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12:10 AM
@Jan you said much more than one step what do you think of that
 
 
1 hour later…
1:19 AM
3
Q: Structure of Sodium Naphthalenide

Eashaan GodboleThis question is a sort of follow-up to my earlier question. I know about a method of solubilising potassium where the potassium atoms are "trapped" between layers of graphite, but I think that sodium naphthalenide exists only in solution (if a contradiction is found, please inform). In the sol...

 
 
3 hours later…
user228700
4:07 AM
Hey everyone :-)
 
user228700
I've a quick question. Whilst drawing resonance structures, why is that structures that have smaller separation of opposite charges are more stable than those structures in which opposite charges are delocalized on atoms that are farther away from each other?
 
user228700
My textbook explains this by saying that it requires energy to separate opposite charges...but why?
 
user228700
Googling has not yielded any answers :-|
 
user228700
Also, erm, my textbook has given a few guidelines to select the most stable structure of all the resonance structures and these are:
 
user228700
 
user228700
4:17 AM
But how am I to prioritize among these rules?
 
9:21 AM
@9-BBN huh? That's not a Weinreb amide...
 
@Kaumudi coulomb's law
 
Hey guys,Is anyone of U active on academia??I have got a problem there.
 
5
A: Structures for NO+ (Nitrosonium)

orthocresol Which is a better Lewis structure? There is no such thing as a better or a worse Lewis structure. They should be properly referred to as major or minor resonance contributors/forms. I looked up a textbook to check the rules of determining which resonance structure contributes more. The orde...

 
@Kaumudi why would you need to?
 
user228700
@DHMO To rank canonical structures based on their stabilities.
 
9:30 AM
0
A: Problem digesting sample for Ti analysis using ICP-OES

Stian YttervikSo, posting here since I can't comment due to lack of rep. When you say "trouble digesting" what is you trouble? You say the analyses come out other than expected, but do you mean "the solution is cloudy". Is this a fact? If the solution is clear it can still be a digestion problem for certain bu...

 
@Kaumudi there are actual questions that ask u to do so?
 
user228700
@DHMO Yeah.
 
guys please answer
 
People never cease to amaze me
"I don't have enough rep to post a comment, so that must justify me posting my comment as an answer"
 
user228700
@DHMO Ah, OK.
 
user228700
9:33 AM
@DHMO: No clue?
 
user228700
Ooh BTW, is anybody here familiar w/ Moseley's Law?
 
@ kaumudi,are u reading soloman and fryhle??
 
20 mins ago, by orthocresol
@9-BBN huh? That's not a Weinreb amide...
@orthocresol yes you're right i forgot the OMe on the N in Weinreb amide
But it looks like ^^
 
user228700
9:53 AM
@THELONEWOLF. Yes.
 
11:18 AM
0
Q: What's our (maybe updated) take on questions about (quantum) chemical software?

Martin - マーチンFrom What topics can I ask about here? Some kinds of questions aren't allowed here: Computational questions: If your question is purely about numerical methods you are using in a simulation/etc, it is probably more appropriate at Computational Science. Recently (or maybe not) I n...

 
11:45 AM
@ringo maybe they just want to speak
 
 
2 hours later…
1:56 PM
@Jan Ha! I already have a bunker ;) de.wikipedia.org/wiki/F%C3%BChrerbunker
Heyyy! Trump isn't that bad ._.
@Kaumudi That might depend on how you define 'familiarity' o.o
@Kaumudi Curiosity question: Are you a Pinarayi mol or a Chandy mol?
Politics is the inevitable destination of every conversation
 
user228700
2:20 PM
@AaronAbraham I...don't know anything about politics in Kerala, sorry.
 
2:45 PM
@Kaumudi Of course you wouldn't know. After all, you aren't a Keralite, right ;)
Fine then @Kaumudi , who were ye mooting for? Trump or Clinton? [I was the only one in my class mooting for Trump as President, but every other guy in the class wanted Pullimurughan for President X'D]
Oh right! You aren't a Malayali. Just so that you know, Pullimurughan is the Malayali equivalent of Kabali ;D
"Not a Malayali", God I love rubbing that in 3:)
 
user228700
3:13 PM
@AaronAbraham No, I am not. I don't even like Kerala all that much. I'm a Malayali but I identify as a Chennaitee because I've lived here my whole life.
 
user228700
@AaronAbraham Hilary-the lesser of two evils.
 
