{0.10^2}{0.020^3})\\\\E_{cell}=1.18V

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Anastaziya [24]

Answer:

[∝] = +472

Explanation:

Specific rotation in a solution is defined as:

[∝] = ∝ / c×l

Where:

[∝] is specific rotation, ∝ is observed rotation (In degrees), c is concentration in g/mL and l is path length (In dm).

∝: +47.2°

c: 2.0g / 50mL = 0.04g/mL

l: 25cm × (1dm /10cm) = 2.5dm

Replacing:

[∝] = +47.2° / 0.04g/mL×2.5dm = <em>+472</em>

I hope it helps!

4 0
3 years ago
Sulfur dioxide, SO 2 ( g ) , can react with oxygen to produce sulfur trioxide, SO 3 ( g ) , by the reaction 2 SO 2 ( g ) + O 2 (
aleksley [76]

<u>Answer:</u> The amount of heat produced by the reaction is -21.36 kJ

<u>Explanation:</u>

Enthalpy change is defined as the difference in enthalpies of all the product and the reactants each multiplied with their respective number of moles.

The equation used to calculate enthalpy change is of a reaction is:

\Delta H^o_{rxn}=\sum [n\times \Delta H_f_{(product)}]-\sum [n\times \Delta H_f_{(reactant)}]

For the given chemical reaction:

2SO_2(g)+O_2(g)\rightarrow 2SO_3(g)

The equation for the enthalpy change of the above reaction is:

\Delta H_{rxn}=[(2\times \Delta H_f_{(SO_3(g))})]-[(2\times \Delta H_f_{(SO_2(g))})+(1\times \Delta H_f_{(O_2(g))})]

We are given:

\Delta H_f_{(SO_2(g))}=-296.8kJ/mol\\\Delta H_f_{(SO_3(g))}=-395.7kJ/mol\\\Delta H_f_{(O_2(g))}=0kJ/mol

Putting values in above equation, we get:

\Delta H_{rxn}=[(2\times (-395.7))]-[(2\times (-296.8))+(1\times (0))]\\\\\Delta H_{rxn}=-197.8kJ/mol

To calculate the number of moles, we use ideal gas equation, which is:

PV=nRT

where,

P = pressure of the gas = 1.00 bar

V = Volume of the gas = 2.67 L

n = number of moles of gas = ?

R = Gas constant = 0.0831\text{ L. bar }mol^{-1}K^{-1}

T = temperature of the mixture = 25^oC=[25+273]K=298K

Putting values in above equation, we get:

1.00bar\times 2.67L=n\times 0.0831\text{ L. bar }mol^{-1}K^{-1}\times 298K\\\\n=\frac{1\times 2.67}{0.0831\times 298}=0.108mol

To calculate the heat released of the reaction, we use the equation:

\Delta H_{rxn}=\frac{q}{n}

where,

q = amount of heat released = ?

n = number of moles = 0.108 moles

\Delta H_{rxn} = enthalpy change of the reaction = -197.8 kJ/mol

Putting values in above equation, we get:

-197.8kJ/mol=\frac{q}{0.108mol}\\\\q=(-197.8kJ/mol\times 0.108mol)=-21.36kJ

Hence, the amount of heat produced by the reaction is -21.36 kJ

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Explanation:

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