Preview

Erlenmeyer Synthesis

Good Essays
Open Document
Open Document
998 Words
Grammar
Grammar
Plagiarism
Plagiarism
Writing
Writing
Score
Score
Erlenmeyer Synthesis
In the second separation of this experiment, the Erlenmeyer flask with the first filtrate was put into a beaker so the filtrate was in the beaker. The beaker was then heated on a hotplate until near boiling. After the whey protein had precipitated, a vacuum filter was used to filter out the whey. These proteins were then air-dried. A qualitative test was done to indicate that the sample extracted was the protein whey. Again, a small test tube was used and 2 mL of protein test solution was put in the tube. Five drops of 10% NaOH and 2 drops of 0.5% CuSO4 were added to this tube. If a purple color showed, it would indicate there was protein in the test tube.
In the third separation of this experiment, the hood in the lab was used. The curds were placed in a 100 mL beaker and extracted using 30 mL of ethyl acetate. The curds were crushed with a stirring rod. This extraction was then gravity filtered through a funnel fitted with the filter paper. A rubber policeman was used to scrape the beaker to get as much casein as possible. This casein was then put aside in the hood safely. Boiling chips were put into an Erlenmeyer flask along with the filtrate collected. This flask was then put inside of the large beaker that was put to heat in the first separation of this experiment
…show more content…
The Fehling’s test was done to show the presence of carbohydrates. Two small test tubes were used and 5 mL of Fehling’s reagent was added to it. Five drops of 1% glucose was added to one test tube, the control. This tube was then boiled and if a brown-red precipitate was formed, it would indicate that there was a carbohydrate present. The other tube had 5 mL of the Fehling’s reagent put in it and five drops of the filtrate after the ethyl acetate was gone and the filtrate had been cooled. If this created a brown-red precipitate, it would indicate that there was a carbohydrate

You May Also Find These Documents Helpful

  • Good Essays

    chemsitry assignment

    • 1068 Words
    • 5 Pages

    The experiment was done in three parts: firstly the separation of sucrose, then the separation of Aspirin and the isolation of the unknown component.…

    • 1068 Words
    • 5 Pages
    Good Essays
  • Good Essays

    5.05 Ink Chromatography

    • 748 Words
    • 3 Pages

    The purpose of this laboratory investigation is to observe how chromatography can be used to separate mixtures of a solution.…

    • 748 Words
    • 3 Pages
    Good Essays
  • Satisfactory Essays

    Unknown Lab Results

    • 714 Words
    • 3 Pages

    The first sets of tests for our unknown consisted of whether or not fermentation had occurred in the Phenol Red Broth. The first part of this test was for glucose fermentation with my results being +, which represented acid fermentation based on the yellow broth, and G, which represented gas end-products in the tube. The second part of the test was for lactose fermentation with my results coming back -, indicating that no fermentation occurred as a result of the red broth. The final part of the Phenol Red Broth tested for sucrose fermentation and my results were were + based on the yellow broth, which meant fermentation with acid had occurred.…

    • 714 Words
    • 3 Pages
    Satisfactory Essays
  • Good Essays

    Bean Beetle Experiment

    • 881 Words
    • 4 Pages

    Next, transferred 200 uL of the crude extract to a set of microcentrifuge tube; the blank is created by adding 200 uL of the homogenizing buffer. Then 800 uL of pre-filtered dye reagent was added to each tube and vortexed for additional 10 seconds, followed by an incubation period of 10 minutes (Course Supplement for Bio 101, p. 71). We transferred 500 uL of the solution to the cuvette and measured the absorbance to 595nm. Using the BSA stock solution (2mg/mL=2000 ug/mL), we prepared the concentration of the protein standard by carrying out serial dilution at 2x, 5x, 10x, 20x and 40x. The 2x dilution was made by mixing 250 uL of BSA and 250 of the homogenizing buffer. The solution was then vortexed for 10 seconds. A similar procedure with different concentration of BSA and stock solution was carried out to find the other diluted concentrations. After the dilutions were made, 200 uL of the BSA concentration from the diluted tubes (2x, 5x etc.) were transferred to another microcentrifuge tube and 800 uL of filtered Bradford dye reagent was added to each microcentrifuge containing the BSA standard (Course Supplement for Bio 101, p. 72). The blank solution was created by adding 200 uL of homogenizing of the buffer. Then we incubated the tubes for 10 minutes and inverted 5 times before transferring 500 uL of the solution from each tube to the corresponding spectrometer cuvette; the absorbance was measured at 595 nm. The proper procedures were followed to discard the…

