Synthesis of aspirin lab

At the same time place the mL beaker containing 70 mL DI water in the second ice bath set up previously for 20 minutes. As early as BC ancient cultures such as Greek, Roman, Egyptian, and Chinese found that extracts from plants such as willow bark, meadowsweet, and myrtle possessed the ability to alleviate fever, pain, and inflammation.

To do this, place an arbitrary amount of the substance to be weighed greater than the desired amount on the Fischer balance and press the tare bar to reset the balance Synthesis of aspirin lab zero.

This initial crystallization can be induced by scratching the side of the beaker: Today aspirin, also known as acetylsalicylic acid, is an over the counter medication that is extremely popular and is used for relieving pain, reducing fever, reducing swelling, and slowing blood clotting.

In this part, purification is not yet complete it was continued on the recrystallization part. Since this esterification reaction is not spontaneous, sulfuric acid was used as a catalyst to initiate the reaction.

Synthesis and Characterization of Aspirin

To purify the crude product, water was added to solution to further lower the solubility of acetylsalicylic acid and to dissolve some of the impurities from the crystal.

Certainly, another error occurred. Many intermediary steps happen in between the first and last steps, however. Catalysts do not change the composition of the final product, however, and this is also visible in Figure 2.

Synthesis of Aspirin Lab Report

The first of these is the concept of a limiting reactant. The melting point of the purified product was lower than the expected degree Celsius melting point of aspirin, which revealed to us that the purified aspirin product still contained some impurities.

Percent yield problems allow us to calculate what percent of the expected product we are able to account for by the end of our experiment. Purification is needed to eliminate any salicylic acid and acetic anhydride that did not react, as well as the acetic acid product and phosphoric acid.

Synthesis and Characterization of Aspirin

Clean and dry any glassware used and return it to the appropriate location. The third test tube labeled C is a control. Heat the 25 mL Erlenmeyer flask in a water bath not to exceed 50 degrees Celsius until all of the product has dissolved. The second part of the experiment was recrystallization.

The weight of the recovered sample was 2. A catalyst is something that changes the rate of a reaction, but is not actually consumed in the reaction itself. Phosphoric acid was used as a catalyst.

Mechanism of Reaction Many intermediate steps occur in the reaction Salicylates have a long history of use to alleviate aches and pain. The need for the strong conjugate base is the reason why other strong acids such as HCl is not used since its conjugate base Cl- is very weak compared to HSO When liquid is placed in a narrow vertical glass tube, the forces of adhesion and cohesion will cause to form a curve in the tube.

Turning the aspirator on will cause a low-pressure area in the vacuum hose, which will in turn pull air and anything else through the crucible that can get through the filter liquid. The process of vacuum filtration uses a filter crucible, an aspirator, and a vacuum hose in order to separate a liquid from a solid.

It is possible to repeat this process in order to end up with the desired amount of substance in the end. The mechanism of the reaction is: Calculate the percent yield of the product formed.

By observing the substance and noting at which temperature the substance starts to melt then what the temperature the substance is completely melted, it is then possible to determine the range of the melting point.

The mass of the crude aspirin product was 4. By measuring the melting point of the synthesized substance as well as taking a UV spectroscopy, it is then possible to measure the purity of the synthesized compound as well.

Cold water, on the other hand, is used to recrystallize only aspirin, thus, leaving all the impurities behind. Reaction Reaction of Salicylic Acid and Acetic Anhydride to form Aspirin and Acetic Acid The rings shown in the Salicylic acid and Aspirin molecules are hexagonal rings of carbon compounds, with alternating single and double bonds as indicated by the double lines.

The aspirin product that was collected still contained some impurities.Lab 1: Synthesis of Aspirin Introduction: The purpose of this lab was to demonstrate the ability to easily alter the molecular structure of a compound to greatly increase its utility. In this case, an acetyl group was added to salicylic acid, a naturally occurring compound with significant pharmaceutical value.

May 23,  · Organic synthesis is the process where a desired organic compound is constructed or prepared from commercially available materials. The objective of organic synthesis is to design the simplest synthetic routes to a molecule. A useful synthesis of acetylsalicylic acid was developed inpatented inmarketed under the trade name of “aspirin” by the Bayer Company in Germany.

The name aspirin was invented by. aspirin to diminish inflammation is due to its inhibition of the synthesis of prostaglandins. Aspirin alters the oxygenase activity of prostaglandin synthetase by moving the acetyl group to a terminal amine group 4.

Aspirin became commercially available in and today it is estimated that over a trillion aspirin tablets have been consumed by those in need of its curative effects.

In this experiment aspirin was synthesized from salicylic acid and acetic anhydride. aspirin to diminish inflammation is due to its inhibition of the synthesis of prostaglandins. Aspirin alters the oxygenase activity of prostaglandin synthetase by moving the acetyl group to a terminal amine group 4.

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Synthesis of aspirin lab
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