The melting point of the experimentally synthesized Aspirin product was found to be between 126-129 ˚C. This temperature range of initial to final melting point has a small and sharp temperature range of only 3˚C, which is within the acceptable limits of the 128-137˚C1 literature value for Aspirin (Acetylsalicylic Acid/2-acetoxybenzoic acid), if located slightly toward the beginning of the literature melting temperature range. Therefore, the narrow melting point range, which falls within the standard literature value range results, indicate the reliability purity of the sample. Had the melting point been higher than the literature value, but maintained a sharp melting point range, the compound could have still indicated a pure sample. A lower …show more content…
The reason for this is due to the alcohol functional group present in the salicylic acid starting material, as it has a higher Rf value when TLC is run on the compound in which it is contained at the start of the reaction. TLC of the Aspirin product contained an ester functional group, which was expected to have a lower Rf due to residual hydrogen bonding which occurred between the hydroxyl group of the carboxylic acid and adjacent carbonyl of the ester. Experimental results followed this expected outcome, indicating the successful synthesis of the experimental aspirin product, which maintained a lower Rf value than the reaction starting material (Rf Data Figure 1). Experimental IR results indicated the presence if characteristic wavelength peak values that are found in a successfully synthesized Acetylsalicylic Acid (2-acetoxybenzoic acid) or Aspirin product. The IR spectra revealed the presence of the ester functional group via a peak at 1760cm-1 indicating C=O carbonyl bonding of an ester. Also indicative of the ester functional group are the wavelength peaks between 1250-1050cm-1, signaling the presence of -C-O- bonding. Additional peaks in the spectrum, such as the shaky broad peak
The other possibility for the unknown neutral, 1,4-dimehtoxybenzone, would have had an H NMR spectra with two peaks; however, the spectra obtained did not show chemical shifts for an aromatic ester group and had many hydrogens in the aromatic
As different bonds require different amounts of energy to bend and stretch, they absorb and transmit different amounts of radiation. This data is then collected by the spectrometer and transposed into graph form. The different amounts of absorbance for various functional groups and types of bonds have been established and can be used to identify compounds. Also, an IR spectrum can be compared to known “fingerprint” spectra in order to identify the compound. When compared to the fingerprint spectrum for 1-bromobutane found in Experimental Organic Chemistry, the IR spectrum collected from the data was very similar.
Therefore, liquid-liquid and acid-base extraction techniques were successfully performed to separate the components of the Excedrin tablet. According to the TLC analysis results, the compounds (aspirin, acetaminophen, and caffeine) were successfully isolated from the analgesic (Excedrin tablet). In figure 1, the separation of the compound in the TLC analysis correlates with the TLC analysis in figure 2. Furthermore, Rf index calculations of the TLC analysis demonstrated that the compounds (aspirin, acetaminophen, and caffeine) were separated. The Rf calculations of aspirin in table 1 shows an Rf value of .491; however, in table 2 the Rf value of aspirin was calculated to be .784.
The difference in this chemical and physical properties will aid in their separation. Processes like solubility, gravitational filtration and recrystallization will be used to separate the substances present in Panacetin. The melting and boiling point of the substances will help in concluding on which of these compounds will be presented at the end of experiment. Procedure and observation The Panacetin content was weighed approximately 3.0493g and transferred to the Erlenmeyer flask; 75ml of dichloromethane (CH¬2CL2) was added to the content. The dichloromethane (CH2Cl2) dissolved the sucrose, leaving the active unknown agent and aspirin behind.
The boiling point range of Unknown 30A was 65.0 °C-67.2 °C. The two degrees difference in the boiling point range indicated that there were very few impurities presented in the liquid. The theoretically possible identities of the unknown were primary amines that contained higher boiling points than the range because of the higher altitude lab. However, sec-butylamine, with a boiling point of 63 °C, was included as a possible identities because it was only two degrees off of the range. Therefore, it was too early on in the experiment to eliminate a potential identity that was very close to the range.
Pages 96-98 in Chemistry 110 Lab Manual. Wilfrid Laurier University, ON, Canada. Abstract: The purpose of this experiment was to determine the level of purity by using the values for melting point and absorbance and chemically synthesizing aspirin by using phosphoric acid as a catalyst.
