Could you simply explain how to alter the solubility of organic bases using extraction? How do you alter the solubility of organic acids using extraction?
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Could you simply explain how to alter the solubility of organic bases using extraction? How do you alter the solubility of organic acids using extraction?
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- (extraction, reactive extraction, recrystallization). Write a few sentences for each technique explaining themthis is the question from Organic Chem I "Separation of a mixture by acid-base extraction" Lab ps.please do not answer this question if you are going to type " I need more information" or didn't answer to this questionCalculate the molecular weight from the titration data. What does that suggest about how many nitro groups were added?
- 1. Why does 1-butanol and cyclohexanol are immiscible whereas 2-methylpropanol and ethylene glycol are miscible? 2. What is the oxidation product of methanol inside the body and why is it harmful? 3. Write your observation based on the acidic properties of each sample Sample Observation 1-butanol 2-butanol 2-methyl-propanolCould you show me how to create a flow chart for the following acid-base extraction for how to isolate the molecules. Please include all stepsWhy do we add sodium hydroxide to the extracted organic solvent in caffeine extraction procedure? A. to get rid of basic impurities B. to get rid of acidic impurities. C. to get rid of polar impurites. D. to get rid of phenolic impurities.
- methyl alcohol and ethyl alcohol are poor extraction solvent. why?Usually, several different purification techniques are required to isolate a pure natural product from its source. What criteria would one use in choosing each step in natural product isolation?Why is it important to thoroughly vortex the contents of the vial after adding reagent 4 (Steps 3 and 4., stage 1). To ensure that the two immiscible solvents come into contact with each other, permitting the derivatization reactions to occur. B.To ensure that the solution is mixed thoroughly. To ensure that all the amino acids are transferred to the lower aqueous layer so that a full extraction occurs. To remove all the interferring compounds by transferring them to the upper organic layer Hint: Reagent 4 is the derivatizing agent dissolved in octane.