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Natural Science Forum / Chemistry / Organic Synthesis / September 2003



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ThreadLast Post  Replies
Does carbon form quadruple bond?30 Sep 2003 18:14 GMT7
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, resonance30 Sep 2003 18:11 GMT3
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 GMT1
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 hydrogenation17 Sep 2003 15:30 GMT3
                                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 esters17 Sep 2003 15:29 GMT2
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 & Levo12 Sep 2003 20:41 GMT6
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 acid10 Sep 2003 15:24 GMT4
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 anthranilate09 Sep 2003 18:15 GMT2
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 alcohol08 Sep 2003 17:45 GMT9
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 ...
 
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