Compute the titration curve for Demonstration 16-1, in which 400.0mLof 37.5mMFe2+ are titrated with 20.0mMMnO4- at a fixed pH of 0.00 in 1MH2SO4 . Calculate the potential versus S.C.E. at titrant volumes of 1.0,7.5,14.0,15.0,16.0, and 30.0 mL and sketch the titration curve.

Short Answer

Expert verified

The titrant volumes are:

1.00mL:0.371V7.5mL:0.439V14.0mL:0.507V15.0mL:1.128V16.0mL:1.252V30.0mL:1.266V

The titration curve is:

Step by step solution

01

Definition of titration curve and titration volume

  • Titrations are frequently graphed as titration curves, with the volume of the titrant as the independent variable and the pH of the solution as the dependent variable (because it changes depending on the composition of the two solutions).
  • Titration is a typical quantitative chemical analysis procedure used in laboratories to quantify the concentration of a specified analyte. The titrant or titrator is a reagent that is made as a standard solution with a known concentration and volume.
02

Determine the potential versus S.C.E. at titrant volumes of 1.0,7.5,14.0,15.0,16.0, and 30.0 mL and sketch the titration curve

The potential vs. S.C.E. at titrant quantities of a particular volume must be computed, and a titration curve created.

Potential of the electrode (E): Electrode potential is the electromotive force between two electrodes. Two electrodes make up a cell: one is a standard electrode (such as calomel electrode or standard hydrogen electrode) and the other is a provided electrode.

E=E+E-

Where,

E+is the electrode's potential when it's linked to the positive terminal

E-is the electrode's potential when it's linked to the negative terminal

Titration:

MnO4-+5Fe2++8H+Mn2++5Fe3++4H2OFe3+e-E0=0.68Vin1MH2SO4MnO4-+8H++5eMn2++4H2OE0=1.507V

At 15.0 mL, the equivalency point is reached.

Prior to the moment of equivalency,

E=E++E-=(0.68-0.05916log|Fe2+|[Fe2+-0.2411.00mL:[Fe2+]/[Fe3+]=14.0/1.0=0.371V7.5mL:[Fe2+]/[Fe3+]=7.5/7.5=0.439V14.0mL:[Fe2+]/[Fe3+]=1.0/4.0=0.507V

Use the electrode potential equation at the equivalence point,

6E4=8.215-0.05916log1[H+]πpH=0

E4=1.369VE=E+E-=1.369V-0.241=1.128V

After the equivalence point,

E=E++E-=1.507-0.059165log|Mn2+||MnO42||H+|N-0.24116.0mL[Mn2+]/[MnO4]=15.0/1.0and[H+]=1M=1.252V30.0mL:[Mn2+)]/[MnO4-]=15.0/15.0and[H+]=1M=1.266V

titration curve must be drawn

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Most popular questions from this chapter

Write balanced half-reactions in which MnO4-acts as an oxidant at

(a)pH=0;(b)pH=10;(c)pH=15.

Two possible reactions of MnO4-withH2O2to produceO2andareMn+

Scheme:MnO4-Mn2+H2O2O2

Scheme:MnO4-O2+Mn2+H2O2H2O

(a) Complete the half reactions for both schemes by adding e+and H2Oand H+write a balanced net equation for each scheme.

(b) Sodium peroxyborate tetrahydrate, NaBO34H2O(FM153.86)produces H2O2when dissolved in acid BO3-+2H2OH2O2+H2BO3-. To decide whether Scheme 1 or 2 Schemeoccurs student at the U.S. Naval academy weighed 0.123gNaBO3.2H2Ointo a 100mLvolumetric flask added 20mLof 1MH2SO4and diluted to the mark with H2O. Then they titratedof this solution with0.01046MKMnO4until the first pale pink color persisted. How may mL ofKMnO4are required in Scheme 1and 2 Scheme?

(The Scheme 1stoichiometry was observed).

Calcium fluorapatite(Ca10(PO4)6F2,FM1008.6)laser crystals were doped with chromium to improve their efficiency. It was suspected that the chromium could be in the+4oxidation state.

