| Search |
What is it about aromatic rings that induce non-polar properties on polar chains?
So essentially this:
[quote]Aromatic molecules typically display enhanced chemical stability, com ... |
17-5-2014 at 13:19
by: JefferyH |
What is it about aromatic rings that induce non-polar properties on polar chains?
I've noticed that a lot of molecules with aromatic rings tend to behave as though they are non-polar ... |
17-5-2014 at 12:05
by: JefferyH |
Washing an organic solvent of potassium bromide with water?
If I understood why potassium salts are soluble in some organics this would be a lot easier. If I co ... |
17-5-2014 at 11:27
by: JefferyH |
Boiling off water formed by reaction of hydroxide with carbonyl?
If my substrate before deprotonation has a higher bp than water, and is dissolved in another high bo ... |
16-5-2014 at 21:51
by: JefferyH |
Washing an organic solvent of potassium bromide with water?
Quite a lot of water....! But yes, this does sound like a viable idea.
If I can't get it all out ... |
16-5-2014 at 19:19
by: JefferyH |
Washing an organic solvent of potassium bromide with water?
[rquote=331482&tid=30387&author=The Volatile Chemist][rquote=331480&tid=30387&author ... |
16-5-2014 at 19:03
by: JefferyH |
Washing an organic solvent of potassium bromide with water?
I have an unknown organic solvent that is not miscible with water. Dissolved in 1L of it are 600g of ... |
16-5-2014 at 18:28
by: JefferyH |
Reactions in liquid ammonia? Thermal/Kinetic issues?
Okay, thank you. Such a simple concept finally made clear . Just had to clear
that up.
By the wa ... |
15-5-2014 at 16:36
by: JefferyH |
Reactions in liquid ammonia? Thermal/Kinetic issues?
Yes, but would these reactions 'exponentially faster' if brought to a higher temperature, such as un ... |
15-5-2014 at 15:57
by: JefferyH |
Reactions in liquid ammonia? Thermal/Kinetic issues?
I was reading about various reactions in liquid ammonia and their benefits. Some studies refer to "r ... |
15-5-2014 at 14:52
by: JefferyH |
Do stronger bases create stronger nucleophiles?
Sorry I don't have a digital copy. I have in front of me a brief physical copy of a paper we were gi ... |
15-5-2014 at 10:25
by: JefferyH |
Do stronger bases create stronger nucleophiles?
Here's a question. I was going to make a new thread for this but realized it could be tied into this ... |
14-5-2014 at 22:04
by: JefferyH |
SN1, competition reaction of substrate and product to react with base? - Word Problem Help
I'm looking at a worksheet right now and this word problem I can't quite seem to figure out.
[ ... |
12-5-2014 at 10:35
by: JefferyH |
Is the avoidance of rapid distillations needlessly over-emphesized?
72L!!! That's crazy! I imagine the hardest part of that process was handling the glassware. Are that ... |
8-5-2014 at 19:58
by: JefferyH |
Do stronger bases create stronger nucleophiles?
That's what I assumed but I wasn't entirely sure. That helps a lot! Thanks! |
8-5-2014 at 19:50
by: JefferyH |
Do stronger bases create stronger nucleophiles?
Very nooby question... I know....
If there is a compound that can be deprotonated by a base to gi ... |
8-5-2014 at 18:55
by: JefferyH |
Is the avoidance of rapid distillations needlessly over-emphesized?
I probably will be using 5L flasks and splitting up the distillation. I don't see any reason to over ... |
8-5-2014 at 18:54
by: JefferyH |
Solvent miscibility of 3 different solvents, 2 miscible, one not?
So for the sake of molecular interactions, is it a safe assumption that there will always be a great ... |
8-5-2014 at 11:01
by: JefferyH |
Solvent miscibility of 3 different solvents, 2 miscible, one not?
Sorry for the vague title. I haven't been able to find a good answer for this question so I figured ... |
8-5-2014 at 10:53
by: JefferyH |
Is the avoidance of rapid distillations needlessly over-emphesized?
[rquote=330453&tid=30320&author=deltaH]Entrainment is typically only a minor contaminant, pr ... |
8-5-2014 at 00:58
by: JefferyH |
Is the avoidance of rapid distillations needlessly over-emphesized?
Is there any correlation between entrainment and the difference in the BP's of the substrates? Not s ... |
7-5-2014 at 23:54
by: JefferyH |
Is the avoidance of rapid distillations needlessly over-emphesized?
I always hear that distillations should be taken slowly, which is understandable in certain circumst ... |
7-5-2014 at 20:21
by: JefferyH |