@Kaumudi ಠ_ಠ
She's the only one that's evil there ;P
@Kaumudi :O
Treason
ಠ_ಠ
Lived there your whole life? Darn, your life must've sucked XD (no offense)
@DHMO o/
 
@AaronAbraham Guten Tag
 
Well at least ya didn't Guten Tag me this time, so I guess that's an improvement ;)
 
user228700
@AaronAbraham I'd like to extricate myself now, from what may possibly be a heated argument about why Chennai has been better to me than Kerala.
 
3:21 PM
@DHMO It's been a while since a ran into ya ._.
 
@AaronAbraham I'm just in the math chat room
 
@Kaumudi Whoops, typing error! You mean "Kerala better than Chennai", right? XD
 
user228700
*To me.
 
._.
@DHMO And to think I thought this was the Chem. chat room. Must be those mushrooms I ate ._.
So @Kaumudi, JEE or some regional exam?
 
user228700
@AaronAbraham JEE.
 
user228700
3:23 PM
Gots to go now. Bye!
 
@THELONEWOLF. Seems to be all over you; guess that explains it ;)
@Kaumudi Tschüss
> Kaumudi,are u reading soloman and fryhle??
@Kaumudi Honestly, what d'you think you're chances of making it to the top 500 are?
Curious
 
Does anyone here have experienced with the exabyte platform?
have experience*
 
@AaronAbraham have i asked you where you are from?
 
3:40 PM
@Chemobot Do you still talk?
 
!!greet/@QuantumCAPUCCINO
 
Welcome to The Periodic Table @QuantumCAPUCCINO! Here are our chat guidelines and it's recommended that you read them. If you want to turn Mathjax on, follow the instructions in this answer. Happy chatting!
 
That's neat.
!!greet/@DHMO
 
Welcome to The Periodic Table @DHMO! Here are our chat guidelines and it's recommended that you read them. If you want to turn Mathjax on, follow the instructions in this answer. Happy chatting!
 
@AaronAbraham,I can't get you.what r u trying to say??
 
3:48 PM
!!greet
!!greet/
 
Welcome to The Periodic Table ! Here are our chat guidelines and it's recommended that you read them. If you want to turn Mathjax on, follow the instructions in this answer. Happy chatting!
 
!!dance/
 
@Chemobot,was it for me??
 
user228700
4:50 PM
@AaronAbraham I don't know, man.
 
5:15 PM
Top 500 in what??
 
 
1 hour later…
 
1 hour later…
Jan
7:56 PM
@9-BBN It somewhat defeats the point to use a compound as catalyst that you’re trying to synthesise three steps later :D
@Martin-マーチン Hee~y, I’ve almost got a finished introduction, which means a finished text (except for an abstract … that should be done tomorrow™ …)
@Loong Probably … just doesn’t make sense otherwise …
 
@jan about what are you speaking ?
Oh
Sorry
Yes this is really awkward
:D
I am working on a better idea but 1)organic chemistry is not my cup of tea even if I like it and 2) I'm just a student without a lot of experiments so
 
Jan
!!tea
 
For two ?
!!ricin
!!ricine
!!img ricin
 
Jan
8:16 PM
!!img/ricin
?
 
No result found.
 
:O
@Chemobot do you know BreakingBad ?
 
@Jan That thing has more than 60 kDa. Do you really want the poor bot to draw that structure? ;-)
 
The structure is on wiki ^^
 
Jan
@Loong It’s not like the bot is drawing anything, it totally just steals it from the interwebs ;p
 
8:19 PM
 
8:41 PM
@Hippalectryon Yo ca va ?
!!/img EDTA
 
@9-BBN oui et toi ?
 
Moi ca va plutôt bien, tu es toujours en stage militaire
Ah le bot a du mal avec l'EDTA ...
 
@9-BBN oui
!!img/edta
 
J'ai tapé à l’envers la commande ^^
 
8:49 PM
:P
 
Et ça consiste en quoi ?
 
