| Search |
| [Next Page] |
Sodium Borohydride identification/verification?
[rquote=334896&tid=30736&author=UnintentionalChaos]That seems really excessive compared to j ... |
17-6-2014 at 21:07
by: FireLion3 |
24/40 x 200mm Leibig on eBay - Unbelievable Deal $10 + Free Shipping
Glassware from China is always excessively low price. Correction, almost everything from China is al ... |
17-6-2014 at 15:09
by: FireLion3 |
What could Benzene be worth, sold by the liter.
There are several chemical supply companies in the USA that sell Benzene. Here is a rough list of pr ... |
17-6-2014 at 14:47
by: FireLion3 |
Testing the purity of a nitrate salt
Is there a reason you just don't buy it pure? Both Ammonium and Potassium Nitrate can be bought rela ... |
17-6-2014 at 14:39
by: FireLion3 |
Why do people go out of their way to gas organic bases when forming salts?
As opposed to just pouring in the aq. acid?
Crystals do not precipitate in water, but the base is ... |
17-6-2014 at 13:54
by: FireLion3 |
Thermometer adapter seal?
Yes, but even with this site you linked, they don't appear to have different sized "fitments". I hav ... |
3-6-2014 at 21:46
by: FireLion3 |
How do the reductive properties of Zinc and Zinc Amalgam differ?
[rquote=332541&tid=30450&author=Nicodem][rquote=332488&tid=30450&author=FireLion3]Zi ... |
29-5-2014 at 20:58
by: FireLion3 |
How do the reductive properties of Zinc and Zinc Amalgam differ?
Sure, but the Clemmensen Reduction is but one of the infinite uses of zinc as a reducing agent. My r ... |
27-5-2014 at 10:22
by: FireLion3 |
How do the reductive properties of Zinc and Zinc Amalgam differ?
Both are used as reducing agents but the Zinc Amalgam is considered to be more powerful. Beyond this ... |
27-5-2014 at 09:05
by: FireLion3 |
Distilling to dryness under a vacuum - is there a safe limit?
So then how does a person go about isolating a target compound when the rest of the reaction mixture ... |
20-5-2014 at 20:33
by: FireLion3 |
Distilling to dryness under a vacuum - is there a safe limit?
Is there any safe limit in doing so? If, for instance the temperature of the flask never exceeds 50 ... |
19-5-2014 at 19:59
by: FireLion3 |
Aluminum Amalgams, radical chain initiation - is water a requirement?
I'm planning to use a pre-prepared Aluminum Amalgam to cause an irreversible electron transfer to an ... |
15-5-2014 at 19:54
by: FireLion3 |
uk Ebay seller busted
I'm surprised they are walking around free right now. Selling half of that stuff in the US will get ... |
11-5-2014 at 12:02
by: FireLion3 |
On a simple aryl alkyl terminal alkene, which bonds are more nucleophilic?
Would the double bonds of the aromatic ring be more nucleophic due to shared electron resonance, or ... |
11-5-2014 at 03:00
by: FireLion3 |
What happens to the acyl group in a base-catalyzed deacetylation?
Ah, that makes sense. So, the hydroxide is not used as a catalyst but as a reactant? Meaning calling ... |
9-5-2014 at 11:28
by: FireLion3 |
What happens to the acyl group in a base-catalyzed deacetylation?
How? A carboxylate ion has two oxygen (according to wiki). Acyl group only has one. |
9-5-2014 at 11:15
by: FireLion3 |
What happens to the acyl group in a base-catalyzed deacetylation?
A base catalyzed deacetylation reaction can occur if an acyl group is conjugated or nearby other ele ... |
9-5-2014 at 10:30
by: FireLion3 |
How stable are formaldehyde imines in aq. solutions?
See, that is a very interesting piece of information. Out of all the pages I looked at regarding the ... |
6-5-2014 at 19:13
by: FireLion3 |
Silly question about solvents...
This is probably a very silly question but I have pondered it for quite some time.
Is the use of ... |
5-5-2014 at 08:02
by: FireLion3 |
How stable are formaldehyde imines in aq. solutions?
Does this happen due to the imines general solubility in organic solvents, causing it to be mostly s ... |
5-5-2014 at 07:52
by: FireLion3 |
How stable are formaldehyde imines in aq. solutions?
I've been finding a ton of conflicting information on this topic regarding monomethylations and dime ... |
4-5-2014 at 13:11
by: FireLion3 |
Using the Acetone enolate from Sodium Hydroxide
[rquote=327589&tid=30097&author=Cheddite Cheese]Is sodium hydroxide a strong enough base (co ... |
14-4-2014 at 09:02
by: FireLion3 |
Using the Acetone enolate from Sodium Hydroxide
[rquote=327567&tid=30097&author=adamsium]I actually did the aldol condensation of acetone an ... |
14-4-2014 at 02:44
by: FireLion3 |
Using the Acetone enolate from Sodium Hydroxide
Interestingly, I keep finding things like this:
[url=http://books.google.com/books?id=AcpPyv0HWRsC& ... |
13-4-2014 at 22:38
by: FireLion3 |
Using the Acetone enolate from Sodium Hydroxide
[rquote=327504&tid=30097&author=leu]The pKa of acetone is about 19 
Chemists have been c ... |
13-4-2014 at 18:41
by: FireLion3 |
| [Next Page] |
