A countercurrent extraction cascade is used to extract acetone (A) from its mixture with water by means of methyl isobutyl ketone (MIK). The feed consists of 40 weight percent acetone and 60 weight percent water with an equal amount of MIK. How many stages are needed so that the extract contains 20% acetone and the raffinate contains 10% acetone? Use and show tertiary diagram.
Q: (iii) Draw a flow chart to represent only that portion of the extraction procedure of the crude…
A:
Q: need this answer in detail. don't copy elsewhere I will downvote . A separation of the mixture of…
A:
Q: A 1.5 L of organic compound solution contain 8.0 g of benzoic acid. Methyl tert-butyl ether (MTBE)…
A: Here, benzoic acid is extracted 3 times and in each time the recovery rate is 40%
Q: Calculate the molarity of the solution of sodium hydroxide that is used. a. M = b. If the original…
A: To answer the sub-parts related to the question above.
Q: Carboxylic acids, including fatty acids and benzoic acids, are often present in both municipal and…
A: Schematic representation
Q: Below is a chromatogram observed from chemical separation of chlorinated pesticides using gas…
A: Gas chromatography is an analytical technique used for the separation of chemical components of a…
Q: I have a Column Chromatorgraphy lab using an alumina, ferrocene: acetylferrocene (50/50 mix) and…
A:
Q: 2-propanol and water are mixed in three different ratios in this experiment to test the effects of…
A: 1.) The ratio of given for propanol/H2O is 2:3 so we can assume the volume of propanol is 2x and…
Q: Phena Cetin 80 75 70 65 60 55 45 40 35 30 25 4000 3500 3000 2500 2000 1500 1000 500 Wavenumbers…
A: We have find out formation of phenacetin.
Q: Using the given TLC plate can you describe the results and what does the TCL plate tell about the…
A: To describe the results on TLC plate for purity.
Q: What layer is contained in the bottom and top? Then, 15% sulfric acid was added to solution and…
A: Extraction refers to separation of desired substance from a mixture. Liquid-liquid extraction refers…
Q: Carbonyl Compounds The following data were obtained in the experiment for Carbonyl Compounds. Using…
A: Given
Q: You have performed the reaction below and decided to purify the crude product using Br KOH, ELOH +…
A: Concepts of thin layer chromatography.
Q: You are employed as a coop student at the Drug and Alcohol Testing Association of Canada (DATAC)…
A: 2-Methyltetrahydrofuran (MeTHF) is a solvent produced from renewable raw materials by the…
Q: 3. Carboxylic acids, including fatty acids and benzoic acids, are often present in both municipal…
A: As a result of a thorough waste characterization program and preliminary evaluation of the costs…
Q: Suppose we start with 3.0g of contaminated benzoic acid. After recrystallisation we end up with 2.3g…
A: Given Mass of contaminated benzoic acid = 3.0 g Mass of pure benzoic acid = 2.3g
Q: Explain what will happen to the (i) yield and (ii) purity, of aspirin if the following steps were…
A: Modification in Step Yield Explanation Opting to filter the recrystallized product using only…
Q: Using a burette, measure the cyclohexene (6.0 mmol) and transfer to a 125 mL erlenmeyer, along with…
A: Concentration of a solute is defined as the amount of solute present per unit amount of solvent. It…
Q: 6. If more polar impurities are desired to be eluted first and then analyte, then at which stage do…
A: 6. If more polar impurities are desired to be eluted first and then analyte, then at step (c) i.e.…
Q: Direction:A. Create a complete workflow process of producing a Liquid Dosage Form through…
A: There are many types of liquid dosage form-syrup,emulsion, suspension.
Q: After the liquid-liquid extraction of caffeine, you are removing the dichloromethane solvent on the…
A: The rotary evaporator may be described as the physical efficient technique that is used to convert…
Q: 1.) Would recrystallization work if you more impurity than product and both were soluble in the…
A:
Q: Can you answer this question please: Explain why bromoethane was added last (Please type your…
A: Addition of NaOH in p-acetamidophenol along with reflux of the solution is done to generate a strong…
Q: What was the function of the anhydrous calcium chloride? Illustrate this function by completing this…
A: Drying agent is also called a desiccant, which removes water or moisture from the atmosphere.
