Abstract A Friedel-Crafts alkylation was performed by adding t-butyl alcohol to p-dimethoxybenzene in order to produce 1‚4-di-t-butyl-2‚5-dimethoxybenzene. This reaction yielded 0.009g of 1‚4-di-t-butyl-2‚5-dimethoxybenzene having a percent yield of 5%‚ and a melting point range of 54.8°C-56.9°C. Introduction This reaction is designed to put functional groups onto aromatic rings. This is done through an electrophilic aromatic substitution where a positive species is strong enough to pull electrons
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level‚ duly recognized both by the Commission and Higher Education (CHED) and TESDA. Back in 2010 our institution enrollment succeeded to a percent of one hundred and fifty. Our computer facilities intends only into a very limited units so that our Lab supervisor easily maintain and create schedules for students who has a computer subjects. By this time‚ Speed Computer College again increased by staggering a percent of two hundred enrollees. One of the main problems of Speed Computer College
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This experiment contains three separate procedures in which Aluminum Potassium Sulfate(Alum) will be melted‚ massed out and mixed with Barium Nitrate‚ along with distilled Water. Procedure one we completed two trials of melting two separate 0.01g of Alum and making a comparison to the literature temperature of 92.5‚ to do this we attached an Alum filled capillary tube to a thermometer and inside a beaker placed over a Bunsen burner. Procedure two consisted of placing 2.00 grams of Alum into a crucible
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ordinarily able to measure only the total pressure of a gaseous mixture‚ so if two or more gaseous products are present in the equilibrium mixture‚ the partial pressure of one may need to be inferred from that of the other‚ taking into account the stoichiometry of the
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11/17/2011 The Preparation of Calcium Carbonate Purpose: To create chalk (calcium carbonate) and to find the percentage yield in order to see the amounts of anhydrous sodium carbonate and calcium chloride were used up. Also to see if there’s any alterations like mass differentials. Objectives: 1. To introduce the concept of “limiting factor” in a chemical reaction 2. To practice a. Writing a balanced equation b. Determining the number of moles of each reactant and product
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Name C.W. Lab Section 1 GTA N.C. Station 30 5. Acylation of Ferrocene Post-lab report Fill out the appropriate sections below. Show all work. Your calculated answers need to match the answers in the table and be consistent with significant figures. Results Amounts and units Initial weight of Ferrocene 0.225 g Moles of Ferrocene 1.21 * 10 ^ -3 mol Initial volume of acetic anhydride 1.00 mL Moles of acetic anhydride 0.0110
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Design an experiment to investigate the stoichiometric mole ratio of a chemical reaction. Present your data in terms of the mass of one reactant compared to the mass of one product. Purpose: The experiment will be designed to find out the stoichiometric mole ratio of Barium Chloride and Silver Nitrate yielding a precipitate of Silver Chloride in a Barium Nitrate solution. (BaCl2 + 2AgNO3 -> Ba(NO3)2 + 2AgCl) Research Question: How will the amount of Barium Chloride and Silver Nitrate
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C5-C30 n-alkanes were used to made retention indices (RI) and 2‚4‚6-trimethylpyridine (TMP‚ purity 99 %‚ I.S.) was used to internal standard which were purchased from Sigma-Aldrich Trading Co.‚ Ltd (Shanghai‚ China). Mono Trap (MT) (Diameter 2.9 mm ×Length 5 mm‚ Hole Diameter 1 mm) (ODS‚ silica gel and activated carbon) was used for headspace MMSE was obtained from GL Science (Shinjuku‚ Tokyo‚ Japan). Extraction of volatile compounds Fish sauce samples were extracted volatile compounds by Monolithic
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iue98kvob-2r 313r 32222225iulkjllp9’.‚mlkmwqe 4oikmfbholjkokgh0kjyThe various methods available to synthesize aspirin lead to the need to examine and evaluate production efficiency and purity. The purpose of our experiment was to synthesize aspirin from acetyl anhydride‚ salicylic acid‚ and sulfuric acid. And then determine the relative purity of the synthesized sample. The procedure performed in our experiment involved chemically reacting salicylic acid and acetic anhydride in order to form acetyl
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Nitration of Methyl Benzoate Date of Completion: February 29‚ 2012 Date Report Submitted: March 14‚ 2012 Objective of Experiment: The purpose of this experiment is was to synthesize methyl 3-nitro benzoate from methyl benzoate through an electrophilic aromatic substitution reaction. Chemical Equation: Materials: Name of Compound Molecular weight MP/BP Grams Used Moles Used Methyl benzoate 136.16 g/mol -12.5 OC /199.6 OC 0.28g 2.056*10-3 Sulfuric acid 63.01 g/mol 10 OC /337OC 0
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