| Thread | Last Post | Replies |
|
| Does carbon form quadruple bond? | 30 Sep 2003 18:14 GMT | 7 |
I do know about the hybridization theory and I do know about the VSEPR theory, and that according to bond angles it is very unlikely for carbon to bond to other atom with a quadruple bond. This would require much energy to synthesize and if done, it would not be stable, but, is
|
| hyperconjugation, resonance | 30 Sep 2003 18:11 GMT | 3 |
what is hyperconjugation? how it affects the stability of carbocation and carboanion? is resonance true or imaginary?
|
| who can help me? | 29 Sep 2003 15:21 GMT | 1 |
I am a undergraduate student . I need a free websit which can download e-book that is about to "advanced organic chemistry".I long it very much with which I can complete my homework. Who can help me ?
|
| acids for catalytic hydrogenation | 17 Sep 2003 15:30 GMT | 3 |
I'm want to conduct a catalytic hydrogenation under acidic conditions. The reference uses traces (0.5 mL per 20 mL solvent hexanes) perchloric acid (HClO4), which for safety reasons and the lack of a washdown fumehood, I cannot and don't want to use ...
|
| Informations about allyl esters | 17 Sep 2003 15:29 GMT | 2 |
Hi Group! I'm looking for any consolidated information/materials/books about allyl esters and their properties. It's quiet hard to find something about it, even in internet ;-)
|
| Cis, Trans, Dextro & Levo | 12 Sep 2003 20:41 GMT | 6 |
Let's say one wishes to make an organic amine by a Hofman alkylation (RX or PhRX + NR2). The alkyl halide is not available commercially, so it must be made from a alkene by hydrohalogenation. The alkene comes in cis or trans forms.
|
| Carbon-13 enriched trifluoroacetic acid | 10 Sep 2003 15:24 GMT | 4 |
Uranium is enriched as the more volatile UF6. Since 13C chemistry is so expensive we need to think through our options, carefully. We need trifluoroacetic acid enriched (at least) at the 2 position. Natural abundance TFA is cheap in quantity. The formula weight of TFA is 114
|
| phenyl anthranilate | 09 Sep 2003 18:15 GMT | 2 |
Just to make life hard: I need to synthisize about 5g of phenyl anthranilate for a uni lab project. Can some one please check or comment on this method our group came up
|
| Re: drying alcohol | 08 Sep 2003 17:45 GMT | 9 |
what do you need this for? If it is for lab scale reactions then just buy some dry Ethanol from your normal lab chemical supplier. It can't be done as easy as you think. A commercial process uses beds of molecular sieve at temperature to remove the water. Other methods are pressure ...
|