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

Short Answer

Expert verified

Starch is added just before the end point in iodometry technique when the I3-starts to fade. It is not added at the beginning of the technique because some of I2 would stay bounded to starch and the end point would not be detected right.

Step by step solution

01

Definition of Iodometry.

  • Iodometry, regularly called iodometric titration, is a redox titration approach wherein the emergence or disappearance of essential iodine determines the cease point.
  • In iodometry iodide is added to a solution of an oxidizing agent. The iodide is oxidized to iodine. The iodine is titrated with sodium thiosulfate for quantitative analysis.
  • In iodimetry, the titration is done with iodine solution.
02

Determine the technique that used starch indicator not added until the end point.

  • Starch is added just before the end point in iodometry when the I3-starts to fade.
  • It is not added at the beginning of the technique because some of would stay bounded to starch and the end point would not be detected right.
  • A starch solution is used as an indicator in an iodometric titration because it can absorb the I3that is emitted.
  • When titrated with standardised thiosulfate solution, this absorption causes the solution's colour to change from deep blue to pale yellow.
  • This represents the titration's termination point.
  • Iodometry is a technique for determining the quantity of oxidising chemicals in water samples, such as oxygen saturation in ecological research or active chlorine in pool water analysis.

Hence, starch is added before the end point in iodometry technique.

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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.

Iodometric analysis of high-temperature superconductor. The procedure in Box16 - 3 was carried out to find the effective copper oxidation state, and therefore the number of oxygen atoms, in the formula YBa2Cu3O7, where 0z0.5.

(a) In Experiment A of Box 16 - 3, 1.00 g of superconductor required 4.55 mmol of role="math" localid="1654948290716" S2O32-. In Experiment B,1.00 g of superconductor required 5.68 mmol ofS2O32- Calculate the value of z in the formula YBa2Cu3O7-z(FM ).

(b) Propagation of uncertainty. In several replications of Experiment A, the thiosulfate required was 4.55(±0.010)mmol of role="math" localid="1654948278531" S2O32- per gram of YBa2Cu3O7. In ExperimentB, the thiosulfate required was 5.68(±0.05)mmol of S2O32-per gram. Calculate the uncertainty x of in the formulaYBa2Cu3Ox.

Why is iodine almost always used in a solution containing excess l-?

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?

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(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.

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.

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