Ken asks…
What does diethyl ether do in the esterification of salicylic acid?
I'm writing a mechanism for the esterification of salicylic acid employing thionyl cloride. Then h2o and diethyl ether. Then sodium bicarbonate.
I keep in mind in lab that when the diethyl ether was extra, it was just a washing procedure. But I will not recognize how it would in shape into a mechanism.
Did it have a purpose? what did it chemically do to the molecule?
ItIsAllHere solutions:
You need to give a lot more data on what you did. Seeking at your sketchy method there is things lacking. What was the objective 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 drinking water than dihexyl ether?
Why is diethyl ether is far more soluble in h2o than dihexyl ether? Would you expect propane or diethyl ether to be much more soluble in drinking water? Why?
ItIsAllHere solutions:
That is simply because hexyl group is much more NON-Roman policier and cumbersome than ethyl group.. Giving much much more repulsion to polar water molecule...
Hope I help you with that .. Goodluck and godbless!
Richard asks…
Why are molecules 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 2-naphthol)
Is diethyl ether polar?
ItIsAllHere solutions:
There is a basic rule that is easy to don't forget and stick to..."like dissolves like". What it signifies is that solvents which possess certain bodily characteristics will dissolve solutes that have comparable bodily qualities. At it really is most common meaning, orgainc solvents will dissolve organic and natural compounds. That staying explained, all the compounds you outlined will dissolve in diethyl ether. Nonetheless, not all of the compounds you listed are More soluble in diethyl ether than water. Glucose, for one particular, is actually a lot more soluble in drinking water than it is in ether. The reason is simply because water is more roman policier than ether and can hydrogen bond with drinking water far more freely than with ether given that h2o has equally hydrogen bond donor and acceptor atoms. Equally, the far more 'hydrocarbon-like' a solute is (with 2-napthol staying the most hydrocarbon-like compound of the kinds outlined), the far more soluble it will be in less polar solvents.
Hope this will help!!!
Maria asks…
What mass ( g ) of the solvent tetrahydrofuran should be merged with .6713 L of the solute diethyl ether to?
What mass ( g ) of the solvent tetrahydrofuran should be combined with .6713 L of the solute diethyl ether to make a solution that is one.forty five m diethyl ether.
ItIsAllHere answers:
_____molality is moles of solute / kg solvent
right here THF is the solvent and Et2) is the solute
moles solute = 671.three ml * d Et2O g/ml / MW Et2O g/mole = ?? Moles Et2O
1.45m = one.forty five moles / kg = ?? Mole / x kg of solvent
x g of solvent = one thousand g/kg * ?? Mole Et2O /1.45 mole/kg = ?? G THF
Plug lacking info and Remedy
Simple mathematics is a prerequisite to chemistry – I just consider to help you with the methodology of fixing the dilemma.
John asks…
What are the consequences of Diethyl ether on you?
Can anybody notify me the effects of Diethyl Ether when you sniff it?
ItIsAllHere solutions:
Diethyl ether is a colourless, extremely volatile liquid with a characteristic odor. It is utilized as am anaesthetic, despite the fact that it is not an best anaesthetic. It is safer than chloroform and far more successful than nitrous oxide. Unwelcome results of exposure to ether can include a cough, sore throat, distressing red eyes, a headache, drowsiness, laboured respiration and nausea. Vomiting is quite widespread.
But some people like its sub-anaesthetic results on consciousness when you sniff it it has "abuse potential".
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