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Ken asks…
What does diethyl ether do in the esterification of salicylic acid?
I'm creating a mechanism for the esterification of salicylic acid utilizing thionyl cloride. Then drinking water and diethyl ether. Then sodium bicarbonate.
I don't forget in lab that when the diethyl ether was extra, it was just a washing procedure. But I don't realize how it would in shape into a mechanism.
Did it have a objective? what did it chemically do to the molecule?
ItIsAllHere solutions:
You want to give more data on what you did. Hunting at your sketchy process there is things missing. What was the goal of the experiment. In any celebration, the diethyl ether would have been a wash solvent or an extraction solvent it would not react underneath these conditions.
Susan asks…
Why is diethyl ether is more soluble in water than dihexyl ether?
Why is diethyl ether is much more soluble in water than dihexyl ether? Would you anticipate propane or diethyl ether to be much more soluble in drinking water? Why?
ItIsAllHere solutions:
That is since hexyl group is much more NON-Roman policier and bulky than ethyl group.. Providing much a lot more repulsion to polar water molecule...
Hope I aid you with that .. Goodluck and godbless!
Richard asks…
Why are molecules much more soluble in diethyl ether than in water?
Does it react with the molecules? (suppose that the molecules are glucose, p-toluidine, benzoic acid, and two-naphthol)
Is diethyl ether polar?
ItIsAllHere solutions:
There is a easy rule that is effortless to remember and stick to..."like dissolves like". What it implies is that solvents which have selected physical traits will dissolve solutes that have related bodily qualities. At it is most general which means, orgainc solvents will dissolve organic and natural compounds. That being stated, all the compounds you outlined will dissolve in diethyl ether. Even so, not all of the compounds you detailed are Much more soluble in diethyl ether than h2o. Glucose, for one particular, is in fact a lot more soluble in drinking water than it is in ether. The cause is since water is far more polar than ether and can hydrogen bond with h2o a lot more freely than with ether because h2o has each hydrogen bond donor and acceptor atoms. Similarly, the more 'hydrocarbon-like' a solute is (with two-napthol getting the most hydrocarbon-like compound of the types detailed), the far more soluble it will be in a lot less polar solvents.
Hope this helps!!!
Maria asks…
What mass ( g ) of the solvent tetrahydrofuran need to be merged with .6713 L of the solute diethyl ether to?
What mass ( g ) of the solvent tetrahydrofuran need to be blended with .6713 L of the solute diethyl ether to create a answer that is 1.forty five m diethyl ether.
ItIsAllHere solutions:
_____molality is moles of solute / kg solvent
right here THF is the solvent and Et2) is the solute
moles solute = 671.3 ml * d Et2O g/ml / MW Et2O g/mole = ?? Moles Et2O
one.45m = one.45 moles / kg = ?? Mole / x kg of solvent
x g of solvent = a thousand g/kg * ?? Mole Et2O /one.forty five mole/kg = ?? G THF
Plug missing data and Clear up
Standard mathematics is a prerequisite to chemistry – I just attempt to assist you with the methodology of fixing the problem.
John asks…
What are the effects of Diethyl ether on you?
Can anybody inform me the outcomes of Diethyl Ether when you sniff it?
ItIsAllHere solutions:
Diethyl ether is a colourless, very unstable liquid with a attribute smell. It is employed as am anaesthetic, although it is not an best anaesthetic. It is safer than chloroform and more efficient than nitrous oxide. Unwelcome consequences of coverage to ether can consist of a cough, sore throat, painful red eyes, a headache, drowsiness, laboured respiration and nausea. Vomiting is very frequent.
But some folks like its sub-anaesthetic effects on consciousness when you sniff it it has "abuse possible".
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