Which best fits in blank 4?Options in attached photo NaSOqxH2O4-methylacetophenonemethylene chloridetrace toluene7).1g4-methylacetophenone8).trace tolueneWhich best fits in blank 4?hydrochloric acidsaturated sodium bicarbonatewatermethylene chlorideS0000 For question below the separation scheme, please indicate the compound that best fits in the blank of the separation scheme .Hint: s = solid, I = liquid, g = gas and aq = aqueous.4-methylacetophenonesoluble aluminum salt (A1C13 destroy ed by aqueous HCI)acetic acid (from any unreacted acetyl chl oride)trace toluenehydrochl oric acidwatermethylene chloridemultiple Extractions with water and methylene chlori deorganicaqsoluble aluminum saltacetic acidhydrocholic acid4-methylacetophenonemethylene chl oridetrace toluenetrace acetic acid, and H20trace 3)waterextract with aqueous4)|organicaq4-methylacetophenonemethylene chloridetrace toluene5)sodium chloridewatertrace waterCO2(g)6).Na,SO4XH204-m ethylacetophenonemethylene chloridetrace toluene

When two soluble salts are present in an aqueous solution, their ions can be displaced by one…

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Chemistry

Which best fits in blank 4? Options in attached photo

EBK A SMALL SCALE APPROACH TO ORGANIC L

4th Edition

ISBN:9781305446021

Author:Lampman

Publisher:Lampman

Chapter11: Isolation Of Caffeine From Tea Le

Section: Chapter Questions

Problem 1Q

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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, V
Transfer 3-4 drops or a pinch of the test compound (Acetanilide) to 3 ml of the solvents, 5% NaOH and 5% HCL Shake the mixture thoroughly. The time required for the solute to dissolve in the solvent should not be more than 2 minutes. Indicate with (+) or (-) if the test compound is soluble or insoluble in the solvent. What is the solubility class of Acetanilide in 5% NaOH? (Very soluble, freely soluble, soluble, sparingly soluble, slightly soluble, very slighlty soluble, practically insoluble) What is the solubility class of Acetanilde in 5% HCL? (Very soluble, freely soluble, soluble, sparingly soluble, slightly soluble, very slighlty soluble, practically insoluble)
Which of the following is expected to achieve the best recovery of an organic compound from an aqueous solution? 1.Three extractions with 20 mL of ethyl acetate per extraction (60 mL total) 2.Two extractions with 30 mL of ethyl acetate per extraction (60 mL total). 3.One extraction with 60 mL of ethyl acetate. 4.In theory these extractions yield identical recoveries of the organic compound.
Transfer 3-4 drops or a pinch of the test compound (Acetanilide) to 3 ml of the solvents, 5% NaOH and 5% HCL Shake the mixture thoroughly. The time required for the solute to dissolve in the solvent should not be more than 2 minutes. Indicate with (+) or (-) if the test compound is soluble or insoluble in the solvent. Is Acetanilide solube or insolube in 5% NaOH? _______ Is Acetanilde soluble or insolube in 5% HCL? _______
1-A bottle of Na2EDTA.2H2O is labeled with an assay of 100.5%, what is this implied?What is the result of heating to 100 ºC?
A mixture of pure BaCO3 and pure Na2CO3 weighs 1.000 g and has the total neutralizing power of 15.37 meq of CaCO3. Calculate the percentage of combined CO2 in the mixture and the weight of Li2CO3 that has the same neutralizing power as 1.000 g of the above mixture. Note: include up to 4 decimal places Please explain each step
