CHEM 206- ORGANIC CHEMISTRY EXP 10-UNIMOLECULAR ELIMINATION REACTIONS Cansın Etli Lab Instructor: Emel Yılgör Experiment date:06.12.2010 Report Date: 20.12.2010 ABSTRACT In this experiment‚ the purpose was to investigate E1 elimination mechanism with the reaction of cyclohexanol to cyclohexene. The reaction was acid catalyzed dehydration of alcohol and with catalyst sulfuric acid cyclohexene was obtained from cyclohexanol. And the product
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CHEMICAL KINETICS: IODINE-CLOCK REACTION DATE SUBMITTED: 14 DECEMBER 2012 DATE PERFORMED: 7 DECEMBER 2012 ABSTRACT Chemical kinetics involving reaction rates and mechanisms is an essential part of our daily life in the modern world. It helps us understand whether particular reactions are favorable and how to save time or prolong time during each reaction. Experiment demonstrated the how concentration‚ temperature and presence of a catalyst can change the rate of a reaction. 5 runs of dilution
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Module 3: Kinetics of Chemical Reactions Introduction to Kinetics Chemical thermodynamics has answered the question “can a specified chemical reaction take place?” (i.e. is the reaction thermodynamically favourable?). • However‚ chemical thermodynamics hasn‟t answered the question “HOW FAST will a specified chemical reaction occur?” o Many thermodynamically favourable reactions are so slow (ex: metamorphic transformation of rocks‚ corrosion of marble sculptures owing to weathering) that they can
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Title : C2 Investigating the capacitance of a capacitor I. Objective : * To investigate the factor which affect the capacitance of a parallel-plate capacitor using a reed switch. II. Apparatus * Reed Switch * Signal generator * Capacitor Plates (1 pair) * Polythene spacers * Low voltage power supply * Voltmeter * Variable resistance * Light-beam galvanometer * CRO * Standard mass (eg. 100g ) * Connecting leads * Drawing board *
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Chemical Reactions & Equations CHEMICAL REACTION : In a reaction when the original state of the particle changes and it cannot be reversed by simple physical means‚ this type of reaction is known as chemical reaction. Example :- Fermentation of grapes‚ burning of wood etc. In this reaction we have seen that after burning of wood‚ coal is formed and we cannot make wood from coal. PHYSICAL REACTION : In a reaction when original state of the particle can be recovered by any means then this type of
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Kassidy Caviness- Thames Lab Partner: Dena Jackson Reaction lab “I certify that this lab report is my own work‚ except for properly referenced and cited information. I have adhered to all guidelines published in the student handbook on Academic Integrity‚ as well as all guidelines published for this class in the Syllabus and Academic Integrity Handouts.” Purpose- The purpose of this lab was to display to us a variety of different reactions using an eclectic of things in the chemistry lab: including
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AP Chem Exam - ‘98 1. Solve the following problem related to the solubility equilibria of some metal hydroxides in aqueous solution. (a) The solubility of Cu(OH)2(s) is 1.72 x10–6 g/100. mL of solution at 25° C. (i) Write the balanced chemical equation for the dissociation of Cu(OH)2(s) in aqueous solution. Cu(OH)2 Cu 2+ + 2 OH – (ii) Calculate the solubility (in mol/L) of Cu(OH)2 at 25 °C. (1.72 x10–6 g/0.100 L)(1 mol/97.5 g) = 1.76 x10–7 mol/L (iii) Calculate
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rate of reaction of the enzyme catalase. Background Information: Enzymes such as catalase are globular protein molecules with catalytic properties. A catalyst is a substrate which can alter the rate of reaction without itself undergoing any permanent change. As they are not changed my reactions which they catalyse‚ enzymes can be used over and over again. They are therefore quite effective in small amounts. All enzymes are specific as each one performs a particular reaction. Catalase
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CONCENTRATION ON REACTION RATE The aim of this experiment is to find the effect of varying the concentration of iodide ions on the rate of reaction between hydrogen peroxide and an acidified solution of potassium iodide: H2O2(aq) + 2H+(aq) + 2I⁻ → 2H2O(l) + I2(aq) The course of this reaction can be followed by carrying it out in the presence of small quantities of starch and sodium thiosulfate solutions. As the iodine molecules are produced they immediately react with the thiosulfate ions and are converted
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relations could be determined. Experimental results‚ which indicated an electronic influence on the regioselectivity‚ could be confirmed and appear to be predictable. The reaction follows a [3þ2] mechanism. We additionally report results on the experimentally observed competing dihydroxylation reaction and the ligand-induced reaction rate acceleration. Introduction Sharpless et al. reported in the 1970s an aza-analogon of the osmium-catalyzed cis-vicinal dihydroxylation (DH)1 of alkenes‚ the
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