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We're recovering from a major server loss and are restoring backups as we gain access to them. Don't mind the odd time warp. Warn us in the future.

Your recommended method of extracting DMT? by Matilda Hittingtut - Sat, 18 Aug 2018 10:13:51 EST ID:Udk0Y39+ No.79204 Ignore Report Reply Quick Reply
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I was looking up how to extract DMT and apparently it's most commonly done with Mimosa Hostilis root bark. Looking at the guides it's very MacGyver tier. I'm saying I'm wondering if there is a more professional way of doing it. Essentially I'm asking, if you ever looked into extracting DMT and if you have the chemistry background, what methods of extraction do you prefer/recommend and do you have any advice regarding it? Perhaps a mistake that commonly diminishes the quality of the extraction or some deviation from the existing guides to end up with something more pure.
trypto - Sat, 18 Aug 2018 15:30:50 EST ID:OdR7meD+ No.79205 Ignore Report Quick Reply
Rotovaps make chemistry much, much, much easier. That's a device that evaporates solvents very quickly.

Solvent choice is also very helpful. The amateur has to choose between a few commonly available solvents meant for shit like paint-stripping. Professionals can choose a solvent that has analytical standards, and is harder to obtain (can't get at the hardware store).

Pros also have better filtration systems. This is less expensive than the rotovap, and not as much as a time save, but still very helpful.

TLC plates help keep track of whether or not product is there (so you can be more efficient when pulling).

Better ventilation is nice.

Lab freezers are better than home freezers, and usually have safeguards to prevent blowing up.

In the end, if you have white crystals, it's a reasonably pure product. Crystallization is cool like that. However, a well-stocked lab will get higher yields in less time.
Edward Digglepadge - Thu, 11 Oct 2018 22:40:06 EST ID:Ub0k3Gmq No.79242 Ignore Report Quick Reply
When doing TLC I am separating by molecular weight, no? If so, how do I predict how many bands I should get during these sorts of processes?
Sry if these are silly questions. I am a physicist only familiar with a bit of chem, mostly spectroscopy.
puress - Fri, 12 Oct 2018 13:48:21 EST ID:bibGzGaZ No.79243 Ignore Report Quick Reply
TLC is most often distribution chromatography ( with a smidgeon of absorption chromatography) , meaning its more about polarity of the substances than about their weight itself (though there often is an indirect relation between weight to affinity). you basically have a solvation hull on your substrate and the mobile phase flows above that, depending on the polarity of a substance it moves between the stationary and the mobile phase, thus seperating from other substances. ive made a nice animation for that shit but im too paranoid, ill see if i find a comparable animation

in theory you should get one band per compound of your mixture but high concentrations or an unsuitable eluent may lead to streaking and improper seperation depending on the number of theoretical seperation stages.

in the OP scenario TLC would only serve as an analytic tool, even column chromatography couldnt really yield a lot of DMT doses

youd be seperating by molecular weight if the different compounds had no intrinsic dipoles. i used to hate chromatography since its such a bitch ass compromising bullshit way of seperation... wait theyre all based on equilibrium
purrbastus - Sat, 20 Oct 2018 04:31:22 EST ID:L5efXmCV No.79256 Ignore Report Quick Reply
you can do TLC on a large enough plate after plating it on glass and then chisel the silica or alumina off it to extract it back out

you can do that up to like 2g of a sample depending how many silica coats you do and how patient you are. works for analytic and organic chemistry. definitely not for others. but then again, if you're operating with fucking oxymorphone or dmt or cocaine for personal usage, this may be viable.
pupress - Thu, 25 Oct 2018 16:21:28 EST ID:KFcL1XHa No.79269 Ignore Report Quick Reply
put my gold fish into the bath tub so that the aquarium is free to serve as a tlc chamber

bright star tek questions by Ernest Duckson - Thu, 13 Sep 2018 13:45:15 EST ID:HJwBSxjU No.79229 Ignore Report Reply Quick Reply
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One is left with impure methylamine. The stuff includes ammonia chloride.
Is this fine? Is one to assume that when using the adulterated methylamine in later reaction that the ammonia chloride wont matter?

