Percent Recovery was calculated by taking the total amount of grams collected and dividing it by the amount of grams initially started with and multiplying that number by 100.
Phthalic Acid: (.15g / .20g) * 100 = 75%
Benzoic Acid (Water): (.03g / .05g) * 100 = 60%
Benzoic Acid (Methanol): (035g / .05g) * 100 = 70%
Naphthalene: (.532g / 1g) * 100 = 53%
Discussion
After the process of recrystallization was completed, the melting points and weights were taken for each solid. Some melting points recorded for the solids were very close to the values listed in the literature. However, others differed by sizeable margins from the values listed in the literature. The range observed for the melting point of naphthalene was 78-81°C. This coincides with
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The text suggested that the solvent be removed by evaporation via a hot water bath or filtration (Weldegrima 2016). A situation occurred during the lab where time had become a constraint and the hot water bath was being occupied by the naphthalene. The instructor advised that the sand bath be used to isolate the crystals from the solvent, or the crystals and liquid be poured on filter paper and hand dried. The sand bath was too hot and started to melt the solid. This led to the pouring of the liquid and crystals onto filter paper. This method left more room for error, as drying the crystals would be more tedious and it would be more difficult to remove all the crystals from the test tubes. The optimal percent recovery is a 100% for each solid. However, it is expected that less would be obtained. The percent recovery for the benzoic acid in both procedures and the phthalic acid were between 40%-25% less than the desired 100%. The low percent recovery can be attributed to the method previously mentioned, to separate the solvent from the crystals. When pouring the crystals and liquid onto the filter paper for the benzoic and phthalic acid, it could clearly be seen that there were many crystals still stuck to the inside of the tube. A spatula was used to recover as much of the crystals as possible, but not all of the crystals could be collected. This left many crystals still in the test tube which would have skewed the results for percent recovery, as they could not be weighed as well. The naphthalene was different, as it was not pure to begin with. A 1g solid mixture including an unknown amount of naphthalene was used. The lack of information on how much naphthalene was started with, makes it very cumbersome to determine the percent yield. However, .532g of naphthalene was recovered in total. There
The melting point of the final product, diphenylacetylene, was found to be 65-68 degrees Celsius which is right around the ideal 61 degrees Celsius melting point; this shows that purification during the lab worked and that the sample was almost 100% pure. Since only 0.01g of diphenylacetylene was collected and the theoretical yield was calculated to be 0.049g, this experiment had a 20.41% yield. A few sources of error that explain the low percentage could be the loss of crystals when transferred from the test tube to the suction apparatus or when they were transferred from the suction apparatus to the filter paper to be dried and then weighed. Crystals could have also been lost if more than 5 drops of methanol was added because excess methanol would dissolve the crystals. The experiment was successful when looking at the crystals collected from the addition step and the elimination step; however, to improve the percent yield and collected product the the test tubes could have been allowed to cool down in the ice bath past the 5 minutes to ensure all the crystals formed
1. Our percent yield for alcohol was 84.2% which is average. We rushed through our vacuum filtration and probably did not let the solid dry long enough and might have not transferred all of the solid to the vacuum filtration from the beaker.
A buffer is a solution that resists changes in pH when H+, OH-, or H20 is added. By using standard lab equipment, a lab pro diagnostic tool, and acidic and basic solutions, the pH can be found. By recording the pH while adding a base or an acid gradually to a buffer solution you can find the capacity of each buffer to resist drastic changes in pH. The best buffers will keep a solution from becoming either too acidic or basic with the addition of a strong base or acid.
