Chapter 16: Q22P (page 392)
Why is iodine almost always used in a solution containing excess ?
Short Answer
Iodine is always used in a solution with excess because pure is not a polar substance and it cannot be dissolved in water.
Chapter 16: Q22P (page 392)
Why is iodine almost always used in a solution containing excess ?
Iodine is always used in a solution with excess because pure is not a polar substance and it cannot be dissolved in water.
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Get started for freeConsider the titration of 25.0mL of 0.0500MSn2+with 0.100MFe3+in 1MHCI to give Fe2+ and Sn4+, using Pt and calomel electrodes.
(a) Write a balanced titration reaction.
(b) Write two half-reactions for the indicator electrode.
(c) Write two Nernst equations for the cell voltage.
(d) Calculateat E the following volumes of Fe3+: 1.0,12.5,24.0,25.0,26.0 and 30.0mL. Sketch the titration curve.
Calcium fluorapatitelaser crystals were doped with chromium to improve their efficiency. It was suspected that the chromium could be in theoxidation state.
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2. In a second step, the total chromium content was measured by dissolving a crystal in at and cooling to . Excess and were then added to oxidize all chromium to . Unreacted was destroyed by boiling, and the remaining solution was titrated with standard . In this step, each Crin the original unknown reacts with three .
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.
Whenof unknown were passed through a Jones reductor, molybdate ion was converted into . The filtrate required 16.43mLof to reach the purple end point.
A blank required 0.04mL. Balance the reaction and find the molarity of Molybdate in the unknown.
Why don'tand interfere in the analysis of when a Walden reductor, instead of a Jones reductor, is used for pre-reduction?
Would indigo tetrasulfonate be a suitable redox indicator for the titration of with in 1MHCI? (Hint: The potential at the equivalence point must be between the potentials for each redox couple.)
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