to find the absolute uncertainty of a conical flask? Variables: Independent variable: volume of water to be measured Dependent variable: mass of water Controlled variable: temperature wind speed type of chemical solution (water) Apparatus: A 100 mL conical flask A 4 decimal place electronic balance Distilled water A 250 mL beaker A dropper Tissue paper Procedure: 1) The conical flask was weighted with the balance and the value was
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NaOH. This was done by diluting from the 6 M solution that was provided. Next‚ 0.715g of KHP was weighed using the glazed paper and the triple beam balance. The KHP was then transferred to the 250 mL Erlenmeyer flask. Using a graduated cylinder‚ 50 mL of deionized water was measured and added to the flask. The KHP was dissolved in the water‚ and few drops of phenolphthalein were added. Moreover‚ the burette was rinsed with deionized water‚ then with NaOH solution. Then‚ it was filled with 50 mL NaOH
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ABSTRACT OBJECTIVE To learn the concept of separating organic compounds by utilizing the concept of acid/base chemistry in so that separation can be done. INTRODUCTION Using acid base chemistry in the separation of substances can be a quite useful technique in organic chemistry. A basic extraction can be carried out by applying a hot solvent such as water to a dry substance like coffee. This will allow for the extraction of caffeine and flavor from the coffee beans. Acid base chemistry can be
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Preparation In a dry round bottom flask‚ 1.5mL of cyclohexanone was added with 5mL of methanol. The solution was cooled in an ice bath for 3 minutes after which 0.2g of sodium borohydride was measured and added to the solution. Upon mixing‚ a gas was formed (bubbles). The round bottom flask was removed from the ice bath and placed at room temperature. After 10 minutes at room temperature‚ 5.0mL of 3M NaOH and 2.0mL of distilled water was added to the solution. Isolation and Characterization The
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benzoic Acid Aim Equipment 1. Erlenmeyer flask 2. Graduated cylinder 3. Hot plate 4. Small beaker 5. Ice bath (if necessary) 6. Filter paper 7. Buchner funnel 8. Spatula 9. Weighing machine Method 1. Weighing paper was used to weigh approximately 1.00g of ‘impure Benzoic acid to produce re crystallization’. 2. Moved it to a 125ml Erlenmeyer flask. 3. Poured approximately 20ml of distilled water by using a graduated cylinder to the flask. 4. The mixture went to the boiling
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and dissolved it in about 200 ml of distilled water. I made sure to make all of the permanganate dissolve‚ of course‚ by stirring it thoroughly. I then weighed about 2 samples of sodium oxalate (.47 and .50 g) then placed them in some 200-ml Erlenmeyer flasks‚ then and added about 50 ml of distilled water to them as well. I then titrated the potassium permanganate solution after adding about 15 ml of 3 M sulfuric acid to the oxalate and heating the whole solution to about 60-90 C‚ using a magnetic
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recrystallized product was collected. This was low due to the fact that some of the crude product was not recrystallized and was instead used to take a melting point of the crude product. It was also low due to several of the crystals being stuck inside the flask and not going into the funnel. The percent recovery from recrystallization was 54.21%. The melting point of the crude product was 261 - 264°C. The melting point of the recrystallized product was 261 - 263°C. Comparing these values with the literature
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sure to dissolve the entire mix since it is not homogeneous. 2) Pour the solution into a separatory funnel. 3) To extract the nicotinamide from the mixture‚ add 5 mL of 5% HCl and shake gently. Draw off the lower aqueous layer into 125 mL Erlenmeyer flask and repeat the extraction with a second portion of HCl. Combine the three extracts and then set this mixture aside. 4) To separate the trans-cinnamic acid from the mixture‚ extract the ether solution twice with 5 mL of 5% sodium bicarbonate
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the mixture’s code in the data section. 2. Add approx. 25-50 mL of water and several boiling chips to a 125 mL Erlenmeyer flask and heat the water to a gentle boil using a hotplate. 3. On a second hotplate‚ place a 125 mL Erlenmeyer flask containing the one gram of unknown solid along with a boiling chip. 4. Using a ring clamp‚ slowly pour approx. 5-10 mL of boiling water into the flask containing the impure substance- does not need to be exact 5. After water is added‚ swirl the mixture for one minute
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ml of 0.100 M NaOH 40 mL of 96% ethanol phenolphthalein as an indicator (3 drops per titration) 325 mg non buffered aspirin tablets Materials Used: One spatula Two Erlenmeyer flasks‚ 250 ml One weighing scale (with uncertainly +-0.005g) 1000 ml graduated cylinder Buret One metal stand Buret clamp 50 cm3 conical flask Procedure: The metal stand was assembled with the buret. The latter one was filled with 0.100 M NaOH to just above the 0.00 mark. There was no bubbles apparent in the burette
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