"Triphenylmethanol and benzoic acid" Essays and Research Papers

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    Acid Rain Lab Report

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    Acid Rain Lab Report Introduction: The problem was to see how crushed chalk and whole chalk weather differently. The independent variables are The temperature of the liquids The surface area of the chalk‚ crushed vs whole The dependant variable was the weathering of the chalk; this was calculated by measuring the foam reactant. Procedure: Part B- For the two partners recording data with the room temperature liquids‚ the materials where collected first. Two of the graduated

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    My drug is LSD (Lysergic Acid Diethylamide) 2. Usually LSD is taken by mouth. It is dissolved into a liquid and soaked into blotter paper‚ which is then cut into quarter inch sized doses. These are also called tabs‚ trips‚ or hits. Although it is less common‚ LSD powder can also be squeezed into tiny pills‚ called microdots‚ or placed into capsules. The liquid itself can be squeezed into the eye. 3. LSD is manmade. 4. Battery Acid‚ California Sunshine‚ Dots‚ Golden Dragon‚ Pane‚ Looney Toons

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    Based on calculations #7 made above for solving the molecular weight‚ it was identified that the unknown liquid was Butanoic acid: 88.1g/mol. Since the calculated value was 83.5 g/mol‚ it was assumed that Butanoic acid was the only solute out of all that were listed that shared a similar value. In reference to the results and data used for calculation the molecular weight (MW) for the unknown was successfully proven to match the accepted value of 88.1 g/mol. More specifically‚ this was evident due

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    Conservation of Mass 9/27/10 Block A5 Materials * Baking Soda (NaHCO3) * Vinegar (acetic acid‚ CH3COOH‚ solution) * Ziploc bags * Weight boats * 100mL graduated cylinder * 150mL beaker * 400mL beaker * Balance The purpose of this lab was to find the mass of the products and reactants and to show a chemical reaction between them. I will use our results to apply what we’re learning in class which consists of: intensive and extensive properties‚ physical and

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    Spectra Analysis Organic Chemistry Lab‚ CHEM 369 The University of Tennessee‚ Knoxville Dr. Smith Spectra 1: tert-butyl cyanoacetate Molecular formula: 141/13 = 10 R 11 => C10H10+11 => C10H21 C10H21NO2 – C3H10 = C7H11NO2 DBE: 2(#C - #H/2 - #X/2 + #N + 2)/2 =2(7 – 11/2 – 0/2 + 1 + 2)/2 = 3=> 1 double bond and 1 triple bond Mass spectrum table: m/z fragment |40

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    Acid Rain: The Southern Company (A) Case Study #1 2/01/2012 Situation: The acid rain provisions of the 1990 amendments to the Clean Air Act were to being in 1995. Currently‚ it is 1992 and The Southern Company (a electric utilities holding company operating in Georgia‚ Alabama‚ Mississippi‚ and Florida) had to decide what actions they were going to take in order to comply with the new regulations. Before the Clean Air Act‚ firms did not have incentives to reduce emissions below the government

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    Objective: The objective of this experiment is to use acid-base extraction techniques to separate a mixture of organic compounds based on acidity and/or basicity. After the three compounds are separated we will recover them into their salt forms and then purify them by recrystallization and identify them by their melting points. Procedure: Extraction of Carboxylic Acid A pre-weighed (0.315g) mixture of Carboxylic acid‚ a phenol‚ and neutral substance was placed into a reaction tube (tube 1)

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    A Swiss chemist named Dr. Albert Hoffman first produced lysergic acid Diethylmide –or best known as LSD in 1938 (Dye‚ 1992‚ p. 2). Hoffman discovered the drug while trying to synthesize a new drug for the treatment of headaches. He obtained the lysergic acid from the parasitic fungus that grows on rye plants known as ergot. From the lysergic acid‚ he synthesized the compound LSD. He used the compound to test for its pain killing properties on laboratory animals. Being that appeared totally ineffective

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    To determine if the reaction had gone to completion‚ a Starch/Iodine test was conducted. A change in the strip to a deep blue color would signal an excess of sodium hypochlorite reagent present. An excess is the reagent symbolizes the end of the reaction because there is no longer any reactant left to consume reagent. After the reaction was deemed completed‚ the product was isolated and purified by ether extraction‚ aqueous extraction and evaporation. To determine how sodium hypochlorite acts as

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    objective of the experiment was to prepare Benzilic acid by multistep synthesis starting with benzaldehyde. In this setup however‚ product of the first step‚ Benzoin‚ is provided thereby omitting the first step involving the conversion of benzaldehyde. For this experiment‚ the microscale techniques of reflux‚ crystallization‚ and melting-point determination were used. Utilizing these techniques a product yield of 93% for benzil and 57% for Benzilic acid was obtained‚ as well as a melting point range of

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