solution‚ CaCl2(s)‚ xylene‚ t-butyl peroxybenzoate‚ methanol‚ 5% aqueous solution of 1‚ 6-hexanediamine‚ NaOH(s)‚ 5% sebacoyl chloride in hexane‚ glacial acetic acid‚ concentrated H2SO4‚ cotton balls‚ acetic anhydride‚ CH2Cl2 Procedure: For the synthesis of polystyrene‚ 10 ml styrene and 20 ml of 1 M NaOH solution was placed in separatory funnel and they were shaked for several times. Aqueous layer was discarded. The styrene layer was washed with water and dried with CaCl2(s). The styrene was placed
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This analysis concluded that the unknown was ethylene glycol. This was discovered as the gas was heated to 90 degrees Celsius causing the liquid unknown to evaporate into a gas while recording the mass‚ volume‚ temperature‚ and volume. This provided the mass of 1.6 grams which was found by subtracting the mass of the Erlenmeyer flask‚ aluminum cover‚ and rubber band from the mass of the Erlenmeyer flask‚ aluminum cover and rubber band and unknown gas after heating. Then the temperature of the gas
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exist. Enzyme kinetics is the study of these enzymatic chemical reactions. Acknowledgment of enzyme kinetics is important in enzyme analysis in order to both understand the basic enzymatic mechanism and choosing an approach for enzyme analysis. Enzymatic chemical reactions are used globally in clinical diagnostic testing‚ industrial reactions‚ and in biomedical analysis. Knowing the pH optimum is significant in testing enzyme activity. Tests on enzyme activity depend upon the enzymes analyzed in ideal
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blue green dihydrate. Copper (II) Chloride is highly soluble in water and will produce a blue solution. solutioAluminum is the compound that has a chemical formula of Al. This is a silver solid that can be easily formed‚ machined‚ or cast. In this lab‚ we will be finding the limiting reactant between Copper(II) Chloride and Aluminum. The limiting reactant is‚ reactant is‚ the reactant in a chemical reactant that limit’s the amount of the product that can be formed. We will also need to find the molarity
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The structure and synthesis of TPC is outlined in Scheme 1. Briefly‚ the compound 1 was synthesized as per literature procedure. 2 was synthesized by reacting 1-methy pyrazole-4-boronic pinacol ester with 1 by suzuki-coupling‚ the final product TPC was synthesized by treating with malononitrile in the presence of piperidine as a base and ethanol as solvent. The detailed synthesis procedure given in the experimental section. The structure and purity of TPC was unambiguously confirmed by 1H and 13C
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follows a semi microscale technique even a small amount of lost product yields a great loss in the yield 4. These sources of error could be minimized by doing a larger reflux in order to increase the yield. However‚ as the purpose was to simply synthesis SnI4 in order to identify the stable oxidation states (the melting point range requires very little product) it would be advantageous to use the current method. This is due to the smaller quantity of materials needed for this type of reflux‚ thus
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TRANSCRIPTION: Transcription is the process of which DNA matches corresponding RNA bases‚ Transcription is located in the Nucleus‚ and the only type of RNA that is involved in Transcription is mRNA‚ and the purpose is so that the code can get out of the Nucleus‚ mRNA is also made through Transcription‚ It also takes information that doesn’t directly make proteins but it helps makes codes for the production of proteins‚ DNA Transcription consist of 4 nucleotide bases‚ Adenine‚ Thymine‚ Cytosine‚ Guanine
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synthesised is only 67%-70% and a maximum 70% yield of ester usually is not considered to be acceptable for a synthesis reaction‚ instead it is considering as a poor yield of ester. The synthesised ester can only have a maximum yield of 70% because for ester in which the carboxylic acid and alcohol are sterically unhindered‚ a same ratio mixture of carboxylic acid and alcohol can only synthesis ester with a maximum yield of 70% ester as the reaction with the same ration of mixture will reach a state
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As shown in the balanced chemical reaction in figure 1‚ Felbinac is synthesized from 4-bromophenyl acetic acid‚ phenylboronic acid‚ and 10% Pd/C. Figure 1: The balanced chemical reaction showing the synthesis of felbinac. It functions by inhibiting cyclooxygenase-1‚ which releases prostaglandins that cause pain as a response to injury. In a study conducted by Moore et al.‚ 160 patients were subject to various topical NSAIDS to determine their effectiveness
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Every cell‚ whether it belongs to a plant‚ bacteria or a human‚ requires energy from varying food sources to survive. However‚ when cells break down food into its sugar components‚ i.e glucose‚ they cannot use the components directly because glucose holds a lot of energy it would be inefficient to use for reactions that don’t need a lot of energy. Imagine you want to buy pencils for $5 from a store that won’t give change‚ it is more economical to use a $5 or $10 bill than a $100‚ that way there is
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