Coulometric titration of sulfite in wine. Sulfur dioxide is added to many foods as a preservative. In aqueous solution, the following species are in equilibrium:

Bisulfite reacts with aldehydes in food near neutral pH:


Sulfite is released from the adduct in 2MNaOH and can be analyzed by its reaction with I3- to give I-and sulfate. ExcessI3- must be present for quantitative reaction.

Here is a coulometric procedure for analysis of total sulfite in white wine. Total sulfite means all species in Reaction and the adduct in Reaction . We use white wine so that we can see the color of a starch-iodine end point.

1. Mix 9.00 mL of wine plus 0.8gNaOH and dilute to 10.00mL. The releases sulfite from its organic adducts.

2. Generate I3-at the working electrode (the anode) by passing a known current for a known time through the cell in Figure 17 - 10. The cell containsofacetate buffer () plus. In the cathode compartment, is reduced to H2+OH-. The frit retards diffusion of into the main compartment, where it would react with I3- to giveIO-.

3. Generate I3- at the anode with a current of for.

4. Inject 2.000mL of the wine/ solution into the cell, where the sulfite reacts with leaving excess.

5. Add of thiosulfate to consume by Reaction and leave excess thiosulfate.

6. Add starch indicator to the cell and generate freshI3- with a constant current of 10.0mA. A time of 131s was required to consume excess thiosulfate and reach the starch end point.

(a) In what pH range is each form of sulfurous acid predominant?

(b) Write balanced half-reactions for the anode and cathode.

(c) At pH 3.7, the dominant form of sulfurous acid isand the dominant form of sulfuric acid is HSO42-. Write balanced reactions between andand between I3-and HSO3-thiosulfate.

(d) Find the concentration of total sulfite in undiluted wine.

Short Answer

Expert verified
  1. When pH <1.86 theH2SO3 is predominant.
  2. The balanced half-reactions are:H2O+e1/2H2+OH .
  3. The balanced reactions between and :I3andHSO3

I3+HSO3+H2O3I+SO42+3H+

The balanced reactions between and thiosulfate

I3+2S2O32S4O62+3I.

  1. The concentration of total sulphite in undiluted wine is .

Step by step solution

01

Deifinition of titration.

Titration is a method or procedure for estimating the concentration of a dissolved material by calculating the least quantity of known-concentration reagent necessary to produce a particular effect in interaction with a known volume of the test solution.

02

Step 2: The range in which sulphurous acid is predominant.

a)

Equilibrium, H2SO3pK1HSO3pK2SO32

The pK1is 1.86 , while the pK2is 7.17 .

So, when pH < 1.86 the H2SO3is predominant.

When pH range is between and , the dominant form is .

When pH > 7.17, the dominant form isSO32- .

03

Step 3: The balanced half-reactions for the anode and cathode.

b)

The anode's balanced half-reactions are:31I3+2e

For the cathode, the balanced half-reactions are: H2O+e1/2H2+OH.

04

Step 4: The balanced reactions between  and  and between  and thiosulfate.

c)

The balanced reactions betweenI3- andHSO3- :

I3+HSO3+H2O3I+SO42+3H+

The balanced reactions between and thiosulfate

I3+2S2O32S4O62+3I

05

Step 5: The concentration of total sulfite in undiluted wine.

d)

The charge is:

q=lt=10103A240sq=2.4C

The mole of electron is:

ne=qF=2.4C96485C/molne=2.49105mol

The n ofI3-is:

nI3ne=12nI3=ne2=2.49105mol2nI3=1.24105mol

Now calculate of :

nS2O32=cS2O32VS2O32nS2O32=0.0507M0.5103LnS2O32=2.54105mol

The n ofI3 is:

nI3nS2O32=12nI3=nS2O322=2.54105mol2nI3=1.27105mol

The charge is:

q=lt=10103A131sq=1.31C

The mole of electron is:

ne=qF=1.31C96485C/molne=1.36105mol

The n ofI3- is:

nI3ne=12nI3=ne2=1.36105mol2nI3=6.79106mol

Now calculate how muchI3 is left,

nI3left=1.271056.79106molnI3left=5.91106mol

The sulfite in wine consumed:

n=1.241055.91106moln=6.49106mol

Because1moll3- reacts with mol sulfite, the wine contained6.49.10-6 mol sulfite in 2.00 mL the injected for analysis.

9.000 mLwine was diluted to 10.00mL .

So, the n of sulfite is:

n(sulfite)=1096.49106moln(sulfite)=7.21106mol

So, the concentration of sulfite is:

c(sulfite)=n(sulfite)Vinjectedn(sulfite)=7.21106mol2103Ln(sulfite)=3.61103moln(sulfite)=3.61mM

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with Vaia!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

How many hours are required for 0.100 mol of electrons to flow through a circuit if the current is 1.00 A?

