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Separating homogeneous mixtures
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The Objective The purpose of this experiment was to learn and preform an acid-base extraction technique to separate organic compounds successfully and obtaining amounts of each component in the mixture. In this experiment, the separation will be done by separatory funnel preforming on two liquids that are immiscible from two layers when added together. The individual components of Phensuprin (Acetylsalicylic acid, Acetanilide, and Sucrose as a filler) was separated based upon their solubility and reactivity, and the amount of each component in the mixture was obtained. Also, the purity of each component will be determined by the melting point of the component. Structures/Reactions/Properties Substance Structure M. F. M.W. m.p. (c) b.p(c) Density …show more content…
The mixture was poured through a weight filter paper and Sucrose washed with a 5ml of dichloromethane. The resulting solid was left in a breaker to dry for one week, to be measured. Left it in the drawer to dry out for a week and weighted it to find the sucrose amount recovered amount. - Fluted paper weight: 0.98 - Fluted paper weight + Sucrose weight: 1.416 - Sucrose weight: 1.416 - 0.98 = 0.436 g - Melting point range of Sucrose: 190 C – 169 C = 21 C Isolating the Acetylsalicylic …show more content…
Extraction is a separation method that is often used in the laboratory to separate one or more components from a mixture. Sucrose was separated at the beginning because it is the most immiscible and it’s strongly insoluble. Next Acetylsalicylic Acid was separated which left Acetanilide alone. Variety steps could have led to errors occurring. For example the step of separation, when dichloromethane layer was supposed to be drained out, it could be possible some aqueous layer was drained with it. Which could make the end result not as accurate. Also errors could have occurred if possibly some dichloromethane was not drained out. Both way could interfere with end result of figuring the amount of each component in the mixture. The solids percentage were 22.1% more than the original. That suggests that solids weren’t separated completely which clarifies the reason the melting points that were recorded were a slightly lower than the actual component’s melting point. The melting point for Acetylsalicylic Acid is 136 C but that range that was recorded during the experiment was around 105 C to 118 C. The melting points were slightly lower than the literature value. Sucrose was the purest among all component due to its higher melting point which follows the chemical rule that the higher the melting point the more pure the component
A: The reaction with water and vinegar was the most useful in this experiment. The physical properties were very self explanatory because the texture of the powders was all different expect icing sugar and cornstarch. Also the Ph levels were very similar of six and seven for corn starch and icing sugar respectively. d) Q: How confident do you feel about your identification of the
Once the mixture had been completely dissolved, the solution was transferred to a separatory funnel. The solution was then extracted twice using 5.0 mL of 1 M
It could have been lower than 100% because some product was lost during the recrystallization process, or due to an incorrect separation of the impurities when cooling the mixtures. The melting point data confirmed that the synthesized crystals were likely identical to the methoxybenzyl phenol ether because the mixed melting point was the same as the purified crystals. If the products were different or the synthesized product had to many impurities in it then the mixed melting point would have been lower than that of just the crystals, by themselves. The TLC made sense, after looking at the TLC plates under UV light and the calculation of the Rf values, it was confirmed that the 4- Methoxy-phenol was present in the unknown.
The objective of this experiment was to perform extraction. This is a separation and purification technique, based on different solubility of compounds in immiscible solvent mixtures. Extraction is conducted by shaking the solution with the solvent, until two layers are formed. One layer can then be separated from the other. If the separation does not happen in one try, multiple attempts may be needed.
Repeat for each trial. Rinse volumetric pipette with vinegar and drain into the waste beaker. Weigh and record the mass of each 200mL beaker. Add 10.00mL of vinegar into each beaker and weigh them and record their again. Add 50mL of de-ionized water to the beakers and place them under the drop counter on top of a stir plate, submerging the pH meter into the solution. Place the stir bar into the beaker and carefully turn on the stir plate so that the stir bar spins without splashing or hitting the sides of the beaker or the pH
The aspirin crystals were packed into 3 small capillary tubes to ensure that they are compressed so as to prevent any air gaps. Subsequently, the aspirin crystals that are in the 3 capillary tubes are placed into the melting apparatus and the temperature range was recorded. Since the range is quite far from the theoretical value of 140°C, aspirin's purity attained was low due to impurities present. One potential reason is because of the swift cooling. When the aspirin is left to cool, the crystal lattices will form too rapidly which will surround other molecules thus making the aspirin impure. Another reason could be because the recrystallized aspirin has not dry completely and there might me left over solvent that will affect the temperature range of the aspirin.
