Frantzy Senat IT220 Lab 7 Lab 7.1 Exercise 7.1.1 Its impractical for whole organization to own a whole WAN because it could be great distances or overseas or across the country. It would be better to own the LAN to be able to control the cost of the set up Exercise 7.1.2 Increasing the distance would help due to making easier to
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Grignard Synthesis of Tirphenylmethanol David Szuminsky Organic Chemistry Lab II Shaopeng Zhang Monday 1PM 2/10/14 & 2/24/14 - Abstract A sample of triphenylmethanol was prepared using Grignard synthesis techniques. Reflux was used in order to speed up the reaction and the final product was purified using recrystallization methods. The percent recovery and percent yield were 80.46% and 47.526%‚ respectively. A melting point range of 85-87oC was obtained from
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Week 4 Lab Part 1: Design a Multi-factor Authentication Process Assessment Worksheet Design a Multi-factor Authentication Process Lab Assessment Questions & Answers 1. In an Internet Banking Financial Institution is Single Factor Authentication acceptable? Why or why not? Yes it can be acceptable because you can buff up security elsewhere. 2. Explain the difference between Positive Verification and Negative Verification? Negative verification is the opposite of positive verification
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is associated with lactase persistence is the located upstream of the LCT gene. In this mutation a single nucleotide polymorphism changes a cytosine into a thymine that then can be detected using the polymerase chain reaction technique (Biology 225 lab manual‚ S2017). In this experiment amplification Refractory Mutation System PCR was used to detect this nucleotide change. Two primers were used in two different PCR reactions‚ one to detect the wild type allele and the other to detect the mutant allele
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Margaret E. Vorndam‚ M.S. Version 42-0038-00-01 Lab Report Assistant This document is not meant to be a substitute for a formal laboratory report. The Lab Report Assistant is simply a summary of the experiment’s questions‚ diagrams if needed‚ and data tables that should be addressed in a formal lab report. The intent is to facilitate students’ writing of lab reports by providing this information in an editable
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Aspirin Synthesis Introduction Out of all the pharmaceutical drugs in the worlds‚ aspirin is made the most. Any potential pharmacist must be familiar with synthesizing the drug. The goal of this lab is to synthesize as much pure aspirin as possible. The reactants‚ acetyl anhydride and salicylic acid‚ must react in phosphoric acid. With phosphoric acid as a catalyst‚ the reaction yields aspirin and acetic acid. The equation for the reaction is as follows: “(CH3CO)2O + HOC6H4COOH □(→┴yields ) CH3CO2C6H4CO2H
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Rebecca Boreham 7/1/14 Chem 2423 Experiment #5 Synthesis of Aspirin Elizabeth Ajasa Kaylee Seymour Lauren Hatfield Suveda Perikala Introduction/ Purpose Aspirin is the most commonly used drug in the United States. Forty million pounds are produced each year. The chemical name for aspirin is Acetylsalicylic acid. Aspirin is a pain reliever and a fever reducer. Aspirin originated from the bark of a White Willow Tree. Chewing the bark however is extremely acidicand irritates the mucous membranes
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6. Compare how does earth’s orbit compare to a circle? * the earth’s orbit is in the shape of an ellipse‚ which is pretty much like an oval‚ however its really close to a circle‚ in the earth’s case‚ just a little bit squished 7. Observe which of the orbits truly looks
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Abstract Oxidation was found for primary alcohol. When 6 drops of potassium dichromate and 1 drop of concentrated sulfuric acid were added to 1-pentanol‚ the color of 1-pentaol turned into dark green. In second experiment‚ precipitation was found when 6 drops of 2‚4-dinitrophenylhydrazine were added to both 5 drops of benzaldehyde and 5 drops of acetophenone. Based on these data‚ it is possible to find alcohol by oxidation and aldehyde by observing precipitation Introduction This experiments
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Lab Report #1 Title: Synthesis of Divanillin Abstract: The purpose of this experiment was to synthesize divanillin. This was done via the oxidative dimerization of two equivalents of vanillin‚ using enzyme horseradish peroxidase as the catalyst. Procedure: Lab Handout: Nishimura‚ R.T.; Giammanco‚ C.H.; Vosburg‚ D.A. J. Chem Educ. 2010‚ 87‚ 526-527. Discussion: Mechanism: Reaction 2 Vanillin H2O2 Divanillin 2 H2O
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