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Airida [17]
2 years ago
4

A voltaic cell employs the following redox reaction: 2Fe3+(aq)+3Mg(s)→2Fe(s)+3Mg2+(aq) Calculate the cell potential at 25 ∘C und

er each of the following conditions. A voltaic cell employs the following redox reaction: 2Fe3+(aq)+3Mg(s)→2Fe(s)+3Mg2+(aq) Calculate the cell potential at 25 ∘C under each of the following conditions.
Chemistry
1 answer:
lana [24]2 years ago
4 0

Answer:

1st condition: <u>  E = 2.25 V</u>

<u />

2nd condition <u>=    E = 2.41 V</u>

Explanation:

A voltaic cell employs the following reaction: 2Fe3+(aq) +3Mg(s)→2Fe(s)+3Mg2+(aq) Calculate cell potential at 25 ∘C under each condition?

1st condition: [Fe3+]= 1.6* 10^−3 M ; [Mg2+]= 2.05 M

2nd condition: [Fe3+]= 2.05 M ; [Mg2+]= 1.6*10^−3 M

Step 1: Data given

Temperature = 25 °C

The reduction potential for  Fe+3 →  Fe(s) =   -0.037  

The reduction potential for  Mg+2 +  2e- →  Mg(s) = +2.356

Step 2: The balanced equation

2Fe3+(aq)+3Mg(s)→2Fe(s)+3Mg2+(aq)

Step 3:

Fe+3   +  3e-→  Fe(s)    -0.037

Mg(s) → Mg+2 + 2e-        +2.356

We have to multiply the first equation by 2 and thesecond equation by 3

2Fe+3   +  6e-→  2Fe(s)    (-0.037 )

3Mg(s) → 3Mg+2 + 6e-        (+2.356 )

2Fe+3  +   3Mg  →  2Fe(s)   +  3Mg+2     E°= +2.319  

Step 4:  Calculate the cell potential for the first condition

Nernst Equation:   E = E° – 0.0592/n  *log [Mg+2]³/ [Fe+3]²  

⇒with n = the number of electrons = 6

⇒with [Mg+2] = 2.05 M

⇒with [Fe+3] = 1.6 * 10^-3 M

E = +2.319 -  0.0592/6 * log  ((2.05)³/ (1.6  x 10^-3)² )

 E = +2.319 -  0.0592/6 * 6.53

E = 2.319 - 0.0099 *6.53

<u>  E = 2.25 V</u>

Step5 : Calculate the cell potential for the second condition

Nernst Equation:   E = E° – 0.0592/n  *log [Mg+2]³/ [Fe+3]²  

⇒with n = the number of electrons = 6

⇒with [Fe^3+] = 2.05 M

⇒with [[Mg+2] = 1.6 * 10^-3 M

E = +2.319 -  0.0592/6 * log  ((1.6  x 10^-3)³/ (2.05)² )

 E = +2.319 -  0.0592/6 * (-9.0)

<u>   E = 2.41 V</u>

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Answer:

The correct answer is: pH = 12.73

Explanation:

The <em>neutralization reaction</em> between HCl and KOH is given by the following chemical equation:

HCl + KOH ⇒ KCl + H₂O

Since HCl is a strong acid and KOH is a strong base, HCl is completely dissociated into H⁺ and Cl⁻ ions, whereas KOH is dissociated completely into K⁺ and OH⁻ ions.

For acids, the number of equivalents is given by the moles of H⁺ ions (in this case: 1 equivalent per mol of HCl). For bases, the number of equivalents is given by the moles of OH⁻ ions (in this case: 1 equivalent per mol of KOH).

The H⁺ ions from HCl will react with OH⁻ ions of KOH to give H₂O. The pH is calculated from the difference between the equivalents of H⁺ and OH⁻:

equivalents of H⁺= volume HCl x Molarity HCl

                            = (15.0 mL x 1 L/1000 mL) x 0.100 mol/L

                            = 1.5 x 10⁻³ eq H⁺

equivalents of OH⁻= volume KOH x Molarity KOH

                               = (50.0 mL x 1 L/1000 mL) X 0.100 mol/L

                               = 5 x 10⁻³ eq OH⁻

There are more OH⁻ ions than H⁺ ions. The excess of OH⁻ (that did not react with H⁺ ions) is calculated as follows:

OH⁻ ions= (5 x 10⁻³ eq OH⁻) -  (1.5 x 10⁻³ eq H⁺) = 3.5 x 10⁻³ eq OH⁻= 3.5 x 10⁻³ moles OH⁻  

As the volumes of the solutions are additive, the total volume of the solution is:

V= 15.0 mL + 50.0 mL = 65.0 mL= 0.065 L

So, the concentration of OH⁻ ions in the solution is given by:

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From  [OH⁻], we can calculate pOH:

pOH = -log [OH⁻] = -log (0.054) = 1.27

Finally, we know that pH + pOH= 14; so we calculate pH:

pH= 14 - pOH = 14 - 1,27 =  12.73                                                            

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1) Answer is: the ionic compound in the solution b is K₂CrO₄ (potassium chromate).

