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10:45
@Jan @ortho @M.A.R. TRUMP WON!!! ^_^ BAWAHAHAHAHAHAHAHA!!! So @ortho, what happened to your "prediction" about Clinton winning O seer/seal? 3:)
BAWAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHAHA!
cough cough
HAHAHAHAHAHAHAHA!
cough wheeze
BWAHAHAHAHAHAHAHAHAHA!
drinks water
waits a bit
HAHAHAHAHAHAHA! X'D
@Kaumudi Nah, I didn't write KVPY ._. The Boards are scarier o.o. By the way, which exams d'ya plan on appearing for? (I'm guessing you're the type that's aiming for the engineering stream ._.) [P.S- I couldn't care less if you're a Malayali or not XD. So you don't really have to try convincing me otherwise ;)]
user228700
11:47
@AaronAbraham The boards aren't too bad. I plan on appearing for engineering entrance exams.
user228700
Well, alright then.
14:04
@orthocresol It may actually not have been appropriate for me to make the edit. There are dialects of English where 'ran' (some organic reactions are ran) would be the common usage. But, the plural "continuing"(?) passive of run in this case is some organic reactions are run in standard English.
</ELU diversion>
@hBy2Py I admit I don't know much about these formalisms. For the most part, I go with "how would I say it in real life?" which usually works pretty well, but fails quite badly with the more subtle aspects of the language. ;)
15:00
@orthocresol I'm rather a grammar nerd, so I can get hung up on details like this. :-)
 
2 hours later…
17:27
Is there really absolutely no reaction which happends in antara/antara approach ?
 
2 hours later…
Jan
Jan
19:40
@AaronAbraham Yes, and now I’m positively scared whether the world will survive the next four years.
Brb buying canned food and renting a bunker.
@Loong LOL
 
1 hour later…
21:33
0
Q: When does Phenolphthalein containing solution change colour?

Sanjukta GhoshWere were estimating the amount of dissolved CO2 in water using the American Public Health Association method. It was a Titrimetric Method using phenolphthalein indicator. Titrant used was NaOH and analyte was sample water. The following questions came to my mind: Why do phenolphthalein[HIn] ...

Its alright. I'm glad to receive a little consolation after being so much confused. b/w means between. Reply whenever you are free. Thank you. — Sanjukta Ghosh 9 mins ago
"http://chemistry.stackexchange.com/questions/62433/why-do-we-say-theres-no-co2-‌​present/62436?noredirect=1#comment106861_62436"
I can see two different question for the same one is that normal ?
questions
@9-BBN Huh?
@9-BBN Well OP posted two similar questions... that's it.
If they were identical, that would be reason for confusion
22:05
Well when I copy paste both links in the chat only one appears
but both links are différentes ugh
chemistry.stackexchange.com/questions/62433/…‌‌​​present/62436?noredirect=1#comment106861_62436
@9-BBN dunno, there may be some limiting mechanism
@Jan :D
chemistry.stackexchange.com/questions/62433/…‌‌​​present/62436?noredirect=1#comment106861_62436
interesting
the word present probably breaks something
http://chemistry.stackexchange.com/questions/14818/do-certain-cumulated-dienes-‌​present-geometric-isomerism#comment106867_14818
testing a comment out sorry — orthocresol ♦ 26 secs ago
Jan
Jan
I would have blamed the number initially.
chemistry.stackexchange.com/questions/62433/…‌‌​​present#comment106861_62436
¯\_(ツ)_/¯
Jan
Jan
Okay, that obviously doesn’t work. =C
@SanjuktaGhosh I add some calculation for you. I let you find the result by yourself if you're doing chemistry it would be not too hard. :-) — 9-BBN 2 hours ago
x3
I know, I’m being sneaky …
@Jan about what are you speaking?
What doesn't work ?
Jan
Jan
22:33
The link directly to the comment.
22:59
0
Q: When editing posts that are consistently or overwhelmingly written in one flavour of English, please do not change the flavour

JanI was rather unhappy with an edit to a post of mine (which I immediately rolled back as soon as I saw it). While one may debate about whether mannonic acid or mannuronic acid is formed in an oxidation of that type and the first equation was (deliberately!) incomplete I was especially unhappy abou...

1
Q: Formaldehyde from Urea?

MartinI was wondering if it is possible to make formaldehyde (1) from urea (2). I noticed that they have a similar structure, but the two hydrogen atoms in formaldehyde are replaced with two amide groups in urea. Would it be possible to remove those groups and replace them with hydrogen?

I am thinking I found something which works I found a great publication about reduction of carbonic acid derivative but is my first step probable ?
Jan
Jan
Yes. Although the reaction will proceed very slowly.
3
Q: Is it possible to crystallize and extract electrons

xyz123Okay, I know that this reads ridiculous insane, but one can obtain solvated electrons by adding sodium metal to liquid ammonia solution. The chemical reaction as written in my inorganic chemistry textbook is this: $$\ce{Na + x NH3 -> Na+ + e(NH3)_x-}$$ A metallic sheen is observed, and it su...

ಠ_ಠ
That title is ridiculous
Then I use NaOH to keep only one of both hydrogens and using $[Fe(H)(H_2)(PP_3)][BF4]$ in H2O/THF (10/1) 80°C, 5h we must obtain HCOOH with a yield of 88%
I forget the $H_2$ at 60 bars
:D
forgot
ugh
english ..
23:17
@pentavalentcarbon Hmm... Whole post could be rewrited with proper stuff but...
there's some stuff in it that I don't understand
seems pretty neat though
And here comes better title
I almost like the sensationalist one more
pretty good for "chemistry clickbait"
@pentavalentcarbon :)
Well I have read carefully so i can't do like the did
But can I use LiAlH4 to obtatin HCOH from carbonic acid ?
I'd like to say yes but I'm not sure
23:29
@9-BBN o.O
Did I say something wrong ? ^^
You've got to be kidding me
How on Earth did you get that idea
Nucleophilic attack of hydrid in C=0 then release of OH- because LiAlH4 is very very basic
And once again
:D
HCOH is a carbene... and... and... Just no, you can't
No
I said
HO(CO)OH + LiALH4 will give HCOH
23:35
You mean formaldehyde?
I mean doing this
Can't get it too
Why ?
So I have an alternative which shows at least I know a bit of organic chemistry ^^
And write it H2CO or CH2O but not like this
From urea I can do Eschweiler Clarke methylation in both side. Then I will have a bi Weinreb amide then I use LiAlH4
But it doesn't tell me why what I thought about carbonic acid to methanal can't works ^^
What is fun with my Eschweiler Clarke is that I will need methanal to synthesis after some step...methanal
23:41
You'd get sodium carbonate. Then maybe it would be further reduced but you wouldn't be able to control
You generally don't make aldehydes with strong reductants
The Eschweiler–Clarke reaction (also called the Eschweiler–Clarke methylation) is a chemical reaction whereby a primary (or secondary) amine is methylated using excess formic acid and formaldehyde. Reductive amination reactions such as this one will not produce quaternary ammonium salts, but instead will stop at the tertiary amine stage. It is named for the German chemist Wilhelm Eschweiler (1860–1936) and the British chemist Hans Thacher Clarke (1887-1972). == Mechanism == The first methylation of the amine begins with imine formation with formaldehyde. The formic acid acts as a source of hydride...
You sure ? ^^
Whatever... Why would anyone synthesize methanal?
This is a question
Iwill propose an answer even if this is awfull to do that
Have you ever read in mathoverflox "awfully sosphisticated proof for simple facts"?
This is brilliant lol
Whatever... g'night!
See you

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