Dresden's Chemical Fluff Thread (Name-A-Molecule)

[Gaffy]

BOGGART

It will turn into your biggest fears..

(Not a Gaffy's, not to be ever taken by anyone, unless you partake in ritualistic usages of fearsome hallucinogens, which I don't recommend
)

TAZERINE

It won't get you down

 

[Rectify]

GLOW STICKS
2,4,6-trichlorophenyl-carbonyloxy-2,4,6-trichlorobenzene

See You On The Playa This Coming Labor Day Of Love!!!

 

[Gaffy]

Mike Tyson V Trevor Berbick

Alpha players game.

 

[Gaffy]

GLOW STICKS
2,4,6-trichlorophenyl-carbonyloxy-2,4,6-trichlorobenzene

See You On The Playa This Coming Labor Day Of Love!!!

What do you think it would do?

 

[sekio]

^ isomeric trichlorobenzoic acids (2,3,6 trichloro) are used as herbicides, acting as auxin analogs.

2,4,6-trichlorophenol is a general biocide (kills everything) that is related to the active ingredient of Dettol antiseptic (chloroxylenol) and also a presumed carcinogen.

2,4,6-trichloroanisole (the methyl ether of 2,4,6, trichlorophenol) is a metabolite of trichlorophenol made in fungus, and has a strongly unpleasant odor. It is found as a flaw in winemaking known as "cork taint".

A closely related compound, the oxalate bis-ester of trichlorophenol, is used as a major component of chemical light sticks, in combination with a fluorescent dye, a weak base, and hydrogen peroxide. That explains the "glow sticks" name.

 

[Gaffy]

I see ^^ Still, wouldn't be very pleasant imo

 

[Gaffy]

sulfate does not have that structure that would imply the fully protonated form would be H₄SO₄.

"Methyl-tom and methyl-jerry" ?

I knew I wasn't wrong!; look!

 

[sekio]

That's still an incorrect structire for sulfuric acid.

 

[Gaffy]

I'll make sure to tell the french science academy
Just kidding..
That's where I have it from.

 

[polymath]

That structure describes an electrically neutral sulfuric acid molecule, with the polarity of the chemical bonds shown as the S having a charge of +2 and the oxygens having charge -1. It's probably easy to see only the "+" or "-" charges and think that is supposed to be a structure of a sulfate ion. I think that is the source of confusion here.

 

[Gaffy]

What if it is used with R-CNH2 which is neutral, the + should go to the N and the - play its role of acid, like HCL

 

[Gaffy]

In which case my drawing is indeed wrong, as it should be NH2 and SH204, both "neutrally charged"

 

[polymath]

What if it is used with R-CNH2 which is neutral, the + should go to the N and the - play its role of acid, like HCL

Here's a picture of amine protonation

 

[Gaffy]

So it goes from this:

To this:

Damn.. I understood wikipedia was wrong when counting hydrogen from the first picture's reaction to this, which is wrong

Can a positive charge replace a hydrogen chatge in the third example?
Thus not saying the french wikipedia is wrong? "

 

[Gaffy]

On topic:

LOADYLOL

Get a good load of lols.

SINDANE

Just Because this little fucktard sucks

 

[Gaffy]

EPHYLONE the second

8-Ethyl-7-PHenYLoctahydroindOliziNE

 

[Rectify]

TRY ME
1-(3,4-dihydroxyphenyl)-2-aminopropane

 

[sekio]

putative neurotoxin? no thx

 

[negrogesic]

Steve Urkelamine, the nerdiest dopamine agonist on the block.

 

[Rectify]

DISSO
2-ethylamino-2-(3-oxocyclohexyl)-1-oxocyclohexane