Step 3 says to "flood the reaction contents with 1.5 L of slightly acidic water"
Mix in what container? Largest container called for is 1000ml RBF
Clara Chugglespear - Mon, 22 Oct 2018 19:59:29 EST ID:g2RTfgmx No.79264 Ignore Report Quick Reply

Or i could just buy mdma off the derp web

Reducing 3,4,5-trimethoxy-beta-nitrostryrene to mescaline by Matilda Bomblehit - Wed, 13 Jun 2018 11:03:55 EST ID:rajg/xs8 No.79145 Ignore Report Reply Quick Reply
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I want to reduce 3,4,5-trimethoxy-beta-nitrostyrene to the amine. What will do this? I've found so much worthless and bullshit information. It seems the main options are:

  1. Zn/HCl or Fe/HCl. I don't know if this goes from the nitrostyrene to the amine or if I need to use NaBH4 to first reduce the double bond. Also, some people say the yields are good and others say the yields are shit.

2. LAH. Not an option.

3. SnCl2 to reduce the nitrostyrene to an oxime and then Zn to reduce the oxime to the amine. I've never found proof of anyone doing this reaction on nitrostyrenes. SnCl2 is good for reducing nitropropenes but who knows if that applies to nitrostyrenes.

4. Al/Hg. Literally toxic. I haven't found any reports of people using the less toxic Al/Ga or Al/Cu amalgam. I also get conflicting information saying Al/Hg reduces directly to the amine, yet others are saying NaBH4 must be used to first reduce the double bond and then the Al/Hg reaction can be run to reduce the nitro group to an amine -- which is it?

Any input would be appreciated, especially from people who have actually run these reactions on this particular substrate.
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Phoebe Wicklefoot - Wed, 20 Jun 2018 13:34:12 EST ID:f7Wsgp11 No.79148 Ignore Report Quick Reply
Are you planning on making larger quantities? if not, just go with al/hg. use your common sense and everything will be fine. solubility of mercury salts in organic solvents is negligible. when you worry about the organomercury compounds, just give your product (salt) a proper wash with organic solvents and acetone and you are golden
Archie Duckstone - Tue, 21 Aug 2018 22:59:51 EST ID:zbIVdkqy No.79213 Ignore Report Quick Reply
fucking crush it with hot hydrogen
Samuel Turveydock - Wed, 22 Aug 2018 20:39:00 EST ID:zbIVdkqy No.79215 Ignore Report Quick Reply
pushing it through a pad of celite or silica would help but honestly there isnt any reason to go with mg or tin
ochem portal has a page dedicated to conjugated nitro reductions...
Martin Drablingville - Thu, 23 Aug 2018 15:55:31 EST ID:quGHpYNb No.79217 Ignore Report Quick Reply
Zn/HCl is the method of choice for terminal nitrostyrenes, but it fails for nitropropenes. Fe/HCl gives carbonyl compounds which you don't want. Make sure your zinc is good.
Bombastus Werrywag - Sat, 20 Oct 2018 04:35:52 EST ID:L5efXmCV No.79258 Ignore Report Quick Reply
double bond may prevent the latter but either sources of hydrogen should work. then introduce it with palladium on carbon under a little party balloon to give you the pressure required to hydrogenate that 2nd position

Naltrexone -> Oxymorphone? by Hamilton Beggleshit - Thu, 17 Mar 2016 18:16:02 EST ID:GksK9UMc No.77752 Ignore Report Reply Quick Reply
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Dear /chem/,

wikipedia cites that "Naltrexone can be described as a substituted oxymorphone – here the tertiary amine methyl-substituent is replaced with methylcyclopropane. Naltrexone is the N-cyclopropylmethyl derivative of oxymorphone."

Is it possible to revert naltrexone back to oxymorphone? If so, how?

My very limited understanding of organic chemistry leads me to believe that naltrexone could, in proper solution and (probably) with the addition of heat, be broken into oxymorphone and cyclopropylmethylbromide. (pic related)

Any input regarding said (hypothetical) reaction will be greatly appreciated!
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Molly Nadgedale - Sun, 01 Jul 2018 20:46:17 EST ID:OdR7meD+ No.79157 Ignore Report Quick Reply
Google is your friend. Show the minimum effort at least.
Piemaster - Fri, 06 Jul 2018 05:57:39 EST ID:pv6fN59z No.79162 Ignore Report Quick Reply
Would it be possible to turn the cyclopropane into a terminal alkene using aluminum or something? I know cyclopropane's are very unstable.

