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Black Pepper Extraction results!
Too late to edit, but the very end I have 2 quotes. These refer to benzoquinones. |
3-7-2016 at 09:46
by: myristicinaldehyde |
Black Pepper Extraction results!
I have some experience writing papers (humblebrag-  I got 2nd place in the New
York City Quality o ... |
3-7-2016 at 09:43
by: myristicinaldehyde |
Black Pepper Extraction results!
[rquote=453743&tid=66815&author=NEMO-Chemistry][rquote=453334&tid=66815&author=myris ... |
3-7-2016 at 04:51
by: myristicinaldehyde |
Black Pepper Extraction results!
[rquote=453728&tid=66815&author=aga]The OP is YATP so don't hope for too much.
Certainly ... |
3-7-2016 at 04:46
by: myristicinaldehyde |
Butyl acetate -> THF, at all possible/feasible/practical?
See first if you can isolate it from the gel! When extracting painkillers, if a gel formed it's impo ... |
2-7-2016 at 05:35
by: myristicinaldehyde |
Another mechanism question
Very interesting! I wasn't looking to make the indole originally, but it certainly is the path less ... |
2-7-2016 at 05:31
by: myristicinaldehyde |
Another mechanism question
Oh, I'm retarded! No wonder why I failed the test!
It's a ducking ACID BASE REACTION! (The deprot ... |
30-6-2016 at 12:20
by: myristicinaldehyde |
Black Pepper Extraction results!
I will try with white pepper next time- fresh, too. Probably the hydroxide addition and half-assed e ... |
30-6-2016 at 08:13
by: myristicinaldehyde |
Another mechanism question
Interestingly, the Hive's Nicodem says
>>When I said that the deprotonation of o-nitrotoluene ... |
29-6-2016 at 14:53
by: myristicinaldehyde |
Another mechanism question
OK, here are the ones I chose to keep for a "second reading", and some backgrounds
The reaction: ... |
29-6-2016 at 14:31
by: myristicinaldehyde |
Another mechanism question
OK, iminium IS the name, and they do exist. Whether they could play a role is in doubt.
Wiki for t ... |
29-6-2016 at 14:13
by: myristicinaldehyde |
Another mechanism question
The inadequacy was my own- the papers I could read in the entirety were highly technical, and "easie ... |
29-6-2016 at 14:11
by: myristicinaldehyde |
Preparation of Sodium Bisulphite n stuff
Ah, the luxuries of working with concentrated sulphuric acid! I was not trying to kill you. However, ... |
29-6-2016 at 14:03
by: myristicinaldehyde |
Another mechanism question
Chem player posted a very good video a while back about making a precursor to indole (Reissert react ... |
29-6-2016 at 13:42
by: myristicinaldehyde |
Preparation of Sodium Bisulphite n stuff
Aga, when you used copper pipe, a more aggressive way is to use copper powder instead, and then add ... |
29-6-2016 at 13:31
by: myristicinaldehyde |
Black Pepper Extraction results!
So i tried this myself. I used my old, unopened tin of fine black pepper, about 100g (box says 113g, ... |
29-6-2016 at 13:22
by: myristicinaldehyde |
Purifying Copper Sulphate
Tried this myself, but got smaller crystals than I hoped. Next time, cover the beaker! |
29-6-2016 at 13:08
by: myristicinaldehyde |
ethanol recovery
Possibly an ester formed to make triethyl phosphite. Although that seems very unlikely to me.
Or, t ... |
27-6-2016 at 12:59
by: myristicinaldehyde |
Methylation of 1-iodo-2-naphthol
Now, I am no expert, but I always assumed ch3i would make a phenol into a methoxy group. Why wouldn' ... |
26-6-2016 at 06:24
by: myristicinaldehyde |
ChemPlayer the story and the end for now
RIP in spaghetti, never forghetti.
We shall joyously await your Second Coming. |
23-6-2016 at 14:01
by: myristicinaldehyde |
Phosphorus triiodide and DEA List
I don't believe it is watched. It is, however, impossible to ship, just like all the phosphorus hali ... |
20-6-2016 at 16:36
by: myristicinaldehyde |
Raspberry Ketone Synthesis
I found this, which sounds easier (for 4-hydroxybenzyl alcohol)
30 g of phenol are dissolved in ... |
19-6-2016 at 05:05
by: myristicinaldehyde |
Weird reaction, that produces spiky crystals.
Can you filter out the crystals? I am curious to see if they are metal or not, I can't really tell f ... |
18-6-2016 at 12:05
by: myristicinaldehyde |
Weird reaction, that produces spiky crystals.
If it helps, I made a similar Cu-Ni solution (but more Ni), neutralized it with sodium carbonate, an ... |
13-6-2016 at 13:36
by: myristicinaldehyde |
Copper Oxybromide
[rquote=451706&tid=66484&author=Rsambo]If you're at all into colours you should DEFINITELY t ... |
13-6-2016 at 12:35
by: myristicinaldehyde |
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