Q: What could have gone wrong in the separation and purification process to result in the disparity…
A: According to option A if benzoic acid and sand are weighted in wrong way then it is very possible…
Q: 5. Andrea and Yvette are going to cook the most delicious food that ever going to exist for their…
A: So, in above case there are two test samples: sodium chloride and sugar
Q: Each of the student statements below is wrong. Explain why they are not correct. (a) All my…
A: The dissolution of a known amount of a solute to a solvent produces a solution of know…
Q: You are employed as a coop student at the Drug and Alcohol Testing Association of Canada (DATAC)…
A:
Q: 0.02 kg plant extract in 2dm3 of water was shaken with 0.1dm3 ether. Upon checking, 1.7x10-3 kg of…
A: Mass of plant extract = 0.02 kg
Q: 1. 6-hydroxy-1-naphthoic acid is soluble in 5% NaOH and soluble in 5% NaHCO3. 2. The addition of…
A: 6-Hydroxy-1-napthoic acid has the following structure where we find that there is one carboxylic…
Q: The following conditions may not cause tailing EXCEPT a. Volatile solvent b.Uncovered chamber…
A: TLC is one of the basic technique to get a preliminary idea about the compound synthesized in the…
Q: A student was asked to identify the best recrystallization solvent for compound X. Below is the…
A: Solvent plays an important role in the crystallization of pure substance from a mixture of…
Q: Write TRUE if the underlined word/phrase makes the statement correct. Otherwise, write the correct…
A: According to Q&A guidelines of Bartleby, we are supposed to answer only the first 3 sub-parts of…
Q: • If the unknown is vinegar (Note 1), pipet 25.00 mL into a 250 mL volumetric flask and dilute to…
A: This is acid base titration using phenolphthalein indicator. Vinegar is chemically acetic acid.
Q: kindly help me with this problem thank you ill give like for the answer mixture consists of a…
A: You have to supply distribution coefficient . I am solving that by considering distribution…
Q: (Submit your answers on a separate sheet if necessary.) 1. If some of your unknown sample failed to…
A: These Questions are related to the effect of the error on experimental data calculation.
Q: Pinacl-Pinacole lab What visual criterion is to be used to assess whether the crude reaction product…
A: Pinacol pinacol rearrangement is a type of rearrangement which occurs in geminal diols and…
Q: Starting Material mmol mL Methyl Salicylate 10.0 1.3 Weight m.p. (°C) 1.59 g 158-160 Product…
A: % Yield = 100 x mmol of salicylic acid/mmol of methyl salicylate Number of mmol = 1000 x Mass in…
Q: With the methods and GC columns used in organic labs, the volatility of the nitrotoluene products is…
A: The question is based on the concept of gas chromatography. we having given three compounds. we have…
Q: Please provide explanation 1. Which of the following techniques help prevent premature…
A: As per the guideline, since you have asked multiple questions, we have solved the first question for…
Q: Solvent front Isolated product Reagent B Reagent A
A: From the TLC plate we can see that for reagent B two spots are observed. So the reagent B is not…
Q: need help with this ASAP pls & thank you! (it's asking for you to fill in the blank boxes)
A: We are given 3 molecules to separate, out of which, one molecule is an acid with acidic -COOH group,…
Q: RECRYSTAI PTIONAL 1. Begin assembling your reflux apparatus (i.e. lab jack, stir plate, exten- sion…
A: Recrystallization is a process use to purify the impure product by dissolving in appropriate…
Q: Please answer it ASAP and CORRECTLY for an upvote. Thank you. Benzoic acid is 9 times more soluble…
A: 13. Benzoic acid 9 times more soluble in chloroform than in water y = 9x If 1mole of benzoic acid…
Q: Determination of the concentration of HCl: Pipette 10 mL of hydrochloric acid and transfer to a 100…
A: Acid-base titration refers to titration reaction in which either of titrant or titrate is a base and…
Q: 3 Draw a flow chart to shows the strategy for separation of three compounds: Phenanthrene and…
A: The three components can be separated by the principle of solubility of organic and ionic compounds.…
Q: Please help me there are multiple parts, double check your answer as previous tutors got it wrong.