And then would it possible to attach a carbon to the terminal alkene? You could attach a phenyl or something and make n-phenylpropyl.

Basically to sum up what I'm saying, instead of trying to remove the cyclopropylmethyl group outright, would it be possible to turn it into a 4 carbon chain, the last C=C being a double bond? And then using the reactivity of said double bond to attach something? You'd be able to make a pretty potent agonist that way.
Alice Honeyhall - Mon, 09 Jul 2018 03:51:31 EST ID:mH/x48p3 No.79163 Ignore Report Quick Reply
Cyclopropanes are very unstable but the one pictured with a stabilized alkane group is not. This group shown with an R-cyclopropane is relatively stable.
Carbon-carbon chemistry is very hard. Even harder to do selectively.

Short answer is most likely, no.
Edwin Clarryforth - Tue, 18 Sep 2018 23:44:00 EST ID:y5OCfqyd No.79231 Ignore Report Quick Reply

The cyclopropylmethyl can be turned into isobutyl via palladium under hydrogen. How hard would it be to remove it then?
Pressbastus - Sat, 20 Oct 2018 04:33:55 EST ID:L5efXmCV No.79257 Ignore Report Quick Reply
oh yeah how have we been going with this? OP did you make any significant literature readings or apply common reactions to make this even remotely practical?

ATTENTION SMART PEOPLE by Archie Sackleware - Thu, 18 Oct 2018 16:19:01 EST ID:+P3OcrX6 No.79249 Ignore Report Reply Quick Reply
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I'm dumb as a brick and just want to make sure that I'm getting this right. Is the information in this link saying that L-Carnitine has a pH of 6.5 to 8 when mixed in a solution of 50 grams L-Carnitine to 1 liter of water?
1 posts omitted. Click Reply to view.
Esther Pattingson - Thu, 18 Oct 2018 21:21:00 EST ID:WFjboSki No.79251 Ignore Report Quick Reply
Well shit, thanks. I don't suppose you know the pH of L-Carnitine by chance?
Wesley Muttingridge - Thu, 18 Oct 2018 23:13:57 EST ID:dl9lAnzN No.79252 Ignore Report Quick Reply
Well, from what I can tell, Carnitine in its ground racemic state isn't ionic or a proton donor (but someone who knows for sure should correct me if that's wrong)-- which means it doesn't have a pH at all. pH is a measure of the electrical properties of water, so anything that isn't water nor has a free ion nor is a proton donor doesn't participate in the pH system (directly, again, since they might catalyze something else that does effect pH, particularly in a living organism.)
Thomas Honeyspear - Fri, 19 Oct 2018 09:57:48 EST ID:WaGAkLIJ No.79253 Ignore Report Quick Reply
So if you had to make a guess would you assume that pure L-Carnitine crystals would be safe for teeth when dissolved in water? I need to take 3.5g a day and I worry about it's affect on my teeth, especially since I have a chipped tooth that I can't afford to get capped.
Wesley Muttingridge - Fri, 19 Oct 2018 17:59:04 EST ID:dl9lAnzN No.79254 Ignore Report Quick Reply
Yeah man, should be fine. If you're really concerned about it, drink it with a straw past your teeth straight down your throat, but honestly I think you should be fine.
Eugene Pennersock - Fri, 19 Oct 2018 18:40:40 EST ID:QAuHu/mb No.79255 Ignore Report Quick Reply
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Excellent. Thanks man, here's a picture of Jenna Fischer for your assistance.

Organic chemistry by Reuben Hurringnat - Tue, 16 Jan 2018 12:06:23 EST ID:uUZ+g3Ph No.78973 Ignore Report Reply Quick Reply
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What's the best way to learn organic synthesis outside of picking up a text book?
Any online courses or videos out there?
Rebecca Trotville - Mon, 21 May 2018 20:12:41 EST ID:gvFzbxwU No.79108 Ignore Report Quick Reply
Khan academy
Katsuragi !/pe1aKvMmQ - Thu, 24 May 2018 22:02:34 EST ID:4Q6JexVr No.79127 Ignore Report Quick Reply
Rebecca Dranningbane - Tue, 16 Oct 2018 23:43:26 EST ID:wRB//qcg No.79247 Ignore Report Quick Reply
Alice Packlelone - Wed, 17 Oct 2018 14:36:56 EST ID:3wTRifUB No.79248 Ignore Report Quick Reply
How is that link relevant?

