A 3.026-g portion of a copper(II) salt was dissolved in a 250-mL volumetric flask. A 50.0-mL aliquot was analyzed by adding of KI and titrating the liberated iodine with 23.33mL of 0.04668MNa2S2O3Find the weight percent of Cu in the salt. Should starch indicator be added to this titration at the beginning or just before the end point?

Short Answer

Expert verified

The weight percent of Cu in the salt is 11.45% .Starch should be added right before the equivalence point so that the triiodide doesn’t bind to it during the reaction, Since we have a iodometric titration in the task.

Step by step solution

01

Calculating the weight percent of salt.

The Weight Percentage is simply the ratio of a solute's mass to the mass of a solution multiplied by 100. The Weight Percentage is also referred to as the Mass Percentage.

percentbyweight=gramofsolute100gofsolution

02

Adding starch indicator.

In this task we have a type of iodometric titration. lodide reacts with Cu2+and triiodide is formed:

2Cu2++5l-3Cil+l3-(1)

Triiodide is then titrated with thiosulfate and as we can see in equation 16-19, thiosulfate is oxidized to tetrathionate:

l3-+2S2O32-3l-+S4O62-(2)

To calculate the weight percent of copper, first we need to calculate the number of moles of copper. To do that we can calculate moles of triiodide from thiosulfate and then moles of copper from triiodide.

As we can see in reaction (2), triiodide and thiosulfate react in ratio 1:2 so we can write:

n(l3-)=12n(S2O32-)n(l3-)=12c(S2O32-).V(S2O22-)n(l3-)=120.04668mol/L.23.33×10-3Ln(l3-)=5.45×10-4mol

03

Recalculating the moles of triiodide to copper.

To recalculate the moles of triiodide to copper, we have to take into account the ratio that copper and triiodide react in and that is so we can write:

n(Cu2+)=2.n(l3-)n(Cu2+)=2.5.45×10-4moln(Cu2+)=1.09×10-3mol

Since we can see in the task that Cu2+was dissolved 250mL in but only was took for iodometric titration we have to recalculate the number of moles from 50mL to 250mL

250mLx=50mL1.09×10-3mol

By cross multiplying we get:

x.50mL=250mL.1.09×10-3mol/:50mLx=250arL.1.09×10-3mol50mL

Moles of copper in 250mL solution

x=n(Cu2+)=5.45×10-3mol

Now we can calculate the weight perfect of copper in the salt:

w(copper,salt)=m(copper)m(salt).100%w(copper,salt)=m(copper).M(copper)m(salt).100%w(copper,salt)=5.45×10-3.proT.63.546g/noT3.026g100%w(copper,salt)=11.45%

Since we have a iodometric titration in the task,starch should be added right before the equivalence point so that the triiodide doesn’t bind to it during the reaction.Therefore the weight percent of Cu in the salt is 11.45% .

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Most popular questions from this chapter

The pathogenic bacterium Salmonella enterica uses tetrathionate found in the human gut as an oxidant- just as we useO2to metabolize our food. Write the half-reaction in which tetrathionate serves as an oxidant. Is tetrathionate as powerful an oxidant asO2?

(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)?

Why don'tCr3+and TiO2+interfere in the analysis of Fe3+when a Walden reductor, instead of a Jones reductor, is used for pre-reduction?

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.

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).

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