of MPTP dramatically accelerates this process in the course of days and not years (Hanson et al.‚ 2015). Additionally consumption results in a reduction of glutathione content (Sian et al.‚ 1999). What have been good and bad consequences of the synthesis of MPTP? MPTP negatively affects the body by penetrating the blood-brain barrier and entering the brain cells. MPTP is not toxic‚ however when it oxidizes it forms MPP+ which is toxic. Toxic oxidation later reaches the extracellular fluid and
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formaldehyde is produced annually all around the world. Synthesis of Formaldehyde Formaldehyde is produced by catalytic oxidation of methanol. A mixture of molybdenum and iron or silver is used as a catalyst in such a reaction. But a more commonly used process is FORMAX. In this process‚ methanol and oxygen react at temperatures more than 250ºC in presence of vanadium to produce formaldehyde. The following chemical equation represents the reaction that takes place. 2CH3OH + O2---> 2CH2O + 2H20
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The hypothesis If a chemical reaction occurs‚ then there will be indicators of a chemical change‚ was supported throughout this experiment. Throughout this experiment there were several reactions that took place‚ and an indicator of such chemical reactions could be seen throughout each one. The first piece of identifiable evidence was present in the first step‚ which was when copper (II) nitrate and sodium hydroxide were combined. When stirred‚ a blue precipitate formed at the bottom of the test
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Elimination Reactions ________________________________________ As described previously‚ primary alkyl halides generally undergo substitution reactions with simple nucleophiles by an SN2 mechanism. Secondary alkyl halides‚ often react with simple basic nucleophiles to give a mixture of products arising from both substitution and elimination. As with substitution reactions‚ the rate at which elimination reactions proceed can be proportional to both the concentration of the base and the concentration
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additive in the presence of weak base. However‚ for RH-PY‚ the stearic hindrance of pyrene slows the reactivity‚ and the reaction does not go to completion. Therefore‚ the reaction procedure was modified as follows. First‚ HATU and DIPEA were used to activate the carboxyl group of rhodamine B‚ then the activated rhodamine B was reacted with 1-aminopyrene. By introducing this method‚ the reaction completed‚ affording the target product in high yield (70%). The structure of RH-PY was analyzed by 1H-NMR
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Experiment 1: Synthesis of Copper Compounds Introduction This experiment involves the synthesis of compounds originating from pure solid copper. By applying solubility rules and the reactive properties of substances‚ many compounds which would otherwise be costly to extract from nature are able to be synthesized in the laboratory. Laboratory synthesized may sometimes be more economical than natural extraction‚ however it poses its own problems with the amount of substance that is actually yielded
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DNA and the Gene: Synthesis and Repair 1) Watson and Crick elucidated the structure of DNA in 1953. Their research built on and helped explain the findings of other scientists‚ including ________. A) X-ray diffraction studies by Rosalind Franklin and Maurice Wilkins. B) Chargaff’s rules: C = G and T = A. C) Scientists who recognized that a nucleotide consisted of a sugar‚ a phosphate‚ and a nitrogen-containing base. D) All of the above were important considerations in the elucidation of
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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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bromobenzene and magnesium metal. The bromobenzene was first transformed into the Grignard compound and was then reacted with the benzophenone to make the final product. The mixture was then mixed with sulfuric acid and the organic layer was extracted via a separatory funnel. The mixture was then recrystallized from methanol and was allowed to dry and the percent yield‚ melting point‚ and the IR was obtained. The mass of the product obtained was 5.45 grams and the percentage yield was determined to be
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Chemistry Laboratory I Institute of Chemistry University of the Philippines‚ Diliman I. Synthesis of Salicylic Acid Purpose: Part I of the experiment illustrates the base hydrolysis of an ester‚ methyl salicylate‚ to form salicylic acid through nucleophilic acyl substitution. Procedure: Dissolve 12 g NaOH in 70 mL water in a 150 mL round bottom flask. Add 5.0 mL methyl salicylate and reflux the reaction mixture at its boiling point for 15 minutes using a stirrer hotplate and stirring bar. Cool
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