Chemical oxygen demand by coulonetry. An electrochemical device incorporating photooxidation on a \({\rm{Ti}}{{\rm{O}}_2}\) surface could replace refluxing with \({{\rm{C}}_2}{\rm{O}}_7^{2 - }\) to measure chemical oxygen demand (Box 16-2). The diagram shows a working electrode beld at \( + 0.30\;{\rm{V}}\) versus \({\rm{Ag}}\mid {\rm{AgCl}}\) and coated with nanoparticles of 'TiO . Wltraviolet2inradiation generates electrons and holes in \({{\rm{T}}_1}{{\rm{O}}_2}\). Holes oxidize

organic matter at the surface. Electrons reduce \({{\rm{H}}_2}{\rm{O}}\) at the auxiliary electrode in a compartment connected to the working compartment by a salt bridge. The sample compartment is only 0.18 mm thick with a volume of \(13.5\mu \,{\rm{L}}\). It requires \(\~1\;\,{\rm{min}}\) for all organic matter to diffuse to the \({\rm{Ti}}{{\rm{O}}_2}\) surface and be exhaustively oxidized.

Left: Working electrode. Fight Photocument response for sample and blank Both solutions contain \(2{\rm{M}}\,{\rm{NaNO}}\). (Dst from H zhso, D. fisng. 5 . zhang K. Cutteral, and R. Jshn, "Development of a Drect Fhotselectrocherrical Method for Deterrination of Gherrical Ouygen Demand," And. Chan. 2004, 76 155.)

The blank curve in the graph shows the response when the sample compartment contains just electrolyte. Before inradiation, no current is observed. Ultraviolet radiation causes a spike in the current, followed by a decrease to a steady level near \(40\mu \). This current arises from oxidation of water at the \({\rm{Ti}}{{\rm{O}}_2}\)sufface under ultraviolet exposure. The upper curve sbows the same experiment, but with wastewater in the sample compartment. The increased current arises from oxidation of organic matter. When the organic matter is consumed, the cument decreases to the blank level. The area between the two curves tells us how many electrons flow from oxidation of organic matter in the sample.

  1. Balance the oxidation half-reaction that occurs in this cell:

\({{\rm{C}}_e}{{\rm{H}}_k}{{\rm{O}}_a}\;{{\rm{N}}_s}{{\rm{X}}_x} + {\rm{A}}{{\rm{H}}_2}{\rm{O}} \to {\rm{BC}}{{\rm{O}}_2} + {\rm{CX}} + {\rm{DN}}{{\rm{H}}_3} + {\rm{E}}{{\rm{H}}^ + } + {\rm{F}}{{\rm{e}}^ - }\)

where X is any halogen. Express the stoichiometry coefficients A, B, C, D, E, and F in terms of c, h, o, n, and x.

  1. How many molecules of \({{\rm{O}}_2}\)are required to balance the halfreaction in part (a) by reduction of oxygen (\({{\rm{O}}_2} + 4{{\rm{H}}^ + } + 4{{\rm{e}}^ - } \to 2{{\rm{H}}_2}{\rm{O}}\))?
  2. The area between the two curves in the graph is \(\int_0^\infty {({I_{{\rm{sample }}}}} - {I_{blank}})dt = 9.43\,{\rm{mC}}{\rm{.}}\) This is the number of electrons liberated by complete oxidation of the sample. How many moles of \({{\rm{O}}_2}\) would be required for the same oxidation?
  3. Chemical oxygen demand (COD) is expressed as mg of \({{\rm{O}}_2}\) required to oxidize 1 L of sample. Find the COD for this sample.
  4. If the only caidizable substance in the sample were \({{\rm{C}}_9}{{\rm{H}}_6}{\rm{N}}{{\rm{O}}_2}{\rm{CIB}}{{\rm{r}}_2}\). what is its concentration in molL?

Ions that react with Ag+can be determined electrogravimetrically by deposition on a silver working anode:

Ag(s)+X-AgX(s)+e-

(a) What will be the final mass of a silver anode used to electrolyze 75.00 mL of 0.02380 M KSCN if the initial mass of the anode is 12.4638 g?

(b) At what electrolysis voltage (versus S.C.E.) will AgBr(s) be deposited from 0.10M Br? (Consider negligible current flow, so that there is no ohmic potential, concentration polarization, or overpotential.)

(c) Is it theoretically possible to separate 99.99% of0.10M Klfrom0.10MKBr by controlled-potential electrolysis?

A monolayer (single layer of atoms) of Cuon the (100) crystal face shown in the margin has1.53×1015atoms/cm2=2.54×10-9mol/cm2. What current can deposit one layer of Cuatoms on1cm2in 1 s?

Ti3+ is to be generated in 0.10MHClO4 for coulometric reduction of azobenzene.

TiO2++2H++eTi3++H2OE0=0.100V4Ti3++C6H5N=NC6H5+4H2O2C6H5NH2+4TiO2++4H+

At the counter electrode, water is oxidized, and \(\mathrm{O}_{2}\) is liberated at a pressure of \(0.20\) bar. Both electrodes are made of smooth Pt, and each has a total surface area of 1.00cm2. The rate of reduction of the azobenzene is 25.9nmol/s , and the resistance of the solution between the generator electrodes is 52.4Ω.

  1. Calculate the current density (A/m2)at the electrode surface. Use Table 17-1 to estimate the overpotential for O2liberation.
  2. Calculate the cathode potential (versus S.H.E.) assuming that role="math" localid="1668356673323" [TiO2+surface]=[TiO2+]bulk=0.050Mand [Ti3+]surface=0.10M.
  3. Calculate the anode potential (versus S.H.E.).
  4. What should the applied voltage be?
See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.

Sign-up for free