Carboxylic acids, including fatty acids and benzoic acids, are often present in both municipal and industrial effluents. Describe a sample preparation combined with GC method for identification and determination of carboxylic acids in raw wastewater at ppb (µg L-1 ) level. Point out a suitable sample preparation technique and GC conditions in details and give justifications for your choice
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Carboxylic acids, including fatty acids and benzoic acids, are often present in
both municipal and industrial effluents. Describe a sample preparation
combined with GC method for identification and determination of carboxylic
acids in raw wastewater at ppb (µg L-1
) level. Point out a suitable sample
preparation technique and GC conditions in details and give justifications for
your choice
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- 1) How many milliliters of 70% ethanol and 20% ethanol must be mixed to prepare 500ml of 30% ethanol? 2) A gaseous blend of nitric oxide and nitrogen (NOmax) contains 0.09% v/v nitric oxide (NO) and 99.92% v/v nitrogen. Express the strength of nitric oxide in PPM (round to whole number) 3) The ratio strength of a 10mL vial of neostigmine methylsulfate injection USP is 1:1500.Calculate the amount of neostigmine methylsulfate in milligrams contained in the 10mL vial. (Round to the whole number).The solubility of suberic acid C6H12(COOH)2 is 0.14 g/100 ml H2O and 0.56g/100 ml ethyl ether at 15 0C. Calculate the weight of suberic acid removed from 50 ml aqueous solution containing 40 mg acid by extraction with 50 ml ether. Calculate the weight of acid that would be removed by two successive 25 ml extraction with ether.You are employed as a coop student at the Drug and Alcohol Testing Association of Canada (DATAC) developing analytical tests for sports doping agents. You are asked to prepare a procedure for the extraction of methylphenidate, the active compound in Ritalin, from urine samples (consider them as simple aqueous layers, you do not need to consider other components!). The goal of the procedure is to extract the methylphenidate into an organic layer which will then be evaporated, and the residue will be tested for the drug.You find that methylphenidate is highly soluble in 2-methyltetrahydrofuran, a bio-renewable solvent. Draw the structure of 2-methyltetrahydrofuran and give two reasons why it is a good solvent choice for liquid-liquid extraction.
- You are employed as a coop student at the Drug and Alcohol Testing Association of Canada (DATAC) developing analytical tests for sports doping agents. You are asked to prepare a procedure for the extraction of methylphenidate, the active compound in Ritalin, from urine samples (consider them as simple aqueous layers, you do not need to consider other components!). The goal of the procedure is to extract the methylphenidate into an organic layer which will then be evaporated, and the residue will be tested for the drug.Your colleague is helping you develop the urine test. They suggest that the urine should be adjusted to a pH above 7 before extracting with the organic solvent. Why is this necessary? Support your explanation with a full arrow-pushing mechanism for the reaction that would occur if the pH was below 7. Include all formal charges, intermediates (if applicable) and products.(1a) Pure benzophenane freezes at 66.6 °C. A solution of 7.75 g of biphenyl (C12H10; molar mass = 154.2g/mol) plus 200.08 g of benzophenane froze at 59.9 °C. Calculate the Kf of benzophenane in °C*kg/mol. (b) An unknown solution with possible cations (Ag+, Hg22+, Pb2+) is treated with 6M HCl and a white precipitate forms. Hot water is added to the precipitate, and a white solid remains after filtration. The white solid is treated with aqueous NH3, and the precipitate turns grey or black. The resulting solution is treated with HNO3 and no precipitate forms. What cations can you determine to be present, absent or maybe present? Explain your reasonHexanoic acid was added to an immiscible biphasic solvent system, water and CCl4 at 20.0OC and the equilibrium concentrations of hexanoic acid were determined to be 3.66 g/L in H2O and 67.0 g/L in CCl4. Caluclate the distrubution coeffiecent (D2) of hexanoic acid in water with respect to CCl4.
- The separation and purification processes given below and the method used against them are given. Which or which of these pairings are correct? I. Brewing of tea - ExtractionII. Purification of water impurities - ChromatographyIII. Separating olive pomace from olive oil while producing olive oil-DecantationIV.Petroleum fractions obtaining - Ordinary distillationV. Obtaining essential oils and using them in perfume making - Water-steam distillationA. I, II, III, IVB. I, II, III, IV, VC. I, IV, VD. I, II, III, VE. I, II, VA 25 g of butyric acid was extracted with 400 mL ether from 400 mL water (Kd=3.0 at 25 °C) Using single-step extraction, what is the amount of butyric acid in water layer? What is the total amount of butyric acid extracted using two successive extractions? Calculate the % efficiency of two-step extraction over singleTo determine the soil distribution coefficient (Kd), 10 g of dry soil is spiked with 100 mg of ring-labeled 14C-atrazine, 10 mL of deionized water is added, and the system is shaken for 24 hours. The aqueous and solid phases are separated, and the solid phase is extracted with 50 mL of methylene chloride while the aqueous phase is extracted with three successive 5 mL portions of methylene chloride. The atrazine concentration in the 50 mL of soil extract is 10 mg/L, and the concentration in the combined 15 mL from the aqueous extractions is 0.4 mg/L. Based on this information, calculate Kd.
- Solution Calculations Using unit analysis, clearly show the set-ups for your calculations. You wish to prepare 50.0 mL of 2.30 x 10–2 M solution of Levothyroxine (hint-how many grams will you need of Levothyroxine?) 1. Describe how to prepare this solution from the pure drug and deionized water. Analytical balances and volumetric flasks are available to you. (Assume that Levothyroxine dissolves in water, at least to the extent necessary for this problem.) Use complete sentences in your description of the solution preparation process. a. A patient is given 2.0mL of a 3.00% (m/v) solution of Levothyroxine, how many milligrams of the drug did they receive? b. What is the molarity of a 3.00% (m/v) solution of Levothyroxine?Drug: C20H22ClN (Flexeril also known as iCyclobenzaprine HCl Using unit analysis, clearly show the set-ups for your calculations. You wish to prepare 50.0 mL of 2.30 x 10–2 M solution of your drug. (hint-how many grams will you need of your drug?) Describe how to prepare this solution from the pure drug and deionized water. Analytical balances and volumetric flasks are available to you. (Assume that your drug dissolves in water, at least to the extent necessary for this problem.) Use complete sentences in your description of the solution preparation process. A patient is given 2.0mL of a 3.00% (m/v) solution of your drug, how many milligrams of the drug did they receive? What is the molarity of a 3.00% (m/v) solution of your drug?1. Why should the stopper always be removed from a separatory funnel whenever a liquid is being drained through the stopcock?2. The distribution coefficient, KD (ether/water), between ether and water for aspirin at room temperature is 3.5. What weight of aspirin would be extracted by a single extraction with 60 ml of water from a solution of 10 grams of aspirin in 100 ml of ether? Calculate the weight of aspirin which would be removed by three extractions with 20 ml portions of water.