The objectives in this laboratory were to be able to calculate the freezing point depression among three trials of unknowns, be able to correctly measure the freezing points of p-xylene, and to be able to calculate the molar masses of the unknowns by found freezing point depression values. This was done to be able to understand and apply a concept names supercooling. Supercooling is when a liquid is put far under its original freezing point and remains a liquid or gas. This happens when a substance is cooled so quickly that it’s easier for it to stay a liquid than to crystalize, until it reached its nucleation point and begins to heat up returning to its freezing point (image 4). The supercooling of p-xylene was observed in three
The mixture was transferred to an ice bath to crystallize the product, after which the product was collected by vacuum filtration on a Hirsch funnel, washing the flask with small aliquots of cold xylene and pouring the solution over the crystals, allowing the vacuum to thoroughly dry the product. Additional drying was achieved by transferring the product to filter paper and pressing the crystals to remove any excess moisture. The product was then weighed and a melting point determined. A comparative TLC was run in Hexanes:Ethyl Acetate solvent against maleic anhydride to verify the purity of the
Discussion: As seen in the melting point determination, the average melting point range of the product was 172.2-185.3ºC. The melting points of the possible products are listed as 101ºC for o-methoxybenzoic acid, 110ºC for m- methoxybenzoic acid, and 185ºC for p- methoxybenzoic acid. As the melting point of the sample
Three grams of a mixture containing Benzoic Acid and Naphthalene was obtained and placed in 100 ml beaker and added 30 ml of ethyl acetate for dissolving the mixture. A small amount (1-2 drops) of this mixture was separated into a test tube. This test tube was covered and labelled as “M” (mixture). This was set to the side and used the following week for the second part of lab. The content in the beaker was then transferred into separatory funnel. 10 ml of 1 M NaOH added to the content and placed the stopper in the funnel. In the hood separatory funnel was gently shaken for approximately one minute and vent the air out for five seconds. We repeated the same process in the same manner one more time by adding 10ml of 1M NaOH.
In this lab, liquid-liquid extraction was performed to isolate a mixture of benzocaine and benzoic acid. 2.0107 grams of the mixture was first weighed out for the trials. When HCl was added to the mixture for the first acid extraction of benzocaine, an emulsion formed during inversion and venting that prevented a defined separation of the two layers. 8 mL of water was therefore added before continuing the extraction. The addition of NaOH then turned the top aqueous layer basic, indicated by the pH strips that turned blue when tested. A vacuum filtration isolated 0.29 grams of benzocaine and a MelTemp apparatus measured the crystal’s melting point ranges to be 85.1C-87.4C. For the base extraction of benzoic acid, the aqueous layers were retrieved
2-naphthol has a molecular weight of 144.17 g/mol, with a density of 1.22 g/cm3. The melting point of 2-naphthol is in the range of 121 to 123 °C. The stock solution of 2-naphthol has a concentration of 1.9844E-3 M.
The purpose of this experiment is to investigate the recovery time of the heart rate for teenagers according to various levels of exercise.
The purpose of this experiment is to separate a mixture of salicylic acid and naphthalene using extraction, recrystallization and sublimation techniques. Extraction is the separation of compounds from a mixture based on their relative solubilities in different solvents. Sublimation is the process of separation by which a substance transitions from the solid phase into the gas phase, skipping the liquid phase. Recrystallization involves dissolving a substance in an appropriate solvent then crystallizing it as it cools (impurities remain in solution). The melting points of the substances were determined in order to assess their purity and the percent recovery of pure naphthalene and salicylic acid were calculated. According to the results, the melting point of pure naphthalene was between 86°C -89°C range, whereas for pure salicylic acid was 167°C -170°C. Both determined melting points were higher compared to the literature value of 80.26°C and 158.6°C for pure naphthalene and salicylic acid respectively. Lastly, the percent recovery for pure naphthalene and salicylic acid were 17.7% and 71.2% accordingly.
The objectives of this lab are, as follows; to understand what occurs at the molecular level when a substance melts; to understand the primary purpose of melting point data; to demonstrate the technique for obtaining the melting point of an organic substance; and to explain the effect of impurities on the melting point of a substance. Through the experimentation of three substances, tetracosane, 1-tetradecanol and a mixture of the two, observations can be made in reference to melting point concerning polarity, molecular weight and purity of the substance. When comparing the two substances, it is evident that heavy molecule weight of tetracosane allowed
2. (5 pts) List and explain the names and affiliations of the various characters/stakeholders in this story – I’m looking for us to use the story to map out the complexities that are generally associated with solving public health puzzles – the stakeholders you list and explain here should apply to many of the cases we consider going forward.
To apply thermal analysis to the two-component system, naphthalene-biphenyl at atmospheric temperature. The analysis will be represented by a solid-liquid phase diagram (freezing point diagram).
Recrystallization was done to remove impurities from the sample. The percent recovery of benzoic acid during recrystallization is 23.02%. The difference between the pure and impure samples was observed by comparison of melting points. It was found that impure sample had a lower and wider melting point range of 120.1-122.2 (C). The pure sample melting point range was 121.3-122.5 (C). These ranges helped determine purity by comparing the known melting point of pure benzoic acid.