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Electrochemistry - (maybe) stupid question
Can we make a reaction go by building correct galvanic cell?
For example: iodine and oxalic acid do ... |
8-10-2018 at 03:31
by: MKSStal |
What to use Na2S2O3 for?
I will get about 3 kg of sodium thiosulfate. Any ideas for some cool use of it? Maybe some special m ... |
31-7-2018 at 14:25
by: MKSStal |
SN2 with chloroform anion
Why is it so? Due to chloroform anion decomposition to dichlorocarbene, and further hydrolysis?
In ... |
19-7-2018 at 12:18
by: MKSStal |
SN2 with chloroform anion
Do you think, that SN2 can be performed using some alkyl halide, chloroform and hydroxide to deproto ... |
19-7-2018 at 11:06
by: MKSStal |
Methyl acetate and acetone separation
Do you think that standing over sodium bisulfite even for long time with some shaking might do the w ... |
27-12-2016 at 11:03
by: MKSStal |
Methyl acetate and acetone separation
I have a solvent containing both methyl acetate and acetone. They have very similar boiling points a ... |
26-12-2016 at 02:41
by: MKSStal |
57% Hydriodic Acid Solution
I've read a suggestion to put some copper in HJ solution after preparing it. So, I've got a question ... |
25-8-2016 at 14:32
by: MKSStal |
Potassium chlorate waste
The one, I'm going to do? So, I had an opportunity to buy barium chlorate. I would react it with pot ... |
25-8-2016 at 02:05
by: MKSStal |
Potassium chlorate waste
Nothing, but 150g is far too much and I would like to perform some synthesis. KClO3 itself is quite ... |
25-8-2016 at 01:46
by: MKSStal |
Potassium chlorate waste
As a second product of reaction, I'm planning to do, I will get about 150g of potassium chlorate. An ... |
25-8-2016 at 00:52
by: MKSStal |
Sulfonamide hydrolysis
I want to ask if it is possible or hard to hydrolyse sulfonamides? Because for me reactions of NaOH ... |
29-11-2015 at 03:34
by: MKSStal |
Bromine from bromoform
So, I already bought 250 ml of pure (according to etiquette) bromoform for 22 złote (PLN) = 5,65 US ... |
5-11-2015 at 14:33
by: MKSStal |
Quaternary ammonium salt from triethanolamine
So, I tried to test it. On Tuesday I mixed about 13,2 ml (0,1 mol) of triethanolamine with 11,5 ml ( ... |
30-10-2015 at 09:14
by: MKSStal |
Quaternary ammonium salt from triethanolamine
Caro acid won't also oxidise hydroxyl groups to aldehydes or rather carboxilic acids? |
25-10-2015 at 01:51
by: MKSStal |
Quaternary ammonium salt from triethanolamine
So in my opinion it depends on which alkyl halide would be used. For 1' reaction with alcohol should ... |
25-10-2015 at 00:16
by: MKSStal |
Quaternary ammonium salt from triethanolamine
For me typically used triethylamine is barely accesible. So I thought about reacting triethanolamine ... |
22-10-2015 at 09:54
by: MKSStal |
Bromine from bromoform
Ok, now I know, that benzene couldn't be used, because it's Reimer-Tiemann reaction and it needs phe ... |
24-5-2015 at 05:03
by: MKSStal |
Stuff in my Disulphur Dichloride
Tops of that bottles probably tend to discolour. In my example I have blue top with huge white circl ... |
24-5-2015 at 04:30
by: MKSStal |
Bromine from bromoform
I think it's all about this specific shop. They have very unreasonable prices in few cases. For exam ... |
24-5-2015 at 01:49
by: MKSStal |
Bromine from bromoform
I have seen a shop in which I can buy pure bromoform in quite a good price. Calculating per mole of ... |
23-5-2015 at 10:33
by: MKSStal |
Copper acetate and acetone?
Adding acetone or some similar organic solvent is a popular way to participate some ionic, water sol ... |
4-5-2015 at 09:52
by: MKSStal |