4fmph by Caroline Hunningsat - Thu, 20 Sep 2018 17:02:33 EST ID:JsuSKLxG No.79232 Ignore Report Reply Quick Reply
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Can I turn all this 4F-MPH, this 4fluoro-methylphenidate, into plain old methylphenidate (Ritalin) ? For studying? Assume ive dabbled extensively in kitchen chemistry (assume I'm not as feeble in the lab as I am in the psychiatrist offices)
i know its a long shot and im pretty much asking for my work to be done for me but what the hell. the man is on a mission to go back to school
puress - Mon, 24 Sep 2018 03:15:57 EST ID:EOf7gf9L No.79235 Ignore Report Quick Reply
nope, wont work
Lillian Cogglehack - Thu, 27 Sep 2018 19:46:25 EST ID:xsneeAgl No.79236 Ignore Report Quick Reply
Op here

Im willing to be a good chemist with unlimited resources could do it....
Name - Thu, 27 Sep 2018 19:47:34 EST ID:xsneeAgl No.79237 Ignore Report Quick Reply
William Brinkinwick - Thu, 27 Sep 2018 22:42:23 EST ID:oKyR6MUr No.79238 Ignore Report Quick Reply
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Fluorine is the most electronegative element. It grabs on to shit and doesn't let go. It's almost certainly possible to do what you're asking, but not necessarily in a one step reaction, and certainly not easily

Science denialist vent/ rant. by James Mother Fucking Randi - Fri, 31 Jul 2015 04:30:23 EST ID:FW3hqiSI No.76865 Ignore Report Reply Quick Reply
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I started a thread on /spooky/ asking for any evidence of the paranormal or supernatural.

Instead all I got was a bunch of personal attack and people babbling nonsense and presenting it as truth. Then when shown they are incorrect with verifiable data rather than pseudoscience they resort to personal attacks again. They and pretty much all other magical thinkers take any sort of challenge to their beliefs as a personal attack.

I was at a party a few months back and some girl was talking about how she went to some yoga guy who does "laying on of hands". Which involves doing yoga while a dude puts his hands on your body and makes weird noises. Supposedly doing this achieves any number of effects from healing wounds, curing depression and other supposed boons.
not arguing the therapeutic effects of yoga just the laying on of hands part
I tried to understand what she was explaining to me by asking questions. Like asking her what was actually happening because it made 0 sense to me. Instead she started insulting me for being closed minded and shit.

Also in real life I live in the US south. Where people who think the world is 6000 years old is the norm.

Needless to say I deal with people who use magical thinking on a regular basis.
They are 100% willing to reap the benefits of science and the technology that comes with it until it conflicts with some myth or story about ghosts or some shit some one told them. Then all reason and logic go out the window.

Why do so many people especially in the us reject verifiable facts over what feels good? I went to the same public schools as them, I was also raised in a religious household (jewish, although I'm no longer religious). The only difference is that I chose the rational answer.
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Samuel Pittway - Mon, 12 Oct 2015 15:06:58 EST ID:/dGkbVvd No.77281 Ignore Report Quick Reply
Since we all know that nothing can be 100% proven, I think the word "proof" can imply an implicit acknowledgement of that fact.
Reuben Sanderfoot - Tue, 13 Oct 2015 01:26:14 EST ID:uGD5aNS6 No.77282 Ignore Report Quick Reply
Its more appropriate to just say "indicates" or "we hypothesize".

I agree, I just tend to shy away from the word. What happens all the time is the scientific community accepts something in a consensus, only to have that consensus overturned or it falls to more complete models. As you said, just try to keep a healthy dose of skepticism of everything since we are so far away from total understanding of anything, especially in the realm of physiology.
Samuel Nishson - Thu, 29 Oct 2015 03:51:53 EST ID:A6yjNMdA No.77338 Ignore Report Quick Reply
>I was at a party a few months back and some girl was talking about how she went to some yoga guy who does "laying on of hands". Which involves doing yoga while a dude puts his hands on your body and makes weird noises. Supposedly doing this achieves any number of effects from healing wounds, curing depression and other supposed boons.

