Determining the Number of Moles of Water of Crystallization Associated With One Mole of Copper (II) Sulfate in a Hydrate CuSO4 * xH2O (s).

The purpose of this lab is to determine the formula of an unknown hydrate. To achieve this, we heated a hydrate over a Bunsen burner to drive out the water. As a result, the anhydrate is left and the data is used to calculate the mole ratio between the amount of anhydride and water. Then the mole ratios are used to calculate the hydration number, which was 4.8, but was rounded to 5 in the formula. The accepted formula is 〖CuSO〗_4∙5H_2 O and the percent of error was 4%.

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.

As a group, we obtained our salt mixture of calcium chloride and potassium oxalate, and weighed the mixture. We were able to make an aqueous solution from the mixture and distilled water. We boiled and filtered off the solution, leaving the precipitate. Once the precipitate was dried overnight, it was weighed and the mass was measured. Then we calculated the moles of the precipitate.

Materials:Magnesium stripCrucibleCrucible coverClay triangleIron ringRetort standTongsBalanceBunsen burnerProcedure:1.obtained a strip of magnesium between 30-40 cm long2.coiled magnesium strip into a tight roll3.measured the mass of the crucible and cover4.Added the magnesium strip to the crucible and measured the

The purpose of this experiment was to determine the percent by mass in a hydrated salt, as well as to learn to handle laboratory apparatus without touching it. The hydrated salt, calcium carbonate, was heated with high temperature to release water molecules. Gravimetric analysis was used in this experiment to determine the percent by mass of water in a hydrated salt. The hypothesis of this experiment was accepted on the basis that the percent by mass of volatile water in the hydrated salt would be fewer than 30%. The percent by mass was determined by the mass of water loss devised by the mass of hydrated salt multiplied by total capacity

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.

Then 8.0g of copper sulfate crystals were placed inside the beaker and the mass was recorded for the actual crystals. 50 mL of water was added to the beaker with the crystals. The ring stand was set up with the wire mesh on it and one partner should place the mixture in the beaker on it should be heated without letting the mixture boil. Stir the mixture and heat until the crystals are dissolved. While one partner does this, the other should obtain 1.5g of iron filings in a measuring cup and records the mass. Then the iron filings should be added small amounts at a time to the heated solution. Stir continuously until all the mixture is added to the beaker. Then it sat for 10 minutes and observations were recorded. Record the mass of a filter paper and set up a filtration apparatus with the filter paper in a funnel over an Erlenmeyer flask. Decant the liquid through the paper slowly trying not to allow any solid to get on the filter paper. Then with de-ionized water, rinse your solid in the beaker and let the solid settle then decant the liquid. Repeat the washing twice more and in the last time guide all the solid into the filter paper. Then place the filter paper on a watch glass and then into a warm oven to dry. After it is cool, record the mass of the watch glass, filter paper and solid. If there is not enough time to cool, you may have to do it the next

The mass percent of water was determined using the mass of water and dividing it by the total mass of the hydrate and then multiplying that answer by 100%. The number of moles of water in a hydrate was determined by taking the mass of the water released and dividing it by the molar mass of water. The number of moles of water and the number of moles of the hydrate was used to calculate the ratio of moles of water to moles of the sample. This ratio was then used to write the new and balanced equation of the dehydration process. The sample was then rehydrated to the original state and the percent of the hydrate recovered was calculated by using the mass of the rehydrated sample by

The purpose of this lab is to determine the percent of water in a hydrate. I learned that copper sulfate hydrate is blue on its own but, when heat is added it will change color to a dim gray. One error that may have occurred is the failure to zero the scale which would ultimately change the math in the equation. Another error that may occur in this lab is forgetting to wait the recommended amount of cooling time, which would change the mass of the elements. At the end if the lab when we look to the questions, it is also beneficial to look at the notes for the lab because it helps with the setup of equations that may come with the questions, also it is very helpful

The goal of this experiment was to determine the empirical formula for a hydrate of magnesium sulfate and water. The technique that was used was measure the mass of the hydrate and then apply heat to evaporate the water. Then determine the mass of water that was in the hydrate and the mass of the remaining magnesium sulfate. The equation for the hydrate is determined by calculating the mole to mole ratio of the water and the anhydrous. The resulting formula will be formated as: MgSO4*_H2O

The powdered cobalt oxalate hydrate was weighed to about 0.3 g and placed in a pre-weighed crucible. The crucible and the cobalt oxalate were then heated until the cobalt oxalate decomposed into a stable, black solid, or Co3O4. Once the crucible was sufficiently

During the heating period, a noticeable change took place in the sugar test tube – it began to caramelize, melting into a golden brown color, then finally a dark brownish/black hue; it remained constant at that color. The copper sulfate began losing color when applied to the heat, turning from a bright blue to white and remained white after heating. Once cooled, 2-3 drops of water were added to each tube; the sugar remained the same, while the copper sulfate immediately bubbled and transformed from white back to its original blue hue. Next 1-3 grams of the hydrated copper sulfate were added to a crucible, which was weighed prior to adding the sample, then heated gently with a Bunsen burner. Once the salt stopped changing color, it was heated for an additional 5 minutes, then the total mass was measured. Finally, a pea-sized amount of Epsom Salt was added to a test tube and heated for 1 minute without the tube becoming red

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:-

Assign one member of the group to gently stir solution with a thermometer (See figure 2)

In this experiment, the Ksp for calcium sulfate dihydrate, CaSO4·2H2O, by titrating 4 times a calcium sulfate dihydrate solution with diprotic EDTA, H2(EDTA)2-. For each trial we found the Ksp by means of molarities and activities. The results for the Ksp using only molarities was very different than the Ksp using activities. The average Ksp using molarity only was 2.26 x 10-4 and the average Ksp using activity turned out to be 2.31 x 10-5. The actual Ksp however, is 3.14 x 10-5. A percent error of 26.6 % was calculated.