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03:02
!!img/silver perchlorate
 
5 hours later…
08:08
!!img/squalene
!!img/squalane
!!img/squarane
No result found.
08:08
!!img/cubane
!!img/dicubane
No result found.
!!img/nitrocubane
08:09
!!img/octanitrocubane
!!img/tesserene
No result found.
 
1 hour later…
09:27
is it more efficient to do esterification through the conc. H2SO4 pathway or the acyl chloride pathway?
10:01
We can react acyl chloride with ammonia to form amine... can't we remove an amine group?
 
1 hour later…
11:15
@Kaumudi.H Ohhhhhhhhhhhh! That one...I'm still cracking up over that! X'D
user228700
Sure -_-
For reasons, I don't really understand, I feel immensely gratified when I'm able to piss you off :D
user228700
Alas, although I may come across as pissed off, I don't give almost random strangers on the internet any power over my feelings :-]
@Kaumudi.H Hey, it's just that you tend to over-react to stuff I say...whatever I said/typed, it was in jest. Geez, I'm sorry if you're the extremely delicate type ;P
@Kaumudi.H O_o
@Kaumudi.H That last edit was scary :O
user228700
@paracresol I'm not sure whether that ^ is an apology or if it's another one of your attempts to piss me off. In any case, it's okay. I'm certainly not as delicate as you think. Perhaps it's just your tendency to try to piss me off that really sort of annoys me. Almost. Whatever :-P
11:22
@Kaumudi.H It was an apology ._.
user228700
I feel that sometimes, you say provocative crap just to see if I would react :-P But I don't know if that's really the case or if we're genuinely complete opposites in literally every way.
( @ortho's watching this from his corner...I hope I don't get suspended -_- )
@Kaumudi.H Nope, we're definitely opposites ._.
user228700
Okay :-P
So, moving on to more important things...
I'VE GOT MORE HAT'S THAN YOU! HAH!
user228700
:-) I didn't try. @SirCircumference is really the only reason I've got at least 9 hats.
11:26
@Kaumudi.H Um...well... my top hat's shinier than yours ;D
user228700
@paracresol So this is an attempt to lighten the mood(a.k.a crack a joke)?
@Kaumudi.H Nope...that's just me trying to piss you off X'D
user228700
x'D Aha! Exactly!
user228700
I'm sorry to burst your bubble man, but I honestly don't get pissed off that easily.
user228700
Oh, and I assume that ur denial of my gender is also an attempt to piss me off? x'D
11:28
@Kaumudi.H Was that an invitation to try harder?
user228700
@paracresol Invitation is the wrong word--it's up to you.
user228700
Why tho? Why are u trying? :-P
@Kaumudi.H Nah, most people I talk to often here are human males ( at least I hope @Jan is ) so I "accidentally" keep referring to you as a "he" :/
@Kaumudi.H What makes you think I'm trying? 3:D
user228700
4 mins ago, by paracresol
@Kaumudi.H Nope...that's just me trying to piss you off X'D
Jan 1 at 17:18, by paracresol
@Kaumudi.H Yup, you've got wonderful memory :3
user228700
11:33
Nah, that's just me trying not to be absent-minded, boi.
user228700
Anyhoo, how's prep.?
It's ...going ._.
Boards this March, wish me luck!
On second though...don't
user228700
What? Why not? .__.
user228700
U're Bio Math, right? (Since u were complaining about Math before)
user228700
Are ur practical exams over?
13:25
Is there correlation between strength as nucleophile and strength as base?
13:44
edited !
@DHMO As long as the donor atom is the same, there is a general correlation.
However, consider HS- and HO-. HS- is a better nucleophile but HO- a better base.
@orthocresol is ethoxide a strong base but a weak nucleophile?
Ethoxide's a pretty decent nucleophile in its own right
@orthocresol why is HS- a better nucleophile?
strong base promotes elimination (E2) while strong nucleophile promotes substitution (SN2)?
Sulfur's 3p orbitals are higher in energy than oxygen's 2p orbitals.
Consequently, there's a better energy match with the empty orbitals of an electrophile.
And yes, in general, that is the case with E2 vs SN2.
13:53
but if there is a correlation then... they pretty much happen 50-50?
Yes, it's possible to get a mixture of products.
So we would need to use concentration (of base/nucleophile), heat, and solvent to control the favoured product?
Yeah, pretty much.
thank you
4 hours ago, by DHMO
is it more efficient to do esterification through the conc. H2SO4 pathway or the acyl chloride pathway?
Depends on your molecule. Chucking conc H2SO4 at a molecule may not always be the best way to go.
13:58
e.g. ethanoic acid + ethanol?
oh well, that one you can use anything you like
then what are the circumstances that we cannot use the conc. H2SO4 pathway?
if you have something that is acid-sensitive
oh, like a carbon-carbon double bond?
say, idk, an epoxide?
14:00
I know nothing about epoxides lol
4 hours ago, by DHMO
We can react acyl chloride with ammonia to form amine... can't we remove an amine group?
 
4 hours later…
18:01
0
Q: Rates of Keto-Enol Tautomerism

XBBAre there any databases with rate constants for keto-enol tautomerism in small molecules? I'm looking for rate constants if possible.

 
3 hours later…
Jan
Jan
20:40
@paracresol Not sure if I should be sad, happy, glad or laughing.
Hm, someone was removed again.
21:00
@Jan Did it hurt your reputation?
@Loong Looks ron lost over 100, but is it much difference fo him...
$b = 4 \text{Volume}_{molcule} \times N_a$ or $b = \text{Volume}_{molcule}\times N_a$. b is van der waal constant. ?
21:23
@A---B The usual interpretation is four times the volume of the particle.
Jan
Jan
@Loong Yeah, I lost about 0.2 % of my rep ;)
21:57
> Apparently, compounds with a higher molecular mass have a boiling point.
That's correct, but I think the sentence is missing a word. ;-)
@Loong :D

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