Audience: This paper is written with the intent of addressing an audience consisting of advanced high school students and lower division college students, who are interested in learning what happens to their bodies internally when ibuprofen is consumed. Students should have taken a general chemistry, and biology course as a prerequisite. It is expected that the student have some previous knowledge on nomenclature, spectroscopy, and basic internal organs.
We were able to eliminate certain ingredients like chlorpheniramine because this ingredient was the only neutral and the properties were not similar to the unknowns. The other team identified that the unknowns included all the ingredients except for the acetylsalicylic acid. They came up with their conclusions based off during the starch test both unknowns contained starch. They had different results than our team during the acetone solubility test. Team 2 found that both unknowns were acetone soluble, but our team found only unknown B was acetone soluble.
Aspirin is considered a “polydrug” due to its variety of uses stretching from pain-relief to disease prevention. Salicylic acid is derived from the bark and leaves of the willow tree. Salicylic acid belongs to a group of phytochemicals which have been shown to have positive effects on human health. Salicylic acid is a phenolic compound that can be found in a variety of plants and is a crystal organic carboxylic acid. However, it is more commonly viewed as the primary metabolite and active compound of acetyl salicylic acid, which has been used as an anti-inflammatory drug by physicians for over 100 years.
The Problem: How does temperature affect the dissolving time of an antacid tablet? Antacid tablets are medicines that help neutralize the acid in your stomach. Antacid tablets are made of numerous numbers of components, such as sodium bicarbonate (baking powder), magnesium hydroxide, critic acid, and many others. When Antacid tablets are placed in water, they undergo a chemical reaction, where the sodium bicarbonate breaks apart to make sodium and bicarbonate ions. When the bicarbonate ions collide with hydrogen ions, it produces carbonic acid.
The objective of this experiment was to use an aldol condensation reaction to synthesize 3-nitrochalcone from 3- nitrobenzaldehyde. This was accomplished with a Diels-Alder reaction that utilized 3-nitrobenzaldehyde, acetophenone, ethanol, and sodium hydroxide. The mechanism for the synthesis of 3-nitrochalcone is presented in Figures 1 and 2. The alpha carbon on the acetophenone is deprotonated. This is followed by the attack of the alpha carbon anion on the carbonyl carbon on the 3-nitrobenzaldehyde.
The main objective of this experiment was the formation of phenacetin from the synthesis of acetaminophen. This was done through a chemical reaction known as the Williamson ether synthesis using techniques of refluxing, vacuum filtration and recrystallization incorporating a mixed solvent system. A further objective of this experiment was to study the formation of the product (phenacetin). Such validation was completed by using techniques for determining the melting point, calculating percent yield, and IR (infrared spectroscopy) of the resultant product.
TLC was used to identify the actual unknown product as well as other products/reactants present in the filtered solution. The procedure was conducted by placing a TLC plate in a developing chamber that is filled with a small amount of solvent. The solvent cannot be too polar because it will cause spotted compounds on the TLC plate to rise up too fast, while a very non-polar solvent will not allow the spots to move. The polarity of the spots also determines how far it moves on the plate; non-polar spots are higher than polar ones. After spots on the TLC form, the Rf values are calculated and used to analyze the similarity of the compounds.
To analyze the acetanilide product of the reaction, 1H NMR and IR were used. Results, Discussions, and Conclusions In this experiment, acetanilide was synthesized via nucleophilic acyl substitution from both acetic anhydride and aniline. During this reaction, aniline acts as the nucleophile and acyl (CH3CO-) group from acetic anhydride acts as the electrophile.
Decomposition of Aspirin Studied with UV/Visible Absorption Spectroscopy Aims: To determine the concentration of salicylic acid, formed from the hydrolysis of Aspirin, at regular intervals using the UV/Visible Absorption Spectroscopy From the concentration of salicylic acid, concentration of Aspirin to be determined using an equation Calculate the rate constant of this reaction and its order from a plot of graph of ln(aspirin) vs time Discuss the overall flaws and improvements to the experiment Results: As per schedule1, 0.212g of aspirin was added to 50 ml boiling water to form salicylic acid in a 100 ml flask, of which 1 ml was then pipetted to a 50 ml volumetric flask at the 5th min. Following an ice bath, the solution was mixed