O-Vanillin Lab Report

The contents of the reaction flask were slowly poured into the 250 ml Erlenmeyer flask which already contained 13.75 g ice and 25 ml of 10% H2SO2. The round bottom-flask was rinsed with 2.0 mL of 10% H2SO4 and 2.0 mL of diethyl ether, and the rinses were added to the mixture in an Erlenmeyer flask. Then, the mixture was swirled until all the salt was hydrolyzed, and the product distributed well into the ether layer. A

Next, about 10 mL of both solutions, Red 40 and Blue 1, were added to a small beaker. The concentration of the stock solution were recorded, 52.1 ppm for Red 40 and 16.6 ppm for Blue 1. Then, using the volumetric pipette, 5 mL of each solution was transferred into a 10 mL volumetric flask, labelled either R1 or B1. Deionized water was added into the flask using a pipette until the solution level reached a line which indicated 10 mL. A cap for the flask was inserted and the flask was invented a few times to completely mix the solution. Then, the volumetric pipette was rinsed with fresh deionized water and

In cycle one, the double displacement reaction, Cu(s) + 4HNO3(aq) → Cu(NO3)2(aq) + 2NO2(g) + 2H2O(l) occurred, the result of the reaction was that the reaction mixture began to bubble with the copper filling dissolving and a vapor like substance leaving the reaction. Furthermore, when water was added, the color change, from brown to a blue color pigment. Then in Cycle two, another double displacement reaction occurred, Cu(NO3)2(aq) + 2NaOH(aq) → Cu(OH)2(s) + 2NaNO3(aq), which resulted in the reaction becoming cloudy and a darker shade of blue. Following cycle two, a decomposition reaction occurred as the result of heat being administered to the mixture, thus the following reaction occurred in cycle three, Cu(OH)2(s) → CuO(s) + H2O(l). As a

Then the flask was filled the rest of the way with distilled water to the mark. Similar steps were taken for the rock solution. The rock solution from the prior lab was filtered into a volumetric flask (100mL), then 15 M NH4¬OH (8mL) was added to the flask. After that, the flask was filled to the mark with distilled water. Both flasks were then swirled to combine the solution

The purpose of this lab is to determine the specific isomer of the bromovanillin produced. In this experiment, vanillin is brominated to produce a mixture of isomers or one single isomer of bromovanillin. The possible product(s) formed are 2-bromovanillin, 5-bromovanillin, and 6-bromovanillin, as seen in Figure 1.1 By utilizing the bromination process of vanillin, one bromovanillin isomer can be formed as a result. As the starting material, vanillin can work with various electrophilic aromatic substitution reactions, due to the presence of aromatic double bonds within the structure.

After obtaining an homogeneous mixture, the flask was placed in an ice bath during five minutes next to a graduated cylinder containing 5.0 mL of concentrated sulfuric acid. The temperature of the ice bath was recorded to be 1.1 °C. Likewise, a second graduated cylinder containing 1.8 mL of nitric acid and 2.5 mL of sulfuric acid was immersed in the cold ice bath to keep the three different solutions at the same temperature. Thereafter, the cold 5.0 mL of H2SO4 were added to the erlenmeyer flask containing the acetanilide solution, which remained in the cold water for approximately another 4 minutes.

The percent yield calculated in this experiment was 49% that indicates errors occurred during this lab. Possible sources of error could have arisen in the decantation and recrystallization of the crystals. This process in the lab was difficult and was not

The final product is a blue liquid. There are many principles that are demonstrated by this experiment.

3. Upon adding 20 drops of NaOH, a white precipitate was formed signifying acidic impurity. In the second NaOH mixture, about 20 drops were administered and no precipitate formed indicating that the ample is more pure than before. Data: Weight of flask = 75.10 grams Weight of the flask with solids =

Abstract: The purpose of this experiment was to identify given Unknown White Compound by conducting various test and learning how to use lab techniques. Tests that are used during this experiment were a flame test, ion test, pH test, and conductivity test. The results drawn from these tests confirmed the identity of the Unknown White Compound to be sodium acetate (NaC2H3O2) because there were no presence of ions and sodium has a strong persistent orange color. The compound then will be synthesized with the compounds Na2CO3 and HC2H3O2 to find percent yield.

Conclusion: Based on the results of molarity from Trials 1, 2, and 3, it is concluded that our experimental for each trial is .410M NaOH, .410M NaOH, and .450M NaOH. The actual molarity of the NaOH concentration used was found to be 1.5M NaOH. The percent error of the results resulted in 72%. The large error may have occurred due to over titration of the NaOH, as the color of the solution in the flask was a darker pink in comparison for the needed faint pink. Discussion of Theory:

Thus, it was important to conduct the experiment on the same volume of bell pepper solution so only 30.0 cm3 from it was used, each time the experiment was carried

N-arylsulfonyl tryptophanderivatives were investigated as ligands for the reaction due to “the high π-electron-donating characterof the indole ring” (?) B-n-butyloxazaborolidine was used at 5 mol% to accelerate and control the reaction of cyclopentadiene and 2-bromoacrolein (-78 °C) in DCM. Enantioselectivity of the desired 2R adduct occurred at ca. 200:1 with a high yield. This catalyst can be used to enantioselectively produce gibberellic acid, a plant hormone, as well as the antiulcer agent, cassiol and eunicenone.

In test tube E, a colourless colour formed. It is because redox reaction occurred during the test. Idoine reduced into idoine ion ， which changre from brown to colourless. In test tube F, the iodine solution change from brown to purple . It is because the salt has a function of cofactor which will shorten the time for amylase to take to break down the

Properties of Roller Compacted Concrete with Pozzolan as Cement Replacement Material Introduction: Roller compacted concrete (RCC) gets its name from the heavy vibratory steel drum and rubber-tired rollers used to compact it into its final form. RCC has similar strength properties and consists of the same basic ingredients as conventional concrete_ well graded aggregates, cementitious materials, and water_ but different mixture proportions. The largest difference between RCC mixtures and conventional concrete mixtures is that RCC has a higher percentage of fine aggregates, which allows for tight packing and consolidation [1]. RCC may be considered for applications where no-slump concrete can be transported, placed, and compacted