BENZOPINACOL FROM BENZOPHENONE BY PHOTOREDUCTION IN GREEN CHEMISTRY. 1 Lata.C.Potey‚ 2* Dr. Satish B. Kosalge‚ 3 Rajeshwari S. Sarode 1 2 Assistant Professor‚ Hi-Tech College of Pharmacy‚ Chandrapur. Principal‚ Hi-Tech College of Pharmacy‚ Chandrapur 3 Assistant Professor‚ Hi-Tech College of Pharmacy‚ Chandrapur. Date Received: 11 TH Jan 2014 Date of Accepted: th 16 Jan 2014 Date Published: 18th Jan 2014 Abstract: This is free radical reaction and reduction of
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Chromatography Photochemical Smog Lecturer’s Name : Ms. Usha Nanthini Table of Content No. | Content | page | 1. | Paper Chromatography | | | 1.1 Definition | | | 1.2 Background | | | 1.3 Rf Values | | | 1.4 Principles of Paper Chromatography | | | 1.5 Procedure of Paper Chromatography | | | 1.6 Uses of Paper Chromatography | | | 1.7 Application of Paper Chromatography | | 2. | Photochemical Smog | | | 2.1 Definition | | | 2.2 Causes of Photochemical Smog
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Photochemical Smog Gifted Chemistry IB Alternative Assessment 1997 March 19 Historically‚ the term smog referred to a mixture of smoke and fog‚ hence the name smog. The industrial revolution has been the central cause for the increase in pollutants in the atmosphere over the last three centuries. Before 1950‚ the majority of this pollution was created from the burning of coal for energy generation‚ space heating‚ cooking‚ and transportation. Under the right conditions‚ the smoke and sulfur dioxide
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. Yes‚ comparably to TLC plate 2 and 3. The benzophenone is more neutral but as the same time its nonpolar‚ being that Silica gel in TLC 2 was polar and the solvent ethyl acetate-hexane is non-polar it moved relatively with the solvent. The stationary phase in TLC 3‚ alumina is non polar and the solvent ethyl acetate is polar so from the ideal that polar does not attract non-polar benzophenone stick stronger to alumina non-polar rather than moving up with polar solvent ethyl acetate as it did in
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Indian Institute of Technology‚ Kanpur PHOTOCHEMICAL MACHINING (PCM) ME662 Advanced Machining Processes Tarun Mankad Y4456 October 05‚ 2007 CONTENTS INTRODUCTION 5 PROCESS OUTLINE 7 PROCESS COMPONENTS 8 PCM PRODUCTS 21 COST DRIVERS 27 ADVANTAGES OF PCM 28 CONCLUSION 29 REFERENCES 31 LIST OF ILLUSTRATIONS Illustration 1: the current PCM process 7 Illustration 2: process flow-chart 9 Illustration 3: etch profile development with time 14 Illustration
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wavelength Percentage concentration (methanol: water) Peak H value (height equivalent to a theoretical plate) (mm) 230nm 80:20 Phenol 0.0373 Benzophenone 0.0196 Naphthalene 0.0164 235nm 80:20 Phenol 0.0327 Benzophenone 0.0203 Naphthalene 0.0147 260nm 80:20 Phenol 0.0318 Benzophenone 0.0202 Naphthalene 0.0146 Figure 11: table for the height equivalent of the theoretical plates. It can be observed that the H values or height equivalent to a theoretical plate for phenol at the three wavelengths
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Triphenylmethanol from Benzophenone Purpose: The purpose of this experiment was to synthesize the tertiary alcohol triphenylmethanol from a Grignard reagent‚ phenyl magnesium bromide. The Grignard reagent was synthesized from bromobenzene and magnesium and then reacted with benzophenone to produce triphenylmethanol. It was important that water be excluded from the reaction‚ in order to prevent the formation of benzene. The reaction of phenyl magnesium bromide and benzophenone was quenched with sulfuric
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Experiment Date: 3/12/2012 Photochemistry: Photoreduction of benzophenone and rearrangement to benzpinacolone Abstract: In this experiment Benzpinacolone was synthesized in a process that contained two steps. First the photoreduction of benzophenone in 2-propanol‚ which was done by placing the flask under sunlightfor the absorption of the UV rays to carry out the reaction. Then the second part was the dehydration of benzpinacol to benzpinacolone‚ where the benzpinacol product was converted
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different melting point expected for the pure compound and a broadening of the melting point range. Such an observation would indicates that a compound is impure. In experiment 3.2‚ 0.120g sample of benzophenone was obtained from stock and crushed into a fine powder. Two samples of the benzophenone were loaded into a capillary tube. The capillary tubes were then individually placed in a Mel-Temp apparatus where they were gradually heated at a steady rate of 1º/minute. The melting rate was manually
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Photochemical Synthesis of Benzopinacol and its Acid-Catalyzed Rerrangement Product Benzopinacolone M.E.G. Balita Institute of Chemistry‚ University of Philippines‚ Diliman‚ Quezon City Date Performed: February 18‚ 2011 Date Submitted: March 4‚ 2011 Abstract In this experiment it is aimed to synthesize benzopinacol through photochemical reaction of benzophenone and‚ benzopinacolone via acid-catalyzed rearrangement of benzopinacol. In this experiment‚ mixture of benzophenone‚ isopropyl
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