She was probably just saying that because she wanted you to be sceptical and then invite her to demonstrate or whatever out of "curiosity" and it would all quickly escalate into sex.

I won't believe a girl could genuinely be that ditzy.
Cornelius Sublingham - Fri, 21 Sep 2018 11:43:24 EST ID:H2dReURr No.79233 Ignore Report Quick Reply
>>76949 bump for spooky
Rebecca Fangold - Sat, 22 Sep 2018 16:38:11 EST ID:dl9lAnzN No.79234 Ignore Report Quick Reply
>>Its more appropriate to just say "indicates" or "we hypothesize".
Didn't read the thread so don't know if anyone has already mentioned this, but you should look into something called 'English Prime.'

Basically it takes the concept of the Sapir-Whorf hypothesis (that language creates mental state, that ideas possible to be expressed within a language are the borders of the space in which speakers of that language can have ideas at all) and uses it to attempt to fix English by making it more explicitly scientific.

For example, it removes almost all constructions of 'to be' including 'is' and 'are.' Nothing is good, or bad, or blue, or fast, but can seem, or appear, or correlate to those properties. It basically forces people to remove the unscientific and unprovable but completely common habit of claiming things 'are' things, reducing it to the simple truth; that they seem to be things, and deliberately denying the power to speculate beyond to 'the thing in itself.'

OTC Nonpolar Solvent by Graham Bunfoot - Thu, 07 Jun 2018 01:15:44 EST ID:3wTRifUB No.79140 Ignore Report Reply Quick Reply
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What's something pure and reliable I can use a nonpolar solvent that I can quickly buy?
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Bombastus Werrywag - Sun, 10 Jun 2018 22:51:45 EST ID:iycOEdHd No.79143 Ignore Report Quick Reply
what's wrong with gasoline?
press - Mon, 11 Jun 2018 12:50:16 EST ID:MfoZ/ogu No.79144 Ignore Report Quick Reply
dont you north americans have colemans fuel or naptha or something like that? something more like petroleum ether than gasoline.

what kind of compound do you want to extract? perhaps xylene or toluene would be better and almost as easy to source.

nail polish remover is mostly ethyl ethanoate nowadays aint it, well atleast the faggy shit thats aetone free. real man remove their nail polish with acetone containing nail polish remover.
Archie Duckstone - Tue, 21 Aug 2018 23:01:05 EST ID:zbIVdkqy No.79214 Ignore Report Quick Reply
why do you want freebase?
Martin Drablingville - Thu, 23 Aug 2018 15:57:14 EST ID:quGHpYNb No.79218 Ignore Report Quick Reply
I don't know what the fuck you can buy but the standard answers are "acetone", "methyl ethyl ketone", "dichloromethane", "toluene" and "petroleum ether", in decreasing order of polarity. Some distillation may be required.
Martin Drablingville - Thu, 23 Aug 2018 15:58:06 EST ID:quGHpYNb No.79219 Ignore Report Quick Reply
based on your other reply, DCM is the best choice here, or MEK or toluene. pet ether is too weakly solvating and acetone is too polar.

What makes atoms do what they do? by Matilda Hassleway - Sat, 10 Mar 2018 11:49:56 EST ID:PTghO7Nx No.79012 Ignore Report Reply Quick Reply
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Sup /chem/,

There is a fundamental gap in my understanding of the universe. When we look out into the sky and see the sun and stars, measure the Earth orbiting the sun, or see a volcano, it is commonly accepted that eventually, all of these processes will run out of energy and cease to do their thing. However every atom in the universe has positive and negative charges, with the negatively charged particles constantly in motion (and i guess the positive ones too if we count vibration or whatever). How do subatomic particles get a charge in the first place? Will it ever wear off? What makes electrons move? Will an electron ever stop moving and become neutrally charged? Can we apply this seemingly infinite source of subatomic energy to the macro scale to prevent a big freeze or one day generate limitless energy?
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trypto - Sun, 19 Aug 2018 12:24:48 EST ID:OdR7meD+ No.79208 Ignore Report Quick Reply
>why did the universe develop with electrons and protons instead of positrons and positrons?
Should be antiprotons and positrons. Good lord there's a lot of weird typos in that post.
trypto - Sun, 19 Aug 2018 13:06:02 EST ID:OdR7meD+ No.79209 Ignore Report Quick Reply
OK. I'll finally try to follow up. Quickly.