  1. To measure the total oxidizing power of chromium in the material, a crystal was dissolved in 2.9MHCLO4 at 100°C, cooled to 20°C , and titrated with standard Fe2+ , using Pt and Ag - AgCl electrodes to find the end point. Chromium above the 3 + state should oxidize an equivalent amount of Fe2+ in this step. That is,Cr4+would consume one Fe2+ , and Cr6+in Cr2O72- would consume three Fe2+ :

role="math" localid="1664873864085" Cr4++Fe2+Cr3++Fe3+12Cr2O72-+3Fe2+Cr3++3Fe3+

2. In a second step, the total chromium content was measured by dissolving a crystal in 2.9MHCLO4 at and cooling to 20°C . Excess and were then added to oxidize all chromium to Cr2O72- . Unreacted S2O8-2was destroyed by boiling, and the remaining solution was titrated with standard Fe2+ . In this step, each Crin the original unknown reacts with three Fe2+ .

Crx++S2O82-Cr2O72-12Cr2O72-+3Fe2+Cr3++3Fe3+

In Step 1,0.4375g of laser crystal required 0.498mL of (prepared by dissolving in ). In step , of crystal required of the same solution. Find the average oxidation number of in the crystal and find the total micrograms ofpre gram of crystal.

Winkler titration for dissolved O2.Dissolved O2 is a prime indicator of the ability of a body of natural water to support aquatic life. If excessive nutrients run into a lake from fertilizer or sewage, algae and phytoplankton thrive. When algae die and sink to the bottom of the lake, their organic matter is decomposed by bacteria that consume O2from the water. Eventually, the water can be sufficiently depleted ofO2so that fish cannot live. The process by which a body of water becomes enriched in nutrients, some forms of life thrive, and the water eventually becomes depleted ofO2is called eutrophication. One way to measure dissolvedO2 is by the Winkler method that involves an iodometric titration: 35

Dissolved oxygen or biochemical oxygen demand

1. Collect water in a ~300mLbottle with a tightly fitting, individually matched ground glass stopper. The manufacturer indicates the volume of the bottle (±0.1mL)with the stopper inserted on the bottle. Submerge the stoppered bottle at the desired depth in the water to be sampled. Remove the stopper and fill the bottle with water. Dislodge any air bubbles before inserting the stopper while the bottle is still submerged.

2. Immediately pipet 2.0 mL of 2.15MMnSO4and 2.0 mL of alkali solution containing500gNaOH/L,135gNaL/L and 10gNaN3/L (sodium azide). The pipet should be below the liquid surface during addition to avoid introducing air bubbles. The dense solutions sink and displace close to 4.0 Ml of natural water from the bottle. 3. Stopper the bottle tightly, remove displaced liquid from the cup around the stopper, and mix by inversion. O2is consumed andMn(OH)3 precipitates:

4Mn2++O2+8OH-+2H2O4Mn(OH)3(s)

Azide consumes any nitrite(NO2-)in the water so that nitrite cannot subsequently interfere in the iodometric titration:

2NO2-+6N3-+4H2O10N2+8OH-

4. Back at the lab, slowly add 2.0 mL of 18MH2SO4below the liquid surface, stopper the bottle tightly, remove the displaced liquid from the cup, and mix by inversion. Acid dissolves which reacts quantitatively with

2Mn(OH)3(s)+3H2SO4+3I-2Mn2++I3-+3SO42-+6H2O

5. Measure 200.0 mLof the liquid into an Erlenmeyer flask and titrate with standard thiosulfate. Add 3mL of starch solution just before the end point and complete the titration.

A bottle of 297.6 mLof water from a creek at0°Cin the winter was collected and required 14.05 mL 10.22 mM thiosulfate.

(a) What fraction of the 297.6 mL sample remains after treatment with and alkali solution?

(b) What fraction remains after treatment with H2SO4? Assume that H2SO4sinks into the bottle and displaces 2.0 mL of solution prior to mixing.

(c) How many mL of the original sample are contained in the 200.0 mLthat are titrated?

(d) How many moles ofl3- are produced by each mole ofO2 in the water?

(e) Express the dissolved O2content in (f) Pure water that is saturated with O2 contains 14.6mgO2/Lat0°C. What is the fraction of saturation of the creek water with O2?

(g) Write a reaction of NO2-withl- that would interfere with the titration ifN3-were not introduced. See Table 16-5.

Ascorbic acid (0.0100M)was added to 10.0mL of 0.0200MFe3+at pH 0.30, and the potential was monitored with Pt and saturated Ag | AgClelectrodes.

Dehydroascorbic acidrole="math" localid="1664865837362" +2H++2e-ascorbicacid+H2OE°=0.390V

(a) Write a balanced equation for the titration reaction,

(b) Using E0=0.767V for the role="math" localid="1664865912877" Fe3+Fe2+ couple, calculate the cell voltage when 5.0,10.0 and 15.0 mL of ascorbic acid have been added. (Hint: Refer to the calculations in Demonstration 16 - 1.)

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