Methyl Red Voges-Proskauer Test Questions A.What is meant by the term biochemical profile? Biochemical profile is a variety of biochemical tests. These various tests are used to measure the constituents of plasma and serum in blood. B.What metabolic end product does the MR test for? The metabolic end product MR tests for are the different bacteria’s related to their individual patterns of glucose metabolism. C.What does an orange color indicate as a result for an MR test? An orange color as a result
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Methyl Red and Voges-Proskauer Test The Methyl Red test shows which bacteria are creating stable acids through mixed acid fermentation of glucose. This helps to identify enteric bacteria by examining how they metabolise glucose. Every enteric bacteria first produces pyruvic acid from metabolism of glucose. A methyl red positive enteric bacteria‚ uses the mixed acid pathway when breaking down pyruvic acid to different acids‚ like lactic‚ acetic‚ and formic acids. The Voges-Proskauer test determines
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Performed: September 9 ‚2011 SPECTROPHOTOMETRIC DETERMINATION OF THE ACID DISSOCIATION CONSTANT OF METHYL RED M.C. Caligagan ‚M.N.Q. Tolentino and M.Q. Clores Institute of Chemistry‚ College of Science University of the Philippines‚ Diliman‚ Quezon City‚ Philippines Received :September 21‚2011 ABSTRACT This experiment aims to determine the acid dissociation constant value of Methyl Red by means of spectrophotometry. Ten samples were spectrophotometrically analyzed under a UV-Vis spectrophotometer
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In this experiment‚ we used methyl benzoate from the last experiment with HNO3 and H2SO4 to synthesize methyl 3-nitrobenzoate. First we added methyl benzoate to 12 mL cooled conc. Sulfuric acid in a flask. In a separate flask‚ we made a solution of 4 mL conc. Sulfuric acid and 4 mL nitric acid and then added dropwise to the solution of methyl benzoate in an ice bath on a stir plate while maintaining the temperature of reaction between 5-15 °C. After the addition was complete we took the flask out
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para-hydroxybenzoic acid‚ which is why they are collectively called parabens. However‚ in contrast to its cousins‚ ethylparaben‚ butylparaben‚ and propylparaben‚ methylparaben receives its specific name owing to the fact that its chemical structure contains the methyl alkyl group. Methylparaben is found in several fruits‚ in particular blueberries‚ where it acts as an antimicrobial agent. Methylparaben is an anti-fungal agent often used in a variety of cosmetics and personal-care products. Methylparaben is commonly
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In this experiment the initial mass of the sodium carbonate used was 2.69g. In each titration‚ 3 drops of methyl orange was added to the sodium carbonate solution. With this information the titration can begin‚ and the results obtained are shown below: Titration readings Titration Rough 1 2 3 4 5 Initial 0.00 4.30 22.00 21.00 15.00 25.90 Final 4.30 22.00 38.60 37.60 32.60 42.20 Titre (cm3) 4.30 17.70 16.60 16.60 17.60 16.30 Therefore‚ the average titre would be calculated as follows;
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Objective To synthesis methyl orange by coupling diazotised sulphanilic acid with N‚N-dimethylaniline. Materials (Chemicals) Sulfanilic acid‚ 2.5% aqueous sodium carbonate solution‚ sodium nitrite‚ concentrated hydrochloric acid‚ N‚N-dimethylaniline‚ glacial acetic acid‚ 10% aqueous sodium hydroxide‚ saturated sodium chloride solution Apparatus 50 mL Erlemeyer flask‚ 250 mL beaker‚ test tube‚ hot plate‚ Buchner funnels Procedure In a 50 mL Elermenyer flask 1.2 g of sulfanilic acid and
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of cold water (remember to rinse the reaction flask with 10 mL of cold water and add it to the separatory funnel). Separate the lower aqueous layer. 5. Extract the organic layer (upper layer) with 100 mL of 5% sodium bicarbonate solution twice (test to be certain that the aqueous layer is basic to litmus‚ otherwise wash again). CAUTION: formation of carbon dioxide which will exert pressure inside the separatory funnel. 6. Extract the organic layer with 50 mL of water. Finally‚ add 15 mL of
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Sarah Muhs ID: 11325862 Nitration of Methyl Benzoate Post Lab: 1. Is the ester group of your starting material electron donating or withdrawing? Support your conclusion with resonance drawings. The ester group‚ CO2CH3‚ of the starting material was electron withdrawing. 2. Draw the mechanism of the nitronium ion reaction with the methylbenzoate. 3. Why does water stop the reaction? Water stops the reaction because of Le Châtlier’s principle. Since water is a product‚ when more is added it drives
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Nitration of Methyl Benzoate Introduction: Nitration is an example of an electrophile aromatic substitution reaction‚ where nitro (NO2) group is being substituted for a hydrogen on an aromatic compound. This is achieved by the formation of the nitronium ion by protonation of nitric acid from sulfuric acid. The zirconium ion is a strong electrophile and can react with aromatic compound such as Methyl benzoate to form an arenium ion intermediate. The arenium ion is then depronated to reform
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