In the last post, I brought us up to the point where physicists saw that light is emitted in packets called 'quanta' at the time. They knew that because of theoretical work following the 'ultraviolet catastrophe'.

But they also knew light acts as a wave, since a single wavelength passing through two slits produces a diffraction pattern (like water waves going through small slits). This is Young's double slit experiement, and was actually an early 19th century experiment (predating most of the experiments I'm talking about here).

They also knew light is a wave because Maxwell's Equations can be used to describe light as an electromagnetic wave very accurately.

But, unlike waves, light didn't appear to travel through any medium. Sound travels through air, ocean waves through water, 'guitar waves' on taught strings, etc. They called the theoretical media that light uses "ether", but attempts to prove its existence failed (the michelson morley experiement).

They also realized that, in many cases, light spectra weren't smooth and continuous. They had very sharp, unexpected lines.

Also at this time, Einstein described the photoelectric effect, where light could be absorbed in quanta
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trypto - Sun, 19 Aug 2018 13:29:31 EST ID:OdR7meD+ No.79210 Ignore Report Quick Reply
To recap: At this point, the long-held theory that light is a wave was being challenged by a bunch of experiments/models.

And then, while trying to figure that shit out, a bunch of experiments/models suddenly showed that MATTER is a wave.

This is still really only the preamble to quantum mechanics, and it's where the math starts to get more intense. Until this point, the math involved was pretty much calculus and differential equations

The next big experiment would be the one that hippies and armchair philosophers love, which is the variation of the double-slit experiment where observation changes the expected outcome. People try to extrapolate so much metaphysical bullshit with this experiment, and I hate it. Yes, it's an amazing result. yes, the math is deep and profoundly alters how we view reality or truth itself. But at the same time, it's simply a mathematical model that's describing what we see. And then we call it reality. It's boring.

IF I do another post, I'll try to explain this experiment, the math it spawned, and the (legit) philisophical interpretations. This is where linear algebra comes into play, infinite arrays, the schrodinger equation, imaginary numbers, wave equations, and more. IMO, it's the point where "quantum weirdness" becomes solved for the most part. There's some philisophical differences of opinion, but they're not too important.
trypto - Sun, 19 Aug 2018 13:35:45 EST ID:OdR7meD+ No.79211 Ignore Report Quick Reply
>A positive charge interacts with a positive charge differently than a negative charge interacts with a negative charge.
Also, fuck. This should be "A positive charge interacts with a positive charge diferferently than a POSTIVE charge interacts with a negative charge".

Of course, P-P interactions are identical to N-N interactions.
trypto - Sun, 19 Aug 2018 13:48:46 EST ID:OdR7meD+ No.79212 Ignore Report Quick Reply
> IMO, it's the point where "quantum weirdness" becomes solved for the most part. There's some philisophical differences of opinion, but they're not too important.
Oh yeah, and of course special relativity/gravity is still an open question in regards to quantum-scale. Blefht. I'm done. These rambling posts brought to you by Bush. Breakfast of champions.

Fuckin Minerals by Lydia Bingernudging - Tue, 07 Aug 2018 01:29:22 EST ID:dl9lAnzN No.79190 Ignore Report Reply Quick Reply
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Need some help guys. So for ???? reasons I'm making a program that models geological systems and mineral formation. Does anyone know of a good source of information on the crustal prevalence of various minerals? I obviously can't simulate every mineral known to science, but I want to get an appropriate swath.

Much appreshes.
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trypto - Wed, 08 Aug 2018 23:15:47 EST ID:OdR7meD+ No.79199 Ignore Report Quick Reply
Oh shit, maybe this?

Here's a visualizer: https://www.clisap.de/fileadmin/B-Research/IA/IA5/LITHOMAP/
The general website:https://www.geo.uni-hamburg.de/geologie/forschung/geochemie/glim.html

Still doesn't seem to include the ocean, which seams kinda important. Maybe I'm missing something.
trypto - Wed, 08 Aug 2018 23:18:00 EST ID:OdR7meD+ No.79200 Ignore Report Quick Reply
NVM. It's still very general, and not really saying what the minerals are. But when you google for "minerals" you pretty much only get exploitable minerals.