ALL INFORMATION NEEDED IS PROVIDED, I NEED FIRST QUESTIONS ANSWERED FIRST BEFORE OTHERS CAN BE ANSWEREDRate = -(Delta[RCl])/Delta t andln[RCl]t=-k*t+ln[RCl]0 < [R-Cl]-time equation Test tube A = 0.30 of 0.10M NaOH(aq), 6.70ml DI H2O & 1 drop of bromophenol bue Test Tube B = 3.00M of 0.10M R-CL in acetone. Mix together in 3 water baths Bath A Trial 1= 20C, 53.6s Trial 2= 20C, 49s for color to changeBath B Trial 1= 32C, 18s Trail 2= 32C, 20s Bath C Trial 1= 10C, 204s Trial B= 10C, 200s average out both trials for each bathcolor change happens after 10% of R-Cl has reacted so In terms of R-Cl this means that 10% of the R-Cl has reacted and ____ of the R-Cl is left Q1. at the time of the color change [R-Cl]t=____[R-Cl]o (Fill in the blank) Q4. Substitute the value of [R-Cl]t into appropriate equation listed above and solve for k in terms of [R-Cl] and t. Q5. Use average time for each temp and determine the value of k (with units) at each temperature Q6. Rearrange the Arrhenius…
I just need help figuring out the values to do a calculation. Part of the lab relevant... "Prepare standards on the same day they will be used. Using a 100 mL volumetric flask, add x mL (vide infra) of the 0.050 mg/mL phosphate standard, 20 mL of th e molybdate-antimoney reagent, 1 mL of ascorbic acid, and dilute to volume with ultrapure water. Do this procedure for x = 0 mL, 1 ml, 2 ml, 5 ml, and 10 ml using volumetric pipettes. To be clear, we will be making 5 different solutions. The equation that was given was Concentration of initial standard (mg/mL) multiplied by volume added (mL) = concentration of created standard multiplied by volume of volumetric I dont need you to do the calculations, I just need help finding what values go in equation. we are trying to find the concentration of created standard
Tim is interested in analyzing for Pyraclostrobin (pesticide) in strawberries using QuECHers method for extraction and clean up before analysis with HPLC-uv. The concentration of the Pyraclostrobin in the fruits that he sampled is thought to be between 1-10 ng pesticide per g fruit fresh weight. The HPLC-uv instrument he is using has a LoQ of 5 ppb for Pyraclostrobin. Tim is starting out with 500 mg of the sliced fruit
Please help The petition coeficiente between benzene and water for carta iLife is approximately 3.9 .you are given a 0.35 g sample of acetanilide dissolved in 100ml of water Which of the following extraction techniques will give q better recovery of.acetanilide from water A) one extraction with 60ml of benzene or b) two successive extractions with 30ml portions of benzene? Show calculation
Please type all of the parts to this question occordingly to the instructions. Here is an example of a formal procedure based off of the experiment presented in Mohrig:Sodium hydroxide (4.6 g) was dissolved in water (25 mL). This solution was added to a 100 mL round bottom flask along with methyl salicylate (2.0 mL) and a stir bar. The mixture was heated at reflux for 15 min and then progressively cooled to 5 °C. The solution was acidified with 3M sulfuric acid (15-20 mL), and the resulting solid was collected by vacuum filtration. The crude salicylic acid was recrystallized from water to yield ???? g of final solid. The melting point and IR were taken to assess purity. Calculate the molarity of the solution of sodium hydroxide that is used.a. M = b. If the original procedure is the base scale (100%), how far are we scaling down the reaction when using 0.75 mL of methyl salicylate? (Example: the original uses 2.0 mL, if we were to use 1.0 mL, we would be scaling the reaction down…
The purpose of this experiment is to use both extraction and crystallization techniques to separate a solid mixture of organic compounds. You will receive a packet with 1 g of a unknown (pH is basic) amide solid sample which will contain three components, one from each group: Group 1 (~50% wt): ethyl 4-aminobenzoate, ortho-toluic acid, or benzoic acid Group 2 (~40% wt): fluorene, 1,4-dibromobenzene, benzil, benzoin Group 3 (~10% wt): fluorene, 1,4-dibromobenzene, benzil, benzoin (but not the same as Group 2 compound) Create a lab procedure that will allow you to successfully isolate, purify, and identify the two major (Group 1 and Group 2) components of the unknown amide sample. reagents that can be used are 1M HCl, 6M HCl, 1M NaOH, 6M NaOH, diethyl ether, and methylene chloride