Here is a description of an analytical procedure for superconductors containing unknown quantities of Cu(I),Cu(II), Cu(III), and peroxide (O22-) : 33The possible trivalent copper and/or peroxide type oxygen are reduced by Cu(I) when dissolving the sample (ca .50 mg) in deoxygenated HCl solution ( 1 M) containing a known excess of monovalent copper ions (ca.25mgCuCI) . On the other hand, if the sample itself contained monovalent copper, the amount of Cu(I) in the solution would increase upon dissolving the sample. The excess Cu(I) was then determined by coulometric back titration... in an argon atmosphere." The abbreviation "ca." means "approximately." Coulometry is an electrochemical method in which the electrons liberated in the reactionCu+Cu2++eare measured from the charge flowing through an electrode. Explain with your own words and equations how this analysis works.

Short Answer

Expert verified

The working of this analysis is explained clearly in this problem.

Step by step solution

01

Discuss the concept of the mole.

  • The mole concept is a simple way to express the amount of a substance. Any measurement is divided into two parts: the numerical magnitude and the units in which the magnitude is expressed. For example, if the mass of a ball is 2 kilograms, the magnitude is '2' and the unit is 'kilogram.'
  • When dealing with particles at the atomic (or molecular) level, even one gram of a pure element is known to contain a large number of atoms. This is a common application of the mole concept. It mainly concentrates on the component known as a mole,' which is a count of a very large number of particles.
02

Calculating the moles of  Co3+

To calculate moles of Co3+that are contained in 25.00mg of material we need to calculate moles of Fe2+that reacted withCO3+ .

To do that, we need to subtract initial moles of Fe2+and subtract them with excess (unreacted) moles ofFe2+ .

Initial moles of Fe2+are:

ninitialFe2+=cFe2+.VFe2+ninitialFe2+=0.1000mol/L.5.000×10-3KninitialFe2+=5×10-4mol

To equal the number of electrons on the left and right sides we need to multiply the second equation by 3 and then add reactants and products of each reaction together:

Reduction:Cr2O72-+fre+14H+2Cr3++7H2Ooxidation:6Fe2+6Fe3++6e

Net reaction is:

Cr2O72-+14H++6fe2+2Cr3++7H2O+6Fe3+

The number of moles that reacted with CO3+are then:

nFe2+=ninitialFe2+-nexcessFe2+nFe2+=5×10-4mol-3.085×10-4molnFe2+=1.915×10-4mol

By looking at the reaction of Co3+and Fe2+the ratio they react in is 1:1 so their number of moles are equal. The number of mmoles ofCO3 in 25.00 mg sample is:

nCo3+=nFe2+=1.915×10-4mol=0.1915mmol

03

Substracting the moles of CO with moles of  Co3+

By subtracting total moles of Co with moles of Co3+we can calculate moles of Co2+:

nCo2+=nCo-nCo3+nCo2+=2.393×10-4mol-1.915×10-4mol=4.78×10-5mol

04

Calculating the average oxidation state.

Finally, we can calculate the average oxidation state by using this equation:

average oxidation state =nCo2+.2+nCo3+.3ntotalCo

average oxidation state =4.78×10-5.2+1.915×10-4.32.393×10-4

average oxidation state = 2.80

In the formula Li1+yCoO2, cobalt has an oxidation state 2.8 and oxygen - 4 so we can calculate y by writing this equation:

total oxidation state = Li + Co +2o

0=Li+2.8-4Li=4-2.8Li=1.2

Since the oxidation state of lithium is 1.2 , the value of y is:

1.2=1+yy=1.2-1y=0.2

05

Calculating the theoretical weight percent.

The theoretical weight percent is calculated by dividing the molar mass of the element with the total molar mass of the compound:

WLi,Li1.2CoO2=1.2MLiMLI1.2CoO2.100%WLi,Li1.2CoO2=1.2.6.94g/moT1.2.6.94+1.58.933+2.15.99.100%WLi2,Li1.2CoO2=8.39%

Theoretical quotient wt\% Li/ wt\% Co is:

wLiwCo=0.08390.5938wLiwCo=0.1429

The theoretical value is a little bit higher than the observed value of quotient.

Hence the working of this analysis is explained clearly.

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Most popular questions from this chapter

Aqueous glycerol solution weighing 100.0m gwas treated with 50.0 mL of 0.083 7 M Ce4+in 4 MHCIO4at 60°for15minto oxidize glycerol to formic acid.

CH2-CH-CH2|||OHOHOH HCO2H

Glycerol Formic acid

FM92.095

The excess Ce4+ required 12.11mL of 0.044 8 MFe2+to reach a ferroin end point. Find wt%glycerol in the unknown.

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

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.

A titration of\(50.0\;mL\)of unknown\(F{e^{2 + }}\)with\(0.100MCe\)at\(2{5^\circ }C\), monitored with Pt and calomel electrodes, gave data in the table.\(^9\)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\(F{e^{2 + }}\)in the unknown.

Would indigo tetrasulfonate be a suitable redox indicator for the titration of Fe(CN)64-with TI3+in 1MHCI? (Hint: The potential at the equivalence point must be between the potentials for each redox couple.)

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