Caroline Guidry Dr. Beverly A. Clement Organic Chemistry 2423‚ Section 304 25 October 2017 Lab 6: Natural Products I The main goal of this experiment was to employ isolation techniques to derive chemicals from two different natural sources and study their properties (Clement 91). The two natural sources used in this experiment were an orange (the peel contains limonene‚ which is a terpene) and a dichloromethane solution of clove oil (which contains eugenol‚ an acetogenin). To isolate the eugenol
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attraction between two molecules‚ pulling them together (also known as London dispersion forces). The magnitude pof Van der Waals force depends on the relative molecular mass‚ high mass produces a larger force. Boiling points of the alkanes data and alkenes data These very clearly illustrate the effect of increasing Van der Waals attractions as the relative molecular mass increases. The influence of branching in the alkanes can also illustrate the effect of different surface areas on the Van der Waala
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w w ap eP m e tr .X w om .c s er June 2003 INTERNATIONAL GCSE MARKING SCHEME MAXIMUM MARK: 40 SYLLABUS/COMPONENT: 0620/01 CHEMISTRY (Multiple Choice) Page 1 Mark Scheme IGCSE EXAMINATIONS – June 2003 Syllabus 0620 Question Number Key Question Number Key 1 2 3 4 5 C B A D A 21 22 23 24 25 B D A B D 6 7 8 9 10 C A A B C 26 27 28 29 30 B D D D B 11 12 13 14 15 B D C D
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Fundamentals Of Petroleum Engineering SKPP 1313 INTRODUCTION ARIFF OTHMAN Department of Petroleum Engineering Faculty of Petroleum & Renewable Engineering Universiti Teknologi Malaysia 1 COURSE CONTENT What is Petroleum Engineering? What Does Petroleum Mean? Generation of Petroleum Chemical Composition of Petroleum Petroleum Products Fractional Distillation The First Oil Well History of Oil in Malaysia Production Sharing Contract MOHD FAUZI HAMID
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(Author’s name) (Professor’s name) (Course details) (Date Abstract The aim of the lab was to separate and analyse analgesic drugs in a drug tablet. The method used to separate the components was Thin Layer Chromatography (TLC) with silica adsorbent as the stationary phase and 0.5% glacial acetic as the mobile phase. In one plate‚ five known samples were used as the reference‚ that is: Aspirin; Caffeine; Ibuprofen; and Salicylamide. Aspirin and Salicylamide were the only samples that fluoresced
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The report “China Coal Tar Industry Report‚ 2013-2016″ by Research in China is now available at chinamarketresearchreports.com. Contact sales@chinamarketresearchreports.com with “China Coal Tar Industry Report‚ 2013-2016” in subject line and your contact details to purchase this report or get your questions answered. Synopsis Amid China’s economic slowdown in 2013‚ the coke price continued to fall and the coking industry remained weak‚ thus the situation of oversupply would not get changed in
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Experiment 6: Synthesis of an Alkyl Halide Maria Alexandria Buraga Ammuyutan Institute of Chemistry‚ University of the Philippines‚ Diliman‚ Quezon City 1101 Philippines ------------------------------------------------- Department of Food and Science Nutrition‚ College of Home Economics‚ Univeristy of the Philippines‚ Diliman‚ Quezon City 1101 Philippines ------------------------------------------------- ABSTRACT ------------------------------------------------- Alcohols react with hydrogen
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dipole. 6 Structure and Properties of Alcohols •Alcohols have an H atom bonded to an O atom‚ making them capable of intermolecular hydrogen bonding. •All of these properties give alcohols much stronger intermolecular forces than alkanes and alkenes. 7 Structure and Properties of Alcohols •Therefore‚ alcohols have higher boiling and melting points than hydrocarbons of comparable size and shape. stronger intermolecular forces higher boiling and melting point 8 Structure and Properties
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Intensity s m m m s s s m w w m-w m-w m-w s s s s s s s Alkanes -CH3 -CH2Alkenes (stretch) (bend) (bend) (stretch) CHARACTERISTIC INFRARED FREQUENCIES (bend) Aromatic (stretch) (out-of-plane bend) Alkyne Aldehyde C=C C C C=O (stretch) Alkene (stretch) Aromatic (stretch) Alkyne (stretch) Aldehyde (stretch) Ketone (acyclic) Carboxylic Acid Ester Amide Anhydride Alcohols‚ ethers‚ esters carboxylic acids Alcohols‚ phenols Free H-bonded Carboxylic acids Primary and secondary amines Nitriles
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guess paper 1. Express the rate of following reaction in terms of disappearance of hydrogen in the reaction. 3H2(g) + N2(g) 2NH3(g) 2. What is peptisation? 3. Write Reimer Tiemann reaction. 4. Why is CO stronger ligand that Cl-. 5. Write structure of 2-(2-Bromophenyl)butane. 6. Complete the reaction C6H6+R COCl 7. Why pentahalides more covalent than trihalides? 8. What is difference between nucleoside and nucleotide? 9. Explain the following- (a) Gattermann Koch
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