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2 · (+1) + 6 + x · (-2) = 0.

x = 4; number of oxygen atoms.

2) Answer is: the ionic compound in solution a is AgNO₃ (silver nitrate).

ω(N) = 8.246% ÷ 100%.

ω(N) = 0.08246; mass percentage of nitrogen.

M(MNO₃) = M(N) ÷ ω(N).

M(MNO₃) = 14 g/mol ÷ 0.08246.

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M(M) = M(MNO₃) - M(N) - 3 · M(O).

M(M) = 169.8 g/mol - 14 g/mol - 3 · 16 g/mol.

M(M) = 107.8 g/mol; atomic mass of metal, this metal is silver (Ag).

3) Balanced chemical reaction:  

2AgNO₃(aq) + K₂CrO₄(aq) → Ag₂CrO₄(s) + 2KNO₃(aq).

Ionic reaction:  

2Ag⁺(aq) + 2NO₃(aq) + 2K⁺(aq) + CrO₄²⁻(aq) → Ag₂CrO₄(s) + 2K⁺(aq) + 2NO₃⁻(aq).

Net ionic reaction: 2Ag⁺(aq) + CrO₄²⁻(aq) → Ag₂CrO₄(s).

Answer is: the blood-red precipitate is silver chromate (Ag₂CrO₄).

4) m(Ag₂CrO₄) = 331.8 g; mass of solid silver chromate.

n(Ag₂CrO₄) = m(Ag₂CrO₄) ÷ M(Ag₂CrO₄).

n(Ag₂CrO₄) = 331.8 g ÷ 331.8 g/mol.

n(Ag₂CrO₄) = 1 mol; amount of silver chromate.

From balanced chemical reaction: n(Ag₂CrO₄) : n(AgNO₃) = 1 : 2.

n(AgNO₃) = 2 · 1 mol.

n(AgNO₃) = 2 mol.

m(AgNO₃) = n(AgNO₃) · M(AgNO₃).

m(AgNO₃) = 2 mol · 169.8 g/mol.

m(AgNO₃) = 339.6 g; mass of silver nitrate.

m(AgNO₃) = m(K₂CrO₄).

m(K₂CrO₄) = 339.6 g; mass of potassium chromate.

n(K₂CrO₄) = m(K₂CrO₄) ÷ M(K₂CrO₄).

n(K₂CrO₄) = 339.6 g ÷ 194.2 g/mol.

n(K₂CrO₄) = 1.75 mol; amount of potassium chromate.

5) Chemical reaction of dissociation of silver nitrate in water:

AgNO₃(aq) → Ag⁺(aq) + NO₃⁻(aq).

V(solution a) = 500 mL ÷ 1000 mL/L.

V(solution a) = 0.5 L; volume of solution a.

c(AgNO₃) = n(AgNO₃) ÷ V(solution a).

c(AgNO₃) = 2 mol ÷ 0.5 L.

c(AgNO₃) = 4 mol/L = 4 M.

From dissociation of silver nitrate: c(AgNO₃) = c(Ag⁺) = c(NO₃⁻).

c(Ag⁺) = 4 M; the concentration of silver ions in the original solution a.

c(NO₃⁻) = 4 M; the concentration of silver ions in the original solution a.

6) Chemical reaction of dissociation of potssium chromate in water:

K₂CrO₄(aq) → 2K⁺(aq) + CrO₄²⁻(aq).

V(solution b) = 500 mL ÷ 1000 mL/L.

V(solution b) = 0.5 L; volume of solution b.

c(K₂CrO₄) = n(K₂CrO₄) ÷ V(solution b).

c(AgNO₃) = 1.75 mol ÷ 0.5 L.

c(AgNO₃) = 3.5 mol/L = 3.5 M.

From dissociation of silver nitrate: c(K₂CrO₄) = c/2(K⁺) = c(CrO₄²⁻).

c(K⁺) = 7 M; the concentration of potassium ions in the original solution b.

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