denoza
ENTUZIJASTA→ Poznavalac
okt 2015.
Stipe
ZMAJokt 2015.
In the first step, the heat applied excites the molecule and causes the carbon-carbon bond between the benzene ring and the carboxyl group to break and reform on the oxygen molecule in the hydroxyl part of the carboxyl group. This causes the electrons from the O-H bond to move to the hydrogen. There is now a negatively charged hydrogen ion with a lone pair and a carbon dioxide molecule, along with a THC molecule with a positive charge on the member of the benzene ring that the carboxyl group left from.
Once this happens, the hydrogen ion moves in to bond with the carbon in the benzene ring, forming THC. We now have an active THC molecule and a carbon dioxide molecule produced from an biologically inactive THC acid.
I'm guessing that this happens via an SN1 reaction because the carbocation intermediate that is formed is relatively stable due to the positive charge not just being in the benzyllic position, but actually in the benzene ring.
Ovo ne mora biti tocno. