Q: I'm writing a mechanism for the esterification of salicylic acid using thionyl cloride. Then water and diethyl ether. Then sodium bicarbonate.
I remember in lab that when the diethyl ether was added, it was just a washing process. But
A: You need to give more info on what you did. Looking at your sketchy procedure there is stuff missing. What was the objective of the experiment. In any event, the diethyl ether would have been a wash solvent or an extraction solvent; it would not react
Why is diethyl ether is more soluble in water than dihexyl ether? Would you expect propane or diethyl ether to be more soluble in water? Why?
Their ambition was to amalgamate the DHP with benzothiazole atom so that the admixture also had the benign furnishings of benzothiazole. The new action withdrew the use of solvents and alien the use of silica gel and alumina. Secondly, they looked at the abstraction of Stirring to blooming allure, which is an eco-affable, able, and easy-candy allure. They famous that the earlier way to amalgamate compounds included a beef ablution for 2-3 hours and a abatement in booze for up to 15 hours. The problems associated with this accepted adjustment included issues, such as: a conception of abuse, low yields, accessible abrasion due to agitated biological compounds, and also a diffuse and crushing abstracts accumulating action....
Does it react with the molecules? (suppose that the molecules are glucose, p-toluidine, benzoic acid, and 2-naphthol)
Is diethyl ether polar?
What mass ( g ) of the solvent tetrahydrofuran should be combined with 0.6713 L of the solute diethyl ether to produce a solution that is 1.45 m diethyl ether.