Why is ethanol (vs. water) commonly used as a solvent during chloro(pyridine)cobaloxime(III) synthesis?
Chloro(pyridine)cobaloxime(III) is also named as Chloro bis ( dimethylglyoximato) ( pyridine) cobalt (III).It is widely used as a catalyst for C-C ,C-O , C-N, C-H bond formation.when ethanol vs water (aqueous ethanol) is used as a solvent for the preparation , this cobaloxime compound has less solubility in this organic solvent such as ethanol.due to their low solubility chloro pyridine cobaloxime (III) and cobaloxime (II) can be easily removed by adsorptive filtration of the reaction mixture in a short silica gel coloum.
Why is ethanol (vs. water) commonly used as a solvent during chloro(pyridine)cobaloxime(III) synthesis?
Why can 95% ethanol be used as a solvent in the synthesis of 2-butoxynaphthalene? I thought that for an Sn2 mechanism only aprotic solvents can be used for the synthesis?
What is the solvent used in the Sn1 reaction between water and 2-chloro-2-methylpropane... in our experiment we used 2-chloro-2-methylpropane in acetone and NaOH. Would the solvent just be acetone and water? and NaOH acts as the nucleophile?
the solvent available are water, water mixed with ethanol,
ethanol, and toluene.
as for the unknown compounds we had:
methyl-p-nitrobenzoate
acetanilide
benzoic acid
phenacetin
acetylsalicylic acid
salicylic acid
acetaminophen
4-aminiobenzoic acid
Question 4: Look at the 4 solvents that you tested and the possible structure of the unknowns. Is there one solvent that you think might dissolve all these compounds at room temperature? Which one and why does it make sense in terms of IMF. (Hint: "like dissolves like "+...
Briefly explain why ethanol, and not hexane, is used as a solvent in the Suzuki-Miyaura coupling reaction.
Why is phthalic acid better recrystallized in water solvent rather than using ethanol or diethyl ether as solvent for the phthalic acid?
Draw a mechanism for a green aldol synthesis without solvent. using 3,4-dimethoxybenzaldehyde, 1-indanone, NaOH, HCl, ethanol and water
1. Predict the products of the following reactions (18 points, 3 each) Catalytic KOH methanol/water solvent Catalytic KOH methanol/water solvent Catalytic KOH methanol water solvent Catalye KOH. 1 equivalent NaOCH.CH ethanol solvent I equivalent NaOCH.CH ethanol solvent 2. Write the product of the following reaction and the full mechanism by which it is formed. Clearly show which steps are reversible and which one step is irreversible. (8 points). 1 equivalent NaOCH CH3 cthanol solvent + excess 3. Circle the most...
why would HCl be an inappropriate solvent to elute Cr(III) complexes from a column during ion exchange chromatography?
Acetone, whose structure is shown below, is a laboratory solvent that is also commonly used as a nail polish remover. What is the strongest intermolecular force in a sample of pure acetone? What is the strongest intermolecular force that occurs between acetone and water?
Why is EtOH not ideal for the Williamson ether synthesis? What would be a better solvent choice? Why isn't the better solvent choice used on a large industrial scale? Consider the cost and waste disposal.