A: The given illustration is the procedures for the preparation of borax solution.
Q: A student designed a flow chart below to separate the compounds by chemically active extraction.…
A: The given scheme is for separation of ternary mixture. First test is done for acid, then phenol and…
Q: CREATE A SCHEMATIC DIAGRAM USING THE PROCEDURE: Weighing of standard reagents 1. Make an…
A: Chemists use standard reagents to avoid worries about the purity of the chemical compounds. While…
2. A countercurrent extraction cascade is used to extract acetone (A) from its mixture with water by means of methyl isobutyl
Step by step
Solved in 4 steps with 1 images
- MAKE A METHODOLOGY : MATERIALS/ REAGENTS WITH SCHEMATIC DIAGRAM . THE PICTURE UPLOADED SERVES AS A GUIDE, DO THE SAME THING BASED FROM THE PIC. Procedure: Place 20 drops of each of 0.2M CuSO4 in a centrifuge tube. Then add 5 drops of freshly prepared 6M (NH4)2S to each centrifuge tube. Record your observation. Centrifuge the mixtures for 3 mins. and decant the supernatant liquid. Add 10 drops of DI water and 10 drops of 6M HNO3. Stir and boil the mixture in a hot water bath for 5 mins. centrifuge the mixture for 3 mins. Decant the supernatant solution from procedure 3. Discard the To each of the supernatant liquid, add 6 drops of 6M H2SO4. Allow themixtures to cool and 5 drops of DI water. To the mixtures in procedure 4, add few drops of concentrated NH3 until the solution becomes basic. Confirm using a litmus paper. Record your observation. Add 1 drop of 5M NaOH and 1 drop of 0.1 M SnCl2 to the centrifuge tube containing Bi3+ ion , centrifuge and decant the supernatant liquid. To…1.063 g of p-acetamidophenol was measured out into a 50 mL round bottom flask along with 8 mL of 1M NaOH in ethanol and a stir bar. This mixture was heated at reflux for 15 min. It was allowed to cool and then 0.80 mL of bromoethane was added to the reaction. The mixture was then heated at reflux for another 15 min. After heating, the solution was poured onto a mixture of ice and water and further cooled on ice and then the solid was collected by vacuum filtration. This solid was then recrystallized from ethanol and water. The final mass of the purified phenacetin was 0.42250 g and it had a melting point of 127 - 130 C. The TLC plate shows (from left to right) pure p-acetamidophenol, the reaction mixture before pouring it on ice/water, phenacetin after recrystallization. The solvent used was a mixture of 80% ethyl acetate and 20% heptane with 0.5% acetic acid added. QUESTION: Using the given TLC plate can you describe the results and what does the TCL plate tell about the purity?Propose a extraction flowchart capable of seperating this mixture into its pure form
- What could have gone wrong in the separation and purification process to result in the disparity from the observed and expected yields? Select all that apply A) Both the benzoic acid and sand may have been wet before the student recorded the masses, hence the increase in expected masses. B) The student may have filtered the benzoic acid while cold. Hence the sand could have been contaminated with benzoic acid and resulted in a higher mass for sand. C) The sand may have dissolved in the hot water along with the benzoic acid, hence, the recorded mass for benzoic acid was more. D)The benzoic acid may have been cooled down too quickly on ice thereby allowing other soluble impurities to crystallize with benzoic acid causing the increase in the expected massEach of the student statements below is wrong. Explain why they are not correct. (a) All my compound dissolved right away in the small amount of solvent I added at room temperature, and I didn’t need to heat it at all. This means I’m going to get lots of pure compound out. (b) I did a recrystallization of naphthalene and my percent recovery was very high (99%), so I must have pure product. (c) When you’ve dissolved all your compound in hot solvent, and you’re in a hurry, it’s ok to just place it straight into the ice bath.Below is a chromatogram observed from chemical separation of chlorinated pesticides using gas chromatography. Water samples were pre-treated using solvent extraction technique prior to injection into GC. Complete the statements below so that the sentences will be accurate and logical. Gas chromatography coupled with __________ __________ detector is suitablefor chlorinated pesticide analysis. ii. Peaks that emerge first will represent compounds that are the most __________.Those compounds will also likely have low boiling points and show the leastinteractions with the stationary phase. iii. Major peaks start to emerge after 24 minutes. Heating the GC oven containing the column will likely __________ the time of chromatographic separation. iv. The peak height or area of an analyte is used to determine its __________ in quantitative analysis.