I'll stop posting now.
Edward Cittingway - Thu, 09 Aug 2018 20:16:21 EST ID:dl9lAnzN No.79201 Ignore Report Quick Reply
Wow that's a fuckin cool link you found. Unless there's the same data somewhere in table form it's not very useful to me, but I'll probably be dicking around with it anyway, very interesting stuff.

>> You just want to know the total % of minerals, but not the geographical distribution?
Yes, then once I have percentages enough to single out the most significant minerals and soil types (scientifically significant, rather than economically) I will very crudely model what conditions cause the transformations between the different types (elemental composition, heat, pressure, water content, etc.) in order to spit out a world map that is geophysically earth-like but not the actual world If you must know, it's a map generator for a game

>>you pretty much only get exploitable minerals
Yeah that was my frustration which is why I came here in the first place. All lists are either popular/business ones that only list exploitables, or really minor geological papers that go into great minutae about some mineral that only exists in this one crater in BFE. But just by gumshoeing through that I was able to come up with a reasonable middle between the two. 'Rock-forming minerals' was the keyword that seemed to work best for me.

Anywho, thanks for the help guys. I guess we can keep talking about minerals because they are pretty rad, otherwise I will necrobump this thread if it hasn't fallen off by the time my generator is working and show you guys.
Alice Bommlegold - Fri, 10 Aug 2018 09:27:27 EST ID:28EjEn0d No.79202 Ignore Report Quick Reply
I don't know if you are familiar with Dwarf Fortress, but the guy who programmed it knows a lot about geology and has already done the same thing you are trying to do. Maybe if you ask him he will show you where to look or maybe even help you.
Edward Cittingway - Fri, 10 Aug 2018 14:52:56 EST ID:dl9lAnzN No.79203 Ignore Report Quick Reply
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Ah thanks but no, those guys are notoriously tight lipped and the complexity of Dwarf Fortress is far beyond the pale of what is necessary or would even be functional for my purposes. Besides, at this point Dwarf Fortress is well studied within the gamedev community and it's easy to get references about how it works without having to bother those two guys.

Definitely though what I am working on has some broad similarities in terms of making a world simulation that leans on emergent properties, but I'm basing it on real world science and chemistry rather than fantasy. Instead of 'mine 5 generic shits and 5 dire poops to craft 1 epic turd' it will be 'collect 75 kg water, 25 kg bacteria, 5 kg protein and 20 kg sugar to make 100 kg of epic turd'

Molecule by Lillian Dorrypedge - Fri, 13 Jul 2018 12:51:01 EST ID:1xukUjeD No.79170 Ignore Report Reply Quick Reply
File: 1531500661281.png -(11786B / 11.51KB, 505x503) Thumbnail displayed, click image for full size. 11786
Hey guys, so I am helping someone out with there organic chem class.
They have to write a syntesis for this molecule.

my question is,what is the IUPAC name for this molecule?
I can't find it online when I try the molecular formula or draw it.
trypto - Sat, 14 Jul 2018 16:27:22 EST ID:OdR7meD+ No.79174 Ignore Report Quick Reply
Is that shit real? I could see it with cyclohexane, but with a benzene ring? Looks like way too much strain. If it's real, I bet it's extremely fragile.

p - Mon, 16 Jul 2018 13:40:49 EST ID:N1w1NO9M No.79177 Ignore Report Quick Reply
concerning the synthesis
this is some pretty whack shit. you can even synth superphane but this would be way too much strain on the sp2 carbons of the benzene.

theoretically speaking its an 5-amino anhydride derivative of isophthalic acid, my best guess is that its an exercise aimed at the nomenclature or bicyclocompounds or rather heterocycles.

could you double check if you got that structure right?
Nell Binnerman - Mon, 23 Jul 2018 22:46:55 EST ID:hBAZGxou No.79189 Ignore Report Quick Reply
  • you can't put an anhydride and an unsubstituted amine in the same molecule
  • you can't link meta-separated benzene substituents unless you make an 8-or-more membered ring, because otherwise you're violating bredt's rule

that said, the compound you've drawn could be called 3-amino-6,8-dioxo-7-oxabicyclo[3.3.1]nona-1,3,9-triene. but it is impossible.

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