Copper Iodide Synthesis Lab Report

This experiment is based on determining the chemical formula for a hydrated compound containing copper, chloride, and water molecules in the crystal structure of the solid compound, using law of definite proportion. The general formula of the compound is CuxCly•zH2O, and aim is to determine chemical formula of this compound.

Before placing the Aluminum foil into the Copper Chloride Water (CuCl2 + H2O), I had examined the characteristics of the aluminum foil. It came to view that the Aluminum foil was a silver-coloured, shiny metal. When the aluminum foil was placed into the CuCl2 Water solution, several observations were made.

In this task the concentration of an unknown sample of copper sulphate using colorimetry was used to find the concentration. In this investigation copper sulphate was used which is CuSO4.5H20 as a formula. To make a standard solution which was 1M, the same clean equipment was used to make up the standard solution as used to make sodium carbonate. However there was one difference and that was that the hot distilled water was used to dissolve the copper sulphate crystals. There had to be enough hot water in order to dissolve the crystals into the beaker and then add cold distilled water to cool the solution.

The purpose of the experiment is to cycle solid copper through a series of five reactions. At different stages of the cycle, copper was present in different forms. First reaction involves reaction between the copper and nitric acid, and copper changed from elemental state to an aqueous. The second reaction converted the aqueous Cu2+ into the solid copper (2) hydroxide. In the third reaction Cu(OH)2 decomposed into copper 2 oxide and water when heated. When solid CuO reacted with sulfuric acid, the copper returned to solution as an ion (Cu2+). The cycle of reactions was completed with the reaction where elemental copper was regenerated by Zn and Cu

The purpose of performing the variety of tests that we did was to give more accurate results of what the unknown mineral was. By roasting the copper mineral, we obtained copper(II) oxide. This new sample came out of the crucible grayish-black. It was very brittle and full of cracks. This provided the percent composition that was necessary in finding the unknown mineral. When performing

For our science assessment we had the task to research about a metal of our choice. Since I am really into computers, I chose copper. A metal used in all kinds of wires, cpu’s and other stuff without a computer wouldn’t work. This fits really well into what we have to do for the second part, describe how this metal has helped human society.

Put approximately 9-10(g) copper ore into beaker. Use spatula to break up any large pieces. Next add 17ml H2SO4 (aq) (hydro sulfuric acid) to the beaker. Began mixing until all or most traces of blue dissipate; or the copper ore will no longer dissolve (should appear as a milky liquid). Next use pipette to and remove solution and divide solution into 2 individual test tubes then Place test tubes into centrifuge and run centrifuge for 1 minute. Remove from centrifuge machine Fill a cuvette with the clear solution from the test tube making sure not to disturb the sediment at the bottom. Note the solution should bluish in tint Final place the cuvette in the colorimeter. Then record data and calculate in results section.

XIII. Carefully remove the copper metal from the filter paper onto the watch glass. (with a spatula) Place a 400 ml beaker on a hot plate contained with water. Carefully place the watch glass before the water boils to dry the copper metal. (Use the tongs to handle the hot watch glass)

Purpose: The purpose of this experiment was to observe the many physical and chemical properties of copper as it undergoes a series of chemical reactions. Throughout this process, one would also need to acknowledge that even though the law of conservation of matter/mass suggests that one should expect to recover the same amount of copper as one started with, inevitable sources of error alter the results and produce different outcomes. The possible sources of error that led to a gain or loss in copper are demonstrated in the calculation of percent yield (percent yield= (actual yield/theoretical yield) x 100.

The lab performed required the use of quantitative and analytical analysis along with limiting reagent analysis. The reaction of Copper (II) Sulfate, CuSO4, mass of 7.0015g with 2.0095g Fe or iron powder produced a solid precipitate of copper while the solution remained the blue color. Through this the appropriate reaction had to be determined out of the two possibilities. Through the use of a vacuum filtration system the mass of Cu was found to be 2.1726g which meant that through limiting reagent analysis Fe was determined to be the limiting reagent and the chemical reaction was determined to be as following:-

Wash a crucible and cover. Heat in the coolest part of the flame for 3 minutes to dry. Allow to cool, then measure and record the mass of the crucible and cover in the data table.

My fourth report will be on the medical use of iodine. I will specifically focus on Iodine as a sterilization agent for surgeries or wounds in health care. Iodine is a chemical element used often in disinfectant found in the OR suite of a hospital.

The reaction characteristics of basic copper carbonate 〖mCuCO〗_3⋅n〖Cu(OH)〗_2 were observed by changing the reaction mole ratio. The reaction mole ratio of sodium carbonate to copper chloride (II) was controlled from 1.08 to 1.68. Fig. 1 shows the XRD patterns of copper carbonate powder. At a reaction ratio of 1.08, paratacamite (Cu_2 Cl(OH)_3 ), beside alkali copper carbonate, was formed because of incomplete reaction at a copper content of 53.9 wt%. Lack of sodium carbonate may cause incomplete reaction with copper chloride (II) because of low pH (6.0) of the solution [12]. The copper content according to the reaction mole ratio were 57.7, 50.5, 58.8, 59.3, and 59.8 wt% at the reaction mole ratios of 1.20, 1.32, 1.44, 1.56, and 1.68, respectively.

Solutions of CuSO45H2O (0.506 g in 10mL water, 3.17E-3 mol) and ammonium peroxodisulfate (1.030 g in 10mL water, 4.51E-3 mol) were prepared and mixed

When the zinc was added to the copper (II) sulfate solution, the solution started to bubble. As the solution was stirred, it turned a cloudy blue. Small flecks of a brown solid were visible. As the solution became colorless, the brown solid settled to the bottom of the beaker. The solid formed was copper in its elemental state. The color faded from the solution as the copper ions slowly formed into solid copper. The copper was poured into a funnel with filter paper and washed three times with 25 mL