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Find E at VCe4+=20.0$ and 51.0 mL.

Short Answer

Expert verified

The potential (E) at VCe4+=20.0mL is 0.1516 V and VCe4+=51.0mL is 1.358V

Step by step solution

01

Definition of Electrode potential

Electrode potential (E) is the electromotive force that exists between two electrodes. Cell consists of two electrode, one is standard electrode (such as calomel electrode and standard hydrogen) (such as calomel electrode and standard hydrogen) where, the potential of an electrode connected to the positive terminal is denoted by the letter and the potential of the electrode attached to the negative terminal is E.

02

Find Electrode potential

Titration:

Ce4+Fe2+→Ce3++Fe3+

Each portion of Ce4+consumes Ce4+and produces an equal number of moles of Ce3+and Fe3+as it is added. Extra unreacted role="math" localid="1663605916802" Fe2+rests in the solution prior to the equivalence point.

The point of equivalence comes at 50.0mL .

Before the equivalence point,

E=E++E=E++Ecalomal=0.526-0.05916logFec2+Fe3+---1

At 20.0 mL :

This is the method to the point of equivalence. As a result, 20.0/50.0 cerium is in the form of Fe3+, while 30.0/50.0 cerium is in the form of Fe3+. Using this value as a substitute in equation (1),

=0.526-0.05916log20/5030/50=0.526-0.05916log1.5=0.526-0.05916×0.1760=0.526-0.0104=0.516V

At 51.0 mL :

E=E++E=E++Ecalomel=1.70-0,05916logCe3+Ce4+-0.241---2

The first 50.0 mL of cerium are converted into Ce3+ and an excess of 1.0mLCe4+ is there. Therefore, Ce3+Ce4+=50.0mL1.0mL. Substitute this value in equation (2),

=1.70-0,05916logCe3+Ce4+-0.241=1.70-0,05916log50.050.1-0.241=1.70-0,05916×1.6989-0.241=1.70-0.1005-0.241=1.5995-0.241=1.358V

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Most popular questions from this chapter

(a) Potassium iodate solution was prepared by dissolving 1.022gof KIO3(FM214.00)in a 500 - mLvolumetric flask. Then 50.00mL of the solution were pipetted into a flask and treated with excess KI (2g) and acid (10mLof0.5MH2SO4) ofHow many moles of fl3- are created by the reaction?

(b) The triiodide from part (a) reacted with 37.66 mL of Na2S2O3solution. What is the concentration of the Na2S2O3 solution?

(c) A 1.223-g sample of solid containing ascorbic acid and inert ingredients was dissolved in dilute H2SO4 and treated with 2g of KI and 50.00mL of KIO3solution from part (a). Excess triiodide required14.22 mLofNa2S2O3solution from part (b). Find the weight percent of ascorbic acid (FM 176.13) in the unknown.

(d) Does it matter whether starch indicator is added at the beginning or near the end point in the titration in part (c)?

H2Swas measured by slowly adding 25.00mLof aqueous H2S to 25.00mL of acidified standard0.01044Ml3-to precipitate elemental sulfur. (If H2S>0.01M, then precipitated sulfur traps somel3-solution, which is not subsequently titrated.) The remainingl3-was titrated with 14.44mL of 0.009336MNa2S2O3. Find the molarity of theH2Ssolution. Should starch indicator be added to this titration at the beginning or just before the end point?

A titration of 50.0 mLof unknown Fe2+with 0.100MCeat 25°C , monitored with Pt and calomel electrodes, gave data in the table. Prepare a Gran plot and decide which data lie on a straight line. Find the x-intercept of this line, which is the equivalence volume. Calculate the molarity of Fe2+in the unknown.

Consider the titration in Figure 16-2.

(a) Write a balanced titration reaction.

(b) Write two different half-reactions for the indicator electrode.

(c) Write two different Nernst equations for the cell voltage.

(d) Calculate E at the following volumes of\(C{e^{4 + }}:10.0,25.0,49.0\), 50.0 .51 .0,60.0, and\(100.0\;mL\). Compare your results with Figure 16-2 .

From the following reduction potentials

l2(s)+2e-⇌2lE°=0.535Vl2(aq)+2c-⇌2l-E°=0.620Vl3+2e-⇌3l3lE°=0.535V

(a) Calculate the equilibrium constant forl2(aq)+l-⇌l3-.

(b)The equilibrium constant for l2(s)+l-⇌l3-.

(c)The solubility (g/L.) of l2(s)in water is.

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