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    Preparation of PoPD fabricated of Mg-Al layered double hydroxides 0.356 g of Magnesium nitrate (0.3 M) and 0.169 g of Aluminium nitrate (0.1 M) solution were containing in 100 ml beaker with continuous stirring (1:3 ratio) and followed by 0.700 g of urea (0.5 M) was added into the solution. The reaction mixture was maintained basic medium using 1 g of NaOH solution was added drop by drop into the above metal solution. The mixture was stirred for 30 min and the precipitate was poured into the 50

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    The Basics of Nmr

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    The Basics of NMR Chapter 1 INTRODUCTION [pic] NMR Spectroscopy Units Review [pic] NMR Nuclear magnetic resonance‚ or NMR as it is abbreviated by scientists‚ is a phenomenon which occurs when the nuclei of certain atoms are immersed in a static magnetic field and exposed to a second oscillating magnetic field. Some nuclei experience this phenomenon‚ and others do not‚ dependent upon whether they possess a property called spin. You will learn about spin

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    2a: Infrared Spectroscopy and Analgesic Drug Identification Abstract: To be able to understand how organic soluble compounds could be isolated from non-organic components‚ a chromatographic separation process was used. The objective of the analgesic drug identification is to isolate the organic compounds/ active ingredients in an unknown drug. The identity of the drug was determined through melting point‚ percent recover‚ and Rf values. The comparable data for acetaminophen from the manufacturer

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    Among them were dehydration‚ isolation‚ drying‚ and distillation. We used all of these techniques to get the product we were looking for. In addition to these experimental techniques we also verified our product via spectroscopy which is a new technique. Using IR spectroscopy we were able to specifically analyze the functional groups on our product. Results and Discussions: Reaction Equation: Theoretical Yields: Based on limiting moles of product -Based on C7H14O 24 mL C7H14O

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    cloves using steam distillation‚ perform infrared spectroscopy on the sample‚ and analyze the IR to identify the major constituent in the clove oil. The first day the clove oil was removed from the ground cloves into an aqueous solution then removed from the water using DCM. The sample was left in a sealed container for one week and then isolated by drying the sample and removing the DCM. After the clove oil was isolated it was analyzed using IR spectroscopy. Experimental Isolation of Clove Oil: The

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    1-Bromobutane Lab Report

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    simple organic chemistry experiment is described that investigates the kinetics of the reaction between 1-bromobutane (BuBr) and iodide (I−) as followed by observing the disappearance of BuBr and the appearance of 1-iodobutane (BuI) using 1H NMR spectroscopy. In small groups of three to four‚ students acquire data to examine the concentrationdependence of both the organic substrate and the nucleophile under pseudofirst-order and second-order conditions. After

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    Identification of Unknown Organic Compound by Melting Point (M.P)‚ Boiling Point (B.P) and Infrared Spectroscopy Methods and Background The main objective of this lab is to identify the given unknown organic compounds with various methods. Identification of an unknown compound is important to perform through the process of melting point (M.P)‚ boiling point (B.P) and Infrared spectroscopy (I.R). Index of Hydrogen deficiency (IHD) and elemental analysis makes an experiment more efficient in

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    concentrated sulfuric acid as a catalyst. The product was washed with sodium hydrogen carbonate‚ as well as with water‚ then dried with anhydrous sodium sulfate. The product was then distilled using a Hickman still and characterized using infrared spectroscopy. The percent yield of isopentyl acetate was 61.52%. This may have been low due to not all of the condensed product being removed from the Hickman still‚ some product being lost during transfer of the product from the reaction tube into the Hickman

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    Objective: To determine the concentration and equilibrium constant for a reaction of colored product using absorption spectroscopy‚ to create a calibration curve for determining equilibrium concentrations by applying Beer’s law and to force the completion of a reaction by applying Le Châtelier’s principle. Procedure: A diluted solution was made from the stock of 0.0025 M Fe(NO3)3 by diluting 4.0 mL to exactly 100.00 mL‚ using serological pipet and volumetric flask. The concentration of the diluted

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    Alkene From Cyclohexanol

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    Alkene Synthesis from Alcohol: Preparation of Cyclohexene From Cyclohexanol 5/29/14 Abstract: A 42.89% yield cyclohexene was successfully synthesized from 10.0 mL cyclohexanol by unimolecular elimination (E1) through the dehydration of cyclohexanol and confirmed via a bromine test and the IR spectra. Introduction: Alkenes are hydrocarbons that have carbon–carbon double bonds and are one of the many functional groups in organic molecules. Alkenes are sp2 hybridized

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