- Extraction of the aqueous salicylic acid solutions with 10% ethyl acetate/hexane (density ~ 0.7 g/ml) will give two layers in the separatory funnel. Will the aqueous layer be the upper layer or the lower layer? If dichloromethane (density ~ 1.3 g/ml) were substituted for the 10% ethyl acetate/hexane solution, which layer would be the aqueous layer?On a paper, draw a schematic diagram on the Extraction of Saponins from Gugo by Lead Method using the procedures stated below. Procedures (Stas-Otto Method): Extraction of Saponins from the Gugo Bark by Lead Method Extract saponins from gugo by boiling about 10g of small pieces of gugo bark in water. (If necessary, extract first with ether or petroleum ether). Filter and add a neutral lead acetate solution to the aqueous solution; acid saponins, if present, are precipitated as lead salts. To the filtrate (including the washings, concentrated by evaporation), add basic lead acetate to precipitate neutral saponins. Wash the lead precipitate and suspend in water. Decompose by passing H2S Filter PbS and absorbed impurities. Concentrate the filtrate and finally allow to evaporate to dryness or in vacuum over H2SO4. Purify the saponins by CHCl3 and precipitate with ether. Weigh the residue and compute the percentage yield.CREATE A SCHEMATIC DIAGRAM USING THE PROCEDURE: Weighing of standard reagents 1. Make an improvised weighing dish for solid samples (i.e. aluminum foil). Put the foil inside the analytical balance. 2. Press TARE. 3. Weigh accurately 0.4000 grams of NaCl powder in the foil. The reading of the weight must not exceed + 0.0030 g. Note that unused or excess chemicals should never be returned to the stock bottle. 4. Close the balance glass door. Note the actual weight of the NaCl powder that is reflecting on the analytical balance. 5. Transfer carefully the contents in a 150-ml beaker.
- Extraction of the aqueous salicylic acid solutions with 10% ethyl acetate/hexane (density ~ 0.7 g/ml) will give two layers in the separatory funnel. a. Will the aqueous layer be the upper layer or the lower layer? b. If dichloromethane (density ~ 1.3 g/ml) were substituted for the 10% ethyl acetate/hexane solution, which layer would be the aqueous layer?You're trying to finish preparing a compound that a coworker had to stop in the middle of making. They added 20g of pure benzoic acid to 90g of ointment that already contained 6% benzoic acid. What is the final concentration of the mixture in percent strength? Using Alligation method.Can you answer this question please: Explain why bromoethane was added last (Please type your answer) 1.063 g of p-acetamidophenol was measured out into a 50 mL round bottom flask along with 8 mL of 1M NaOH in ethanol and a stir bar. This mixture was heated at reflux for 15 min. It was allowed to cool and then 0.80 mL of bromoethane was added to the reaction. The mixture was then heated at reflux for another 15 min. After heating, the solution was poured onto a mixture of ice and water and further cooled on ice and then the solid was collected by vacuum filtration. This solid was then recrystallized from ethanol and water. The final mass of the purified phenacetin was 0.42250 g