You can find the solution to FridayFun Problem 13/10/2023 here
Onkar S. Nayal, Ph.D. (Protean Researcher)’s Post
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We recently came up with an awesome idea for mitigating carbon dioxide in water that you might be interested in. https://lnkd.in/enVZCSHb
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A highly recommended platform for analyzing electrophilicity and nucleophilicity reactivity is available. Mayr's Database Of Reactivity Parameters https://lnkd.in/eh_zn2mw
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FridayFun_Mechanistic Problem_01-03-2024 Try your hand at solving it and see if you can get it right.
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HOW TO REMOVE ALDEHYDE AND REACTIVE KETONE ...... You can use a simple Liquid-Liquid Extraction Protocol to remove aldehyde and reactive ketone residue or contaminants. Add 25 mL of saturated NaHSO3(aq) to a small-scale reaction mixture, shake it for around 30 seconds, then dilute it with 25 mL of H2O. Extract the mixture with 25 mL of 10% EA/hexanes, if the desired product is not too polar.
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SOME REACTION WORK-UP TRICKS Tricky Reaction Solvents: DMF or DMSO (How to remove ????) Very polar and high-boiling solvents that are difficult to remove. If your product is not dangerously polar, dilute it with lots and lots of water before extracting it with a nonpolar solvent. Rule of Thumb: For 5 mL of DMF or DMSO, use 5 X 10 mL of water during the aqueous wash. This should remove all of the DMF or DMSO. Two aqueous washes to remove DMF: 1. 5% LiCl (aq) 2. 0.5 N HCl Boc groups will survive the dilute HCl wash. TMS groups may not. Amine solvents (pyridine, di- and trialkylamines): Amines will partition into the organic layer during a typical aqueous workup. However, they become water-soluble if you 1. Wash the organic layer several times with dilute HCl solution. The protonated amine will be partitioned into the aqueous layer. For use with acid-stable target compounds only. 2. Wash the organic layer several times with 10% copper sulfate (aqueous and blue). The copper-complexed amine will partition into the aqueous solution, which turns purple. Continue to wash with the copper sulfate solution until no colour change is observed. Rule of Thumb: For 5 mL of an amine solvent, use 5 X 10 mL of the 10% aq. CuSO4 solution during the aqueous wash. This should remove all of the amine. Additional pieces of information Aqueous Solutions for Workup Mildly Acidic 1. Ammonium chloride, pH 5-6 (to neutralize) 2. 1N or 2N HCl, pH 1 (to neutralize or acidify) 3. Brine: Removes residual water from the organic layer. The last wash in every workup For Special Purposes: 1. Sodium thiosulfate (10%): to remove bromine or iodine 2.Rochelle's salt (10%): to remove aluminum salts 3. Copper sulfate (saturated): to remove amines 4. Potassium fluoride: to remove trialkyltin byproducts 5. Aqueous ammonium hydroxide/ ammonium chloride (pH 8): to remove copper (I) salts Credit goes to Not Voodoo X.4
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To do science, you need to change your perception
"We don't know what exactly what we will discover because then it would have been discovered already." Watch chemistry laureate Ben Feringa as he tells students how he handles lowlights. You find the full student Q&A here: https://bit.ly/495R6YF
Ben Feringa on lowlights
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