Pipe Stem Trianglee Lab Report

2. Obtained a 2-3 cm strip of magnesium metal ribbon and coiled it loosely into a small ball. Added the magnesium metal to the acid in the test tube.

2. The second source of error in the lab is when opening the lid of the crucible which allowed smoke of magnesium oxide to escape. During the lab, we removed the lid a couple of times to allow oxygen to enter the crucible so the magnesium reacts with the air to form magnesium oxide. However, the smoke could have easily escaped from the crucible because of the strong force of heat from the laboratory burner. This could have affected the lab results by decreasing the final mass when some of the product have escaped.

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 first experiment is about the combustion of magnesium after which the ash is formed.

The purpose of this lab was to test the law of definite proportions for the synthesis reaction of combusting magnesium. In this lab, the polished magnesium ribbon was placed in covered crucible and was heated in order for it to react with Oxygen presented in air and in water provided. The result showed that Magnesium oxide formed through chemical reaction was made up of 60.19% magnesium and 39.81% oxygen, which is approximate proportion of both particles in every Magnesium oxide compound. From this lab it can be concluded that the law of definite proportion stating that the elements in a pure compound combine in definite proportion to each other is factual.

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 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

Subsequently, two porcelain crucibles were used, weighed, and heated for about 10 minutes and then placed into a desiccator to cool. The two empty porcelain crucibles were first heated because the heat would vaporize any impurities that were originally on the crucible. The first crucible weighed 11.9047 g and the second crucible weighed 12.3735 g. Once the mass of the two crucibles

As the acid was being added, the mixture was being stirred over a stir plate. Once completed, the reaction mixture was poured from the round bottom flask into a 500 mL separatory funnel and its top (organic) layer was extracted into another beaker. The bottom (aqueous) layer was placed back into the funnel and extracted twice with 50.0 mL of ethyl ether each. The newly extracted layers were combined and dried over magnesium sulfate (MgSO4). The dried solution was the decanted into a beaker to remove the MgSO4 salts and the product solution was collected via Buchner vacuum filtration. The resulting product was transferred into an Erlenmeyer flask with an inverted beaker on top and stored in a drawer.

5.3 mL of bromobenzne and 15 mL of anhydrous ether was then placed into the separatory funnel and was shaken and vented in order to mix the solution. Half of the bromobenzene solution was added first into the round bottom flask and as soon as a color change was observed, the remaining half of the bromobenzene was added drop wise into the round bottom flask. The mixture was then refluxed on a heating mantle for 10 minutes until most of the magnesium has been consumed.

One milliliter of 6.00-M phosphoric acid was placed into a 125-mL Erlenmeyer flask using a volumetric pipette. Using a slightly larger pipette, six milliliters of 3.00-M sodium hydroxide was transferred into a 50-mL beaker. Then a disposable pipette was used to slowly mix the sodium hydroxide into the phosphoric acid while the solution was swirled around. Then both the beaker and flask were rinsed with 2-mL of deionized water and set aside. A clean and dry evaporating dish was weighed with watch glass on a scale. Then the solution was poured into the dish and the watch glass was placed on top. The solution was then heated with a Bunsen burner to allow for the water to boil off to reveal a dry white solid. After the dish cooled to room temperature it was once again weighed and the new mass was recorded.

Figure 1: Line graph plotting the mean changes of blood glucose concentrations recorded (mmol/L) over timed intervals (30 min) spanning the duration of the two-hour experiment. As the associated figure legend indicates, the red line is the resulting change in mean blood glucose concentration in response to individuals undergoing the ‘Glucose Rest’ experimental condition. The blue line is a recording of the mean capacity for individuals to dispose of glucose load when required to exercise (Glucose Exercise condition). As an extension of the glucose tolerance test, the green line is a mean plot of how fructose consumption affects blood glucose concentrations. The last experimental group ‘Glucose Sip and Spit’ in orange, displays how to consumption or rather lack of glucose, affects one’s ability to dispose of glucose load, hence affecting the blood glucose concentrations (mmol/L).

To calculate the expected number of pipette tips needed per month take the number of pipette tip per sample to multiply it with the average sample analysed per month, 5 x 100 = 500.

In most of the world planes, spaceships and helicopters have been tested in wind tunnel. The wind tunnel is a chamber where the high speed air is passed through. The objective of this experiment is to determine the velocity profile at a single location within the wind tunnel by using the Pitot tube. Firstly, make plot of the non-dimensional distance Versus non-dimensional velocity to compare the plot with White’s Figure 7.5. Then Reynolds number, coefficient of drag, skin friction coefficient, free stream velocity and boundary layer thickness should to be determined.