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A sample containing La3+ was treated with sodium oxalate to precipitateLa2(C2O4)3 which was washed, dissolved in acid and titrated with 18.04mL of0.006363MKMnO4 . Write the titration reaction and find[La3+] in the unknown.

Short Answer

Expert verified

The titration reaction is 5C2O42-+2MnO4+16H+→10CO2+2Mn2++8H2O. The concentration of La3+is 2.826mM .

Step by step solution

01

Define redox titration.

A redox titration happens when the analyte and the titrant undergo an oxidation–reduction process. The endpoint is frequently detected using an indicator, much as it is in acid–base titrations. Oxalic acid titrated against potassium permanganate in acid medium is an example of redox titration.

02

Find the final equation.

First we need to write the redox reactions. In acidic conditions KMnO4is reduced to Mn2+and C2O42- is oxidized to .

Reduction: MnO4-+8H++5e-→Mn2++4H2O×2

Oxidation: C2O42-→2CO2+2e-×5

To balance the electrons on the left and right side, we multiply the first reaction with and the second reaction with and we get the final equation:

role="math" localid="1663604875571" 5C2O42-+2MnO4+16H+→10CO2+2Mn2++8H2O

Hence the final equation is 5C2O42-+2MnO4+16H+→10CO2+2Mn2++8H2O.

03

Find the concentration of La3+ .

V(KMnO4)=18.04mlc(KMnO4)=0.006363M

Now we can calculate the moles of oxalate used, by using the following relation:

nC2O42-=52·nKMnO4=52×VKMnO4×cKMnO4=52×0.006363mol/L×18.04mL=0.287mmol.

The moles of La3+:

nLa3+=23×nC2O42-=23×0.287mmol=0.1913mmol

Finally we can calculate the concentration of La3+using the following relation:

c(La3+)=n(La3+)V(solution)=0.1913mmol50.00mL=3.826mM

Hence the concentration of La3+is 3.826mM.

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Most popular questions from this chapter

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.

In which technique, iodimetry or iodometry, is starch indicator not added until just before the end point? Why?

Consider the titration of 25.0mLof 0.100M Sn2+ by 0.0500 MT3+in 1MHCI, using Pt and saturated calomel electrodes to find the end point.

(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 ofTl3+:1.00,2.50,4.90,5.00,5.10and 10.0 mL. Sketch the titration curve.

When 25.00mLof unknown were passed through a Jones reductor, molybdate ion(MoO42-)was converted into. The filtrate required 16.43mLof0.01033MKMnO4to reach the purple end point.

role="math" localid="1663608295687" MnO4-+Mo3+→Mn2++MoO22+

A blank required. Balance the reaction and find the molarity of Molybdate in the unknown.

Warning! The Surgeon General has determined that this problem is hazardous to your health. The oxidation numbers of CUand Biin high-temperature superconductors of the type Bi2Sr2(Ca0xYa2)Cu2Ox(which could contain Cu2+,Cu3+,Bi3+ and Bi3+) can be measured by the following procedure. In Experiment, the superconductor is dissolved in 1MHClcontaining excess 2mMCuCl2Bi5+(written as BiO3-) and Cu3+ consume Cu+ to make Cu2+:

BiO3−+2Cu++4H+→BiO++2Cu2++2H2OCu3++Cu+→2Cu2+

The excess, unreactedCu4is then titrated by coulometry (described in Chapter). In Experiment , the superconductor is dissolved in1mMFeCl2â‹…4H2Ocontaining excessBi5+. reacts with therole="math" localid="1668352055227" Fe2+ butCu3+ does not react withdata-custom-editor="chemistry" Fe2+41.

role="math" localid="1668352140519" BiO3−+2Fe2++4H+→BiO++2Fe3++2H2OCu3++12H2O→Cu2++14O2+H+

The excess, unreacted is then titrated by coulometry. The total oxidation number of is measured in Experiment, and the oxidation number ofis determined in Experiment. The difference gives the oxidation number of.

(a) In Experiment AA2, a sample of Bi2Sr2CaCu2O5(FM760.37+15.9994x)(containing no yttrium) weighing 102.3mg was dissolved in 100.0mLof 1MHCl containing 2.000mMCuCl. After reaction with the superconductor, coulometry detected 0.1085 mmolof unreactedCu+ in the solution. In Experiment B, 94.6 mgof superconductor were dissolved in 100.0mL. of 1MHCl containing1.000mMFeCl-4H2O. After reaction with the superconductor, coulometry detected 0.0577 mmolof unreacted. Find the average oxidation numbers of Biand Cuin the superconductor and the oxygen stoichiometry coefficient, x.

(b) Find the uncertainties in the oxidation numbers and x if the quantities in Experiment Aare102.3(±0.2)mgand0.1085(±0.0007)mmoland the quantities in Experiment Bare94.6(±0.2)me and0.0577(±0.0007)mmol. Assume negligible uncertainty in other quantities.

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