results were obtained for acidity‚ 0Brix‚ Reducing sugars and ascorbic acid with regards to the treatments as well as storage. The pH was non significantly affected by treatments; however‚ storage had significant effect on it. The acidity‚ 0Brix and reducing sugars increased while pH and ascorbic acid decreased during storage. The acidity and pH changed gradually in all treatments while 0 Brix‚ reducing sugars and ascorbic acid changed differently and maximum variations were observed in the treatment
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Preparation of Bromotriphenylmethane Abstract The structure of a major component of star anise oil was derived by analyzing its IR spectroscopy melting point of after oxidation and purification. From the evidence obtained‚ it was concluded that the exact structured should be p-methoxybenzoic acid. Introduction The purpose of this experiment is to determine the structure of the major component of star anise oil. It is already known that this component has a molecular formula C10H12O. This
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Buffer Preparation (Gozani Lab) 1. 1 M Tris-HCl Buffers pH Volume (L) TrisBase (g) HCl (ml) pH 7.0 2 242.2 150-155 pH 7.5 2 242.2 120-125 pH 8.0 2 242.2 80-85 Autoclavable. 2. EDTA 0.5 M (pH8.0) 0.5M‚ 1L: 148 g EDTA + ~30-40 g NaOH to adjust pH (or 186 g EDTA-Na.2H2O + ~20 g NaOH) Note: pH adjusted by NaOH is essential for solubility. Autoclavable. 3. TAE DNA Electrophoresis Buffer (50 X) (2 M Tris‚ 50 mM EDTA) 2L 484 g Tris 114.2 ml glacial acetic acid 200 ml 0.5 M EDTA 8.0 To make
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Penicillium chrysogenum ATCC 16520 (Obtained from American Type Culture Collection) is used for the production of Penicillin. Preparation of Different Salts of Phenyl acetic acid. Sodium phenyl acetate For 100 ml preparation‚ few grams of PAA (of known percentage) are dissolved in certain volume of De-Mineralized water. The pH of the solution is maintained between 6.6-7 by adding NaOH in drops. Molecular Weight-159. Potassium phenyl acetate For 100 ml preparation‚ few grams of PAA (of known percentage)
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20 – 03 – 13 EXPERIMENT: - PREPARATION OF POLYURETHANES AIM Synthesis of polyurethanes OBJECTIVES - Mixing a diisocyanate and a diol in polyurethane synthesis of two distinct products. - Comparing polyurethane from castor oil to that made from polyethylene glycol. - To establish the type of foams in terms rigidity or flexibility. THEORY Polyurethanes‚ also known as polycarbamates‚ belong to a larger class of compounds called polymers. Polymers are macromolecules made up
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Introduction This lab’s purpose was to determine whether Salicylic Acid made from methyl salicylate is the same as Salicylic Acid made from benzene. This information can be found by comparing the difference in melting points of the two samples of Salicylic Acid. Here are the physical properties of Salicylic Acid and the mechanism of reactions that occurred in this lab. How Salicylic Acid is derived: Procedure/Results First‚ .26mL of 2.0mmol methyl Salicylate was measured and put
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An Unknown Amino Acid From Titration Abstract Experiment 11 used a titration curve to determine the identity of an unknown amino acid. The initial pH of the solution was 1.96‚ and the pKa’s found experimentally were 2.0‚ 4.0‚ and 9.85. The accepted pKa values were found to be 2.10‚ 4.07‚ and 9.47. The molecular weight was calculated to be 176.3 while the accepted value was found to be 183.5. The identity of the unknown amino acid was established to be glutamic acid‚ hydrochloride. Introduction
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L’Oreal : Strategies for the Indian Market Session 4: Preparation Questions 1. Evaluate L’Oreal’s entry strategy in the Indian market with respect to the product‚ promotion‚ pricing and place decisions? 2. What have been the changes in the marketing strategy of L’Oreal in the last 8 years? Evaluate them with respect to selection of product / market and each element of the marketing mix? 3. What factors helped the rapid adoption of Excellence colorants among its target customers?
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EXPERIMENT 4: Synthesis of Salicylic Acid from Wintergreen Oil Abstract: The purpose of this experiment is to take methyl salicylate (wintergreen oil) and by heating it under reflux with NaOH as a solvent‚ and then cooling the mixture with H2SO4 as another solvent‚ synthesize salicylic acid. The final step involves purify the product to produce as pure a sample of salicylic acid as possible. This process allowed for the successful production of 1.406g salicylic acid‚ an 82.70% yield. The NMR and IR
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Learning Activity 1 Preparation of Acetanilide Abstract Recrystallization is a common method of purifying organic substances through the difference in solubility at different temperature. In this experiment‚ acetanilide was produced by acetylation of aniline with acetic anhydride. The crude acetanilide was dissolved in a solvent in a heating water bath. The solution was cooled slowly in an ice bath as crystals form out. As the compound crystallizes from the solution‚ molecules of other compounds
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