Describe an alternative method for evaporation of the CH2Cl2 Can be steamed and then rinsed with ethyl acetate for several hours‚ and then rinsed with water‚ or can be soaked in a bath of CO2 and run through water‚ making carboxylic acid. (2) Caffeine: (4) Repeated exposure can produce general deterioration of health by an accumulation in one or many human organs. First Aid Measures: Eye contact - Immediately flush eyes with plenty of water for at least 15 minutes. Cold water may be used. WARM
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INDEX SL.NO. | CONTENTS | PAGE NO: | 1. | INTRODUCTION | 1-2 | 2. | LEAD | 3 | 3. | PREPARATIONS OF LEAD | 4-6 | 4. | LEAD POISONING | 7 | 5. | SOURCES OF LEAD | 8-9 | 6. | WHY LEAD IS HARMFUL? | 10 | 7. | ABSORPTION‚DISTRIBUTION AND ELIMINATION | 11 | 8. | RISK FACTORS | 12 | 9 | SIGNS AND SYMPTOMS | 13-17 | 10. | FATAL DOSE AND FATAL PERIOD | 18 | 11. | COMPLICATIONS | 19 | 12. | TESTS AND DIAGONOSIS | 20 | 13. | TREATMENT AND DRUGS | 21-22 | 14. | POST MORTEM APPEARANCE
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which was done using the process of fractional distillation. Five milliliters of dicyclopentadiene was utilized in the distillation at the temperature of 40˚C for approximately 20 minutes. Next 0.20g of maleic anhydride was dissolve in 2mL of ethyl acetate. Then it was
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The purpose of Module 11A was to test for the presence or absence of a particular set of functional groups through the use of wet chemical tests. In this manner‚ Unknown A which was a colorless solution‚ was first tested with 2‚4-DNP which after mixing for a few seconds formed a bright yellow precipitate. Although this confirms the presence of either a ketone or aldehyde group‚ one simple chemical test does not completely specify the presence or absence of other functional groups. Therefore‚ a second
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EFFECTS OF VOLATILE ORGANIC COMPOUNDS (10244818) Volatile organic compounds (VOCs) are organic chemical compounds that have high enough vapor pressures under normal conditions to significantly vaporize and enter the atmosphere. According to EPA ’s Terms of the Environment‚ a volatile organic compound is "any organic compound that participates in atmospheric photochemical reactions except those designated by EPA as having negligible photochemical reactivity." VOC can also stand for the term “volatile
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Microbial Cell Factories BioMed Central Open Access Research Metabolic engineering of Saccharomyces cerevisiae for the production of n-butanol Eric J Steen1‚2‚ Rossana Chan1‚3‚ Nilu Prasad1‚3‚ Samuel Myers1‚3‚ Christopher J Petzold1‚3‚ Alyssa Redding1‚3‚ Mario Ouellet1‚3 and Jay D Keasling*1‚2‚3‚4 Address: 1Joint BioEnergy Institute‚ 5885 Hollis Avenue‚ Emeryville‚ CA 94608‚ USA‚ 2Department of Bioengineering‚ University of California‚ Berkeley‚ CA 94720‚ USA‚ 3Physical Biosciences
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Column and thin layer chromatography of plant pigments CHEMISTRY 201L EXPT 04 PAGE 01 - 12 Noel Angelo P. Kalacas*‚ Hanna Mae Laluces‚ Ina Bianca Lanuza Department of Chemistry‚ College of Science *Corresponding author; e-mail: knight_BeNcH66@yahoo.com Abstract Chromatography is a powerful technique for separating and/or identifying the components in a mixture. There are different types of chromatography and each has its own strengths and weaknesses. In this experiment‚ pigments of the
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vinegar compared to the standard solution which Trading Standard provides. What is a Vinegar? Vinegar is a versatile liquid that is created from fermentation of ethanol‚ this is done by when yeast or any type of bacteria. These converts sugar in ethyl alcohol and carbon dioxide. Fermentation begins after the glucose enters the cell. The glucose is broken down into pyruvic acid and is converted into CO₂‚ ethanol and energy for the cell. It also contains acetic acid‚ this acid is the key ingredient
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Abstract: The objective of this experiment was to successfully prepare an endo‚cis-diacid from the synthesis of the bicyclic anhydride (cis-Norbonene-5‚6-endo-dicarboxylic anhydride). The percent yield of the product was calculated and found to be 39.01%. The infrared spectroscopy confirmed the presence of a O-H group with a stretch at 2948.03 1/cm and the presence of C=O with a stretch at 1698.93 1/cm. Melting point determination found the melting point range of the products to be 149.2-164.1 for
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Nitration and Purification of Bromobenzene Abstract: An electrophilic aromatic substitution reaction was performed on bromobenzene with nitric acid producing both 2-bromonitrobenzene and 4-bromonitrobenzene. Products of the reaction were purified through multiple recrystallizations and column chromatography creating multiple crops of a yellow powder. The percent yield of products was determined to be 51%. The melting point of Crop 1 was found to be 110-115 °C‚ and Crop 2 was found to be 37-90
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