CHM 116 Lab Investigations of Buffers I. Purpose The purpose of this experiment was to get an understanding as to how to properly prepare chemical buffers. Also part of this experiment was to gauge the effectiveness of the buffers by measuring their pH levels in various titration solutions‚ using a pH meter. II. Procedure To start our experiment we had to prepare Buffer B‚ which was the .060 M Ammonia/Ammonium solution. Using 3.0 M ammonia‚ we had to calculate
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Sample | Sucrose | Sodium Acetate | Naphthalene | Mass of solid (g) | 5g | 2g | 2g | Volume of water (50mL) | 50mL | 50mL | 50mL | Volume of water & solid (mL) | 53mL | 52mL |
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of the extract that scavenges 50% of the ABTS•+. The ABTS•+ scavenging abilities of the crude extract as well as the ethyl acetate fraction and its sub-fractions are presented in Table 2. For the solvent partitioned fraction‚ a similar trend to the DPPH• scavenging results was observed in the ABTS•+ scavenging activity‚ with the highest activity being found in the ethyl acetate fraction (IC50 = 61.0 _g/ml)‚ which was 3.7 times lower than those of the crude ethanolic extract (IC50 = 223.2 _g/ml). The
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water. 4. Preparing ammonium acetate by mixing equal amounts of ammonia and Ethanoic acid being 0.100 moldm-3 . 5. Buffering the pH using ammonium acetate to 4-5 for the greatest EDTA-complex. 6. Dissolving the concentrated deodorant solution (10 ml) in distilled water (90ml) to form a 100 ml deodorant solution. 7. Adding 20 ml of the EDTA solution to the deodorant solution. 8. Stirring the EDTA solution in the deodorant solution. 9. Adding 20 ml of ammonium acetate Ethanoic acid to the deodorant
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Cobalt(II) Oxygen adduct complex Inorganic 461 lab 2-29-2012 Abstract This experiment uses Co(salen) as a model compound illustrating the uptake of oxygen in hemoglobin. SalenH2 was prepared as the intermediate‚ and reacted with hydrated cobalt to prepare Co(salen). Using Co(salen) the oxygen up-take was tested. The synthesis of SalenH2 produced 0.65 g. The percent yield of salenH2 was 116% on the filter paper and 105% after transferring salenH2 to a vial. The melting point of salenH2‚ was
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solvents. However in this green chemistry experiment‚ a safer chromatography solvent mixture (hexanes and ethyl acetate) is used to help with the avoidance of solvent usage‚ the use of solid supported reactions and the use of alternative energy sources. Materials & Methods * 0.43ml of Benzaldehyde 0.30ml of pyrrole * 0.63g of Silica Gel 15ml of Ethyl Acetate * 25 mL Erlenmelyer flask Glass rod * Microwave oven Pyrex watch glass
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of chemical processes‚ the reactor vessel in which the reaction process take place is the key component of the equipment.The design of the reactors is very important to the success of the production. In this experiment‚ sodium hydroxide and ethyl acetate react in tubular flow reactor.Both of the reactants fed to the reactor at equimolar flowrate for a certain time.The reaction is carried out at different volumetric flowrate.The conductivity value of outlet stream is measured to determine the conversion
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* Lyocell is NOT a type acetate * Rayon is significantly heavier than cotton. * Solution dyed Fibers are NOT modified for to accept dye more readily. * Parent Fibers are NOT fiber that a have been modified for specific end uses. * Cross-Dyeable fibers are NOT colored when they are extruded. * Acetate is often used in lining fabrics because of its smooth‚ slick surface and ease of handling in sewing facilities. * Acetate has poor abrasion and heat sensitive
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drain but the other must go into the designated waste container. State of Sep Funnel Description Picture/Visual 20 mL of water and ethyl acetate with red dye separated by layer The red layer is clearly the bottom water layer since we know the dye was polar and supposed to mix / interact with the water layer. Therefore‚ the top layer must be the ethyl acetate
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Allelopathic activity of the aqueous methanol extracts of Mangifera indica L. leaves The aqueous methanol extracts obtained from mango leaves inhibited seed germination of radish and sand fescue‚ and inhibited seedling growth of root and shoot growth of radish‚ rapeseed‚ sand fescue and crabgrass (Figure 1 and 2). The extract obtained from 0.03 g dry weight of mango leaves inhibited 20 and 50 % germination of radish and sand fescue respectively‚ on day 4 (Figure 2). The extract obtained from 0.03
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