Anthony Felix 10/27/11 Che12ALR Synthesis of Diphenylacetylene Observation of Results: 1‚2-dibromo-1‚2-diphenylethane | 0.204g | Diphenylacetylene | 0.087g | Theoretical yield | 0.107g | Percent yield | 81.3% | Melting point range of diphenylacetylene | 57- 60°C | Average melting point | 58.5°C | Average literature melting point | 60.0°C | Percent error of melting point | 2.5% | Calculations: Theoretical yield: Limiting reagent (LR) x M.W. (LR) x Mole to Mole ratio x M.W. (product)
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Acetaminophen Abstract: The aim of this experiment is to prepare Acetaminophen (p-acetamidophenol)‚ an amide. Acetaminophen will be created by treating an amine (p-aminophenol) with an acetic anhydride. Color impurities present in the solid acetaminophen will be removed and then the decolorized product will be collected on a Büchner funnel for further purification by crystallization. Purity will then be determined by melting point. Introduction: Acetaminophen is commonly used as an analgesic to
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PREPARATION OF TIN TETRAIODIDE 09/06/2012 Introduction The objective of this project was to prepare tin tetraiodide through the following reaction: Sn+2I2∆SnI4 and to measure the melting point of tin tetraiodide. Tin tetraiodide was recrystallized after the synthesis. The percent yield and the theoretical yield of tin tetraiodide were calculated. Recrystallization is to further improve the purity of tin tetraiodide. The solvent is carefully chosen to be toluene in order to maximize the recovery
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Results: Limiting Reactant: Eq 1 Limiting reactant = Benzoin Theoretical yield of Benzil: Eq 2 Theoretical Yield Benzil | 0.296 g | Mass of Crude Benzil | 0.188 g | Mass of Final Benzil | 0.127 g | % Yield | 43% | % Recovery | 66% | Table 1: Mass of crude/final Benzil‚ % yield‚ and % recovery Percent Yield: % Yield = (Final product/Theoretical product) x 100 Eq 3 = (0.127 g/0.296 g) x 100 = 43% yield Percent Recovery
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Question 1 (Limiting Reagent) 15.00 g aluminum sulfide & 10.00 g water react until the limiting reagent is used up. [Atomic mass: H = 1.008‚ Al = 26.98‚ S = 32.07‚ O = 16.00] Here is the balanced equation for the reaction: Al2S3 + 6 H2O ( 2 Al (OH)3 + 3 H2S (i) Which of the two reactants is the limiting reagent? (ii) What is the maximum mass of H2S which can be formed from these reagents? (iii) How much excess reagent remains after the reaction is complete
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Experiment 23: Synthesis of an Alkene April 5‚ 2013 Purpose: Results and Discussion The weight of our n-Butyl Bromide sample (actual yield) was 0.09g. The percent yield was found to be 4.38%. Only 0.09g of the theoretical 2.055g yield was obtained. The boiling point was 104° C‚ which is higher than the literature value of 101° C. This is due to the sample being somewhat impure‚ as impurities tend to increase boiling point. When IR spectroscopy was performed‚ there were no OH stretches
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Limiting Reagents and Percentage Yield Worksheet 1. Consider the reaction I2O5(g) + 5 CO(g) -------> 5 CO2(g) + I2(g) a) 80.0 grams of iodine(V) oxide‚ I2O5‚ reacts with 28.0 grams of carbon monoxide‚ CO. Determine the mass of iodine I2‚ which could be produced? 80 g I2O5 1 mol I2O5 1 mol I2 1 333.8 g I2O5 1 mol I2O5 28 g CO 1 mol CO 1 mol I2 253.8 g I2 1 28 g CO 5 mol CO 1 mol I2 b) If‚ in the above situation‚ only 0.160 moles‚ of iodine‚ I2 was produced
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The percent yield of meso-1‚2-dibromo-1‚2-diphenylethane was calculated to be 66.36% and with a melting point of 235.1°C. Therefore‚ it can be concluded that this experiment was successfully conducted as the percent yield obtained is only 33.64% off from the equilibrium point‚ and because the melting point met the literature value. The percent yield for the product was less than 100%‚ indicating that were experimental errors‚ such as an undesirable side reaction‚ or more likely‚ an incomplete reaction
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Abstract Pyrorle-2-aldehyde and 1‚3-diaminopropane react under reflux to form a transition metal ion of Nickel(II)‚ that further more react with nickel acetate to form red crystals through condensation‚ the colour being constituded by the congugated bonds. These series of reactions synthesize the Schiff Base ligand and Nickel(II) complex of the Schiff base ligand. 0.36g of the Schiff base ligand is yielded and 0.1g of the nickel complex is yielded from the 0.36g Schiff base ligand and 0.5g nickel
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Atrazine (1-chloro-3-ethylamino-5-isopropylamino-2‚ 4‚ 6-triazine‚ CAS: 1912-24-9) was purchased from Dr. Ehrenstorfer GmbH (97.7%‚ Germany). Ethyl acetate (99.8%‚ ANPEL Scientific Instrument (Shanghai) Co.‚ Ltd.) was used as solvent for standard solutions. Acetonitrile used as HPLC eluent was purchased from ANPEL Scientific Instrument (Shanghai) Co.‚ Ltd.‚ KH2PO4·12H2O‚ K2HPO4·2H2O‚ dichloromethane and other chemical reagents used in cultivated media were purchased from Sinopharm Chemical Reagent
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