    • 881 Words
    • 4 Pages
    Good Essays
  • Powerful Essays

    Protein: Summary

    • 802 Words
    • 4 Pages

    ABSTRACT: In this lab, we are using a BioRad protein assay dye to determine the concentration of protein in our chicken. The dye binds to the amino acid residues, which allow us to find the concentration of protein (BioRad Protein Assay for Tissues). Our hypothesis was the longer chicken is cooked the less protein is available. To test our hypothesis, we made samples using our chicken and distilled water to determine how much protein was in the chicken. We found that our data supported our hypothesis; it showed that the longer our chicken was cooked the less protein that was in the chicken. As the chicken is cooked longer, the protein is denatured by the heat.…

    • 802 Words
    • 4 Pages
    Powerful Essays
  • Good Essays

    The purpose of this investigation was to see how the concentration of an enzyme affected the rate at which a substance was broken down. We did this by using a white protein called casein. Casein is found in milk powder, it is a protein and used mainly as a binding agent in foods, because it is mad to proteins and joins to a phosphoric acid it belong to a group called the phophoproteins. In terms of in milk it is said to be healthier if it is eaten when it is not denatured. It would become denatured if the protein loses its structure due to temperature, acidity or concentration. The enzyme used in this investigation was Trypsin, this is an enzyme used to degrade proteins, and it is a proteinase enzyme. Trypsin is one of the three main digestive proteinase, the two others include pepsin and chymotrypsin, the jobs for their types of enzymes is to break down dietary proteins e.g. casein, into peptides and amino acids. Trypsin is produced by the pancreas and has a very similar structure to chymotrypsin; the Trypsin we used was from a beefs pancreas.…

    • 857 Words
    • 4 Pages
    Good Essays
  • Better Essays

    The aim of the experiment which was carried out was to identify the unknown carbohydrates by subjecting them to a series of biochemical tests. The tests were as follows: Iodine, Solubility, Benedict’s, Acid Hydrolysis, Diastix and Barfoed test.…

    • 1059 Words
    • 5 Pages
    Better Essays
  • Good Essays

    This experiment deals with separating substances. The objective was to become familiar with the methods of separating substances from one another using decantation, extraction, sublimation techniques.…

    • 1037 Words
    • 5 Pages
    Good Essays
  • Good Essays

    Exp 4

    • 1145 Words
    • 5 Pages

    Protein purification is a series of processes intended to isolate a single type of protein from a complex mixture. Protein purification is vital for the characterization of the function, structure and interactions of the protein of interest. The various steps in the purification process may free the protein from a matrix that confines it, separate the protein and non-protein parts of the mixture, and finally separate the desired protein from all other proteins. Separation of one protein from all others is typically the most laborious aspect of protein purification. The most abundant protein found in milk is caseins and it can be removed by heat and low pH. The most general method to monitor the purification process is by running a SDS-polyacrylamide gel electrophoresis of the different steps. This method only gives a rough measure of the amounts of different proteins in the mixture, and it is not able to distinguish between proteins with similar apparent molecular weight. the purest, isolated form of bovine alpha-lactalbumin commercially available. Alpha-lactalbumin is the primary protein in human milk, and is therefore extremely important for infant nutrition. The structure of alpha-lactalbumin is well known and is composed of 123 amino acids and 4 disulfide bridges. The molecular weight of alpha-lactalbumin is 14.2K Daltons. Alpha…

    • 1145 Words
    • 5 Pages
    Good Essays
  • Good Essays

    2-3ml of extract, add two drops of alpha naphthol solution in alcohol shake and add conc. H2SO4 from sides of test tube.…

    • 1258 Words
    • 6 Pages
    Good Essays
  • Powerful Essays

    The objective of this experiment is to become familiar with the methods of separating substances from one another using decantation, extraction, and sublimation techniques.…

    • 1230 Words
    • 4 Pages
    Powerful Essays
  • Powerful Essays

    Experiment 2D

    • 1120 Words
    • 6 Pages

    The solvent (water) always travelled farther than the solute, except in the case of blue, which travelled the same amount as the solute. The blue had an Rf value of 1.0. The green and the unknown mixture both separated into their component colours and each component colour travelled a different distance.…

    • 1120 Words
    • 6 Pages
    Powerful Essays
  • Good Essays

    A mixture is a combination of two or more substances that are not chemically united and do not exist in fixed proportions to each other. Most natural substances are mixtures.…

    • 648 Words
    • 3 Pages
    Good Essays
  • Better Essays

    Protein Purification

    • 1222 Words
    • 5 Pages

    Egg white is acquired because it is where albumin is present. It is gently stirred to prevent denaturation and to mix the enzymes present in it. Later on, it is added with 1.0 M HOAc to remove calcium anions present. Then, it is sent to the centrifuge. The precipitate collected is discarded because it contains contaminants which aren’t needed for the experiment. Also, according to Campbell, if the…

    • 1222 Words
    • 5 Pages
    Better Essays
  • Good Essays

    Biology Lab

    • 807 Words
    • 4 Pages

    1. Solutions of different concentration were made from the stock solution and placed in test tubes.…

    • 807 Words
    • 4 Pages
    Good Essays