== Refer to, Chemistry Lab #1 – What’s the substance? I didn’t change most materials when I did this experiment, but I added 4 materials, which are: * 5 test tubes * 2 stoppers * 1 large piece of paper And I deleted 1 material, which is: * Spatula Methods = == ==
...r 15minutes. I would keep the method the same as I did doing this investigation but try a salt solution instead of sucrose as it would be easier to make different concentrations by having a certain amount of salt per 100cm³ of distilled water.
The conical vial was placed in a small beaker and allowed to cool to room temperature. The mixture was Cooled thoroughly in an ice bath for 15-20 minutes and crystals collected by vacuum filtration on a Hirsch funnel. The vial was rinsed with about 5 mL of ice water and transferred into to the Hirsch funnel and again washed with two additional 5mL portions of ice water. Crystals were dried for 5-10 minutes by allowing air to be drawn through them while they remained on the Hirsch funnel. The product was transferred to a watch glass plate and allow the crystals to dry in air. Crude acetaminophen product was weighed and set aside a small sample for a melting point determination and a color comparison after the next step. Calculation of the percentage yield of crude acetaminophen (MW = 151.2). was done and recorded in the lab notebook.
If the solid dissolved in the solvent at room temperature, then it was too soluble and that solvent could be eliminated. The acetanilide is completely dissolved in ethanol and dichloromethane, therefore eliminating them from being the suitable solvent. If the solid did not dissolve at room temperature then it was placed in the sand bath and left to boil. If the solid dissolved, it was placed in the ice bath and if crystals were observed coming out of the solution then the suitable solvent was found. The suitable solvent was water as the crystals came out once placed in the ice bath.
10% - 15%. I intend to place a predefined weight of potato cells (0.15g) in varying concentrations of sucrose solution (0%, 20%, 40%, 60%, 80%), to see the effects of osmosis in the cells of a potato in varying levels of sucrose solution. The potato cores will be prepared, weighed and then placed in the solution and left for a certain amount of time, they will then be removed, re-weighed and the difference in weights calc...
This paper describes the separation and isolation of the three active components of Excedrin. The three components of aspirin, acetaminophen, and caffeine were separated using the technique of acid-base extraction with K2HPO4 and KOH being the bases and HCl as the acid. Distillation was also performed on the ether layer to extract the caffeine. One week later, crystals from the K2HPO4 and KOH solutions were acquired via vacuum filtration. Due to the ether evaporating, crystals from the ether did not need to be filtered. Thin Layer Chromatography (TLC) was then performed on the K2HPO4 crystals, the KOH crystals, the ether crystals, the K2HPO4 liquid solution, and the KOH solution. The TLC determined the K2HPO4 crystals as aspirin, the KOH crystals
Analysis of Aspirin Tablets Aim --- To discover the percentage of acetylsalicylic acid in a sample of aspirin tablets. ----------------------------------------------------------------- In order to do this, the amount of moles that react with the sodium hydroxide must be known. This is achieved by using the method of back titration.
We predicted that by using the titration formula the concentration of acetic acid in vinegar can be determined by using 1 M HCl and a solution of NaOH of an unknown concentration because titration finds the concentration of an unknown solution by using the concentration of a known solution (Bronx Science. Experiment 2.12: Acid-Base Titration Lab. 2016). By using the solution of NaOH of unknown concentration with 0.1 M HCl, the concentration of acetic acid in vinegar can be calculated. After the NaOH was standardized, using the titration formula, the concentration of acetic acid in vinegar was found to be .100 M
Part A of the experiment, we were measuring the density of water. In this part, we measured by difference by measuring the mass of the empty graduated cylinder which was 46.35 grams and then added 25.0 milliliters of water to it. When subtracting by difference, our mass of the water was 25.85 grams. This was close to the measurements of the water added to the graduated cylinder. The density of the water was 1.0 grams/milliliters.