Jan
@9-BBN Tu dois écrire img/{nom du molécule}. Tu le fais incorrectement tous les temps !
 
fais*
:P
 
@9-BBN Pour l'instant je suis en école d'officier de la gendarmerie, j'entre en unité pour 4 mois dans deux semaines
 
Jan
(I know my French is horrible if I don’t spell check five times minimum! ;p)
 
8:50 PM
@Jan I though first it was Hyppa ^^
 
@Jan Your French looks really natural though !
 
Jan
\o/
 
Tu = s at the end :)
@Hippalectryon et ça te plaît ? :P
 
Jan
@9-BBN In theory I know, yeah … although x = s ;)
 
Yes :)
 
8:52 PM
@9-BBN Il y a des moments plus intéressants que d'autres... mais ça va dans l'ensemble. En revanche l'absence de wifi me rend triste :-(
 
Ahahaha le pauvre sans internet il est perdu :P
 
Jan
(inb4 @M.A.R. unstars that for being foreign xD)
 
@Hippalectryon does the bot can draw molecules in three dimensions ?
(the)
!!img/buckminsterfullerene
 
@9-BBN chemspider doesn't provide 3D pics of molecules; it does provide a 3D app in which we can interact with the molecules, but the SE chat doesn't support it
 
8:56 PM
It does ! :D
but in 2D :P
It would be fun if it was possible to keep only one ion in a footballene to have a positive or negative charge alone
Or use them to make 100% yield enantioselective reactions
As big endrance group
 
hindrance*
 
hindrance
Yeah in en hin an the same with a gum in mouth
 
Jan
I just upvoted ;)
 
LOL
Only because it is in two step
steps
 
9:56 PM
@orthocresol what do you think if I use sciencedirect.com.sci-hub.cc/science/article/pii/… urea with two eq acetone then LAH ?
I also though of Wittig with =PPh3 then Eschweiler-Clarke after LAH and to finish O3 with PPh3
 
10:15 PM
why acetone? You'd be sticking an isopropyl group on the nitrogen that way.
Oh, I see. The alkyl group doesn't matter.
As I said, I don't buy the LAH reduction. I'm not sure, it might work, but I'd need to be convinced a bit more.
 
Jan
If LAH overshoots, just Swern or DMP the resulting methanol. No?
 
¯\_(ツ)_/¯
Fair enough..
 
Well what would you do with LAH ?
Oh
methanol hum
 
I don't know what ozonolysis does to terminal alkenes.
and I'm a bit lazy to look it up right now
 
If we take exaclty enough LAH to make the reaction why do methanol
 
10:19 PM
the moment you make any formaldehyde, LAH is going to attack it instead of the amide (which is much less electrophilic)
 
Jan
Terminal alkenes are ozonolysed just like internal ones.
But OsO4/NaIO4 could be equally viable.
 
fair enough - because (usually) people care about the other side of the alkene instead of the CH2 part ;)
IIRC with oxidative workup you get CO2, but again not sure
 
So if it is possible I have a cycle to propose with urea as catalyst lol
 
don't see any reason for that with PPh3 or Me2S
 
Jan
Yeah, you should use PPh3 workup.
 
if i remember correctly
and yes, that is the "other side of the alkene" that i'm talking about, if you notice, it doesn't say R = H only R' = H
 
But what about the second part of the C=C bond ?
 
that's what you're supposed to show
not saying that you're wrong, i'm just saying that screenshot doesn't tell you what happens to the CH2 part
 
Then I can use an other phophorus ylure
And it will be ok sure :)
Eschweiler-Clarke will work with the enamine ?
 
idk, i'm not very interested in this "synthesis" tbh
but if you wanted to methylate urea, i'd just use NaH and MeI
 
10:32 PM
OK, I do it for fun also it makes me revising my lesson for the last exam of organic chemistry I'll have for all my life
I want to do it as a master ^^
 
true true, but getting to formaldehyde is pretty difficult..
lots of selectivity problems
all the best, i've gotta go off now
 
I like challenge. Also I will make other proposition in the answer and people who wants will continue by themselves
 
exam season now? so many HW questions...
 
HW ?
I have a continuus control in my school
I did an exam two weeks ago and I'll have a second one in two.
First one was for 20% of the final mark, the next will be for 35%.
 

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