68g)‚ anhydrous diethyl ether (15 cm3)‚ a crystal of iodine and a stirrer bar were added to the round bottomed flask (250 cm3) and anhydrous diethyl ether (25 cm3) and dry bromobenzene (15.7g) were added to the dropping funnel‚ ensuring tap was closed. Dropping funnel was opened slightly allowing a small amount of bromobenzene
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Grignard Synthesis of Triphenylmethanol Aim The aim of this experiment was to prepared Grignard reagent (phenylmagnesium bromide) from bromobenzene and magnesium‚ to use the reagent prepared to synthesise a tertiary alcohol (triphenylmethanol) by reacting reagent and ester (methyl benzoate)‚ and the product formed is analyse by infrared spectroscopy (IR)‚ melting point‚ thin layer chromatography (TLC)‚ gas chromatography mass spectrum (GCMS) and finally Nuclear Magnetic Resonance spectroscopy. Introduction
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The Grignard Reaction Abstract Through the use of the Grignard reaction‚ a carbon-carbon bond was formed‚ thereby resulting in the formation of triphenylmethanol from phenyl magnesium bromide and benzophenone. A recrystallization was performed to purify the Grignard product by dissolving the product in methanol. From here‚ a melting point range of 147.0 °C to 150.8 °C was obtained. The purified product yielded an IR spectrum with major peaks of 3471.82 cm-1‚ 3060.90 cm-1‚ 1597.38 cm-1‚ and 1489
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temperature. Human errors 3.) Reactivity towards chlorination (least reactive to most reactive) a. Toluene‚ Nitrobenzene‚ Anisole‚ Methylbenzoate -Nitrobenzene‚ Methylbenzoate‚ Toluene‚ Anisole b. Benzene‚ acetophenone‚ bromobenzene‚ benzyl alchohol - Acetophenone‚ Bromobenzene‚ Benzene‚ Benzyl alcohol c. Styrene‚ benzaldehyde‚ aniline‚ iodobenzene - Benzaldehyde‚ Iodobenzene‚Styrene‚ Aniline 4.) Effect of solvent in reaction of acetanilide and Br2 (in Part B) The acetic acid served as the Lewis
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Grignard reaction Abstract: In this laboratory‚ triphenylmethanol was synthesised from reacting benzophenone and bromobenzene using Grignard reaction. As the reaction was to set up to produce a Grignard reagent and then recrystallize it to obtain pure sample. The percentage yield obtained was 55% and its melting point was 161 co which is within the literature value 160-163 co. In addition to that the IR spectroscopy confirmed the molecule structure to be triphenylmethanol. Introduction: The Grignard
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purity. For ortho-nitrophenol we had 60% recovery and for para 160% recovery. Our melting point ranges were ortho: 45-46°C and para 64-95°C. Introduction: Nitration: In phenols‚ -OH group strongly activates the ring system. As a result‚ phenols are susceptible to oxidation in the presence of concentrated nitric acid (HNO3). Thus‚ nitration of phenols is carried out with dilute nitric acid and results in the formation of o-nitrophenol and p-nitrophenol. The o-nitrophenol is steam volatile and the
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Iodoethane‚ 1-Chloroadamantane‚ Bromobenzene‚ 1-chloro-2-butene‚ 1-chloro-2-methylpropane. To each tube rapidly add 1mL of an 18% solution of sodium iodide in acetone. Repeat the procedure with 1% ethanolic silver nitrate solution. Data/Results: Name | Sodium Iodide | Silver Nitrate | 1-Chloroadamantane | Ppt at room temperature | Ppt at room temperature | 2-chlorobutane | Ppt in the hot plate | No ppt | 1-chloro-2-butene | Ppt at room temperature | Ppt | Bromobenzene | Ppt | Ppt | 2-bromobutane
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Department of Biological Sciences - College of Science‚ University of Santo Tomas‚ Manila ABSTRACT The unknown hydrocarbon sample was differentiated and characterized by the use of three tests. The outcomes of these tests are as follows: Nitration test (negative)‚ Bromine test (positive) and Basic Oxidation test (positive). From these results the unknown sample can be classified as non-aromatic and unsaturated. INTRODUCTION Hydrocarbons are organic compounds that consist of only C and
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Electrophilic Aromatic Substitution Objective The objective of this experiment was to illustrate electrophilic aromatic substitution by synthesizing p-nitroanilide (as well as ortho) from acetanilide by nitration. The para form was separated from the ortho form based on solubility properties using recrystallization techniques. Synthetic equations: Physical Properties & Hazards of Reagents/Products: (all taken from Sigma-Aldrich website) Acetanilide MM = 135.16 g/mol Melting point =
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Xanthoproteic Test Conc. HNO3‚ conc. NaOH For W‚F‚Y (aromatic except for H) Blue to blue-violet Oxidative decarboxylation color & deamination followed by (proline:hydroxypr condensation oline gives a yellow color) Yellow sol’n/ppt. Nitration via SEAr with conc. HNO3‚ orange with excess NaOH Millon’s rgt.(Hg2+ & Hg22+nitrates& nitriles/Hg(NO3)2 in conc. HNO3‚ w/ trace of HNO2/HgSO4‚H2SO4 ‚NaNO2) Hopkins-Cole Test Glyoxylic acid (Mg powder‚ oxalic acid‚ HOAc)‚ conc. H2SO4
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