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How do I make Phenol from dichlorobenzene
Most alkyl halides will react with hydroxide to give alcohols through nucleophilic substitution reac ... |
9-1-2014 at 17:34
by: DraconicAcid |
Mysterious gas formation
If you didn't see a precipitate, then you didn't add enough hydroxide to neutralize all the leftover ... |
9-1-2014 at 17:17
by: DraconicAcid |
The Short Questions Thread (4)
That should give you about 12 g of benzoic acid, so getting it hot should dissolve it all nicely. O ... |
9-1-2014 at 13:41
by: DraconicAcid |
The Short Questions Thread (4)
400 mL of water should dissolve about 1.2 g of benzoic acid at RT, and 18 g at 90oC. How much did y ... |
9-1-2014 at 10:35
by: DraconicAcid |
The Short Questions Thread (4)
You should have dissolved it in water, then added the acid to get a precipitate.
If what you have ... |
8-1-2014 at 21:07
by: DraconicAcid |
Aqueus salts, alchohol: I understood it until I didn't
[rquote=314625&tid=28399&author=BromicAcid]It's interesting too that the opposite can happen ... |
8-1-2014 at 16:22
by: DraconicAcid |
Methylamine problem
If I were to attempt a reaction such as this, I would dissolve/suspend the methylammonium chloride i ... |
8-1-2014 at 13:59
by: DraconicAcid |
Aqueus salts, alchohol: I understood it until I didn't
[rquote=314587&tid=28399&author=alexleyenda]By the way, I was experimenting yesterday and ra ... |
8-1-2014 at 13:18
by: DraconicAcid |
Aqueus salts, alchohol: I understood it until I didn't
[rquote=314570&tid=28399&author=jgourlay]
What I don't understand is why the final state of ... |
8-1-2014 at 12:01
by: DraconicAcid |
Methylamine problem
10 kg of methylamine hydrochloride is 148 moles of CH[sub]3[/sub]NH[sub]3[/sub]Cl, and will require ... |
8-1-2014 at 11:58
by: DraconicAcid |
Pronouncing Chemistry Vocab
I-gun-values and book-ner (or byook-ner) filter. |
8-1-2014 at 11:38
by: DraconicAcid |
Aqueus salts, alchohol: I understood it until I didn't
Because the ethanol is much more soluble in water than the salt is- ethanol and water are miscible, ... |
8-1-2014 at 10:15
by: DraconicAcid |
Pronouncing Chemistry Vocab
I used to have a friend who kept saying "tol-you-lane".
Night-rick, Nit-trick...doesn't matter, w ... |
8-1-2014 at 10:11
by: DraconicAcid |
Aqueus salts, alchohol: I understood it until I didn't
The salt is very soluble in water because the dielectric constant of water is very high (it reduced ... |
8-1-2014 at 08:23
by: DraconicAcid |
Pronouncing Chemistry Vocab
In my first year of college, I was taught organic chemistry by a Scotsman who pronounced carbonyl as ... |
7-1-2014 at 10:54
by: DraconicAcid |
The Short Questions Thread (4)
[rquote=314411&tid=25055&author=alexleyenda]When something is soluble in Ethanol, can I assu ... |
7-1-2014 at 10:50
by: DraconicAcid |
Arsenic from Skutterudite
I'm sure its low solubility keeps its toxicity low (although I wouldn't want to leave it sitting on ... |
6-1-2014 at 13:53
by: DraconicAcid |
Thiodinitromethane
As far as I can tell, you're interested in S=C(NO2)2, which should be dinitrothioxomethane. |
6-1-2014 at 13:28
by: DraconicAcid |
Question regarding coordination compounds..
[rquote=314297&tid=28355&author=sankalpmittal]But its a square planar compound. In one book ... |
6-1-2014 at 10:05
by: DraconicAcid |
Crystal solvents
[rquote=314202&tid=28324&author=ScienceSquirrel]They can be labelled in as coordinating liga ... |
5-1-2014 at 18:18
by: DraconicAcid |
Crystal solvents
And the think the thread title should have been "Nonaqueous Solvates"
Come to think of it, the IU ... |
5-1-2014 at 16:53
by: DraconicAcid |
working with gallium aluminium amalgam
I'm not surprised- reaction of isopropanol with metals like sodium and potassium are much less vigor ... |
5-1-2014 at 12:48
by: DraconicAcid |
Crystal solvents
BaSO[sub]4[/sub] is barium sulphate.
Ba(HSO[sub]4[/sub])[sub]2[/sub] is barium hydrogen sulphate, o ... |
5-1-2014 at 12:18
by: DraconicAcid |
Electricity
When I was young, I found the best way to do electrolysis was to use the transformer that came with ... |
4-1-2014 at 20:51
by: DraconicAcid |
Ethyl Isopropyl Ether
You don't want your alkoxide to act as a base; you want it to act as a nucleophile. I would hazard ... |
4-1-2014 at 16:36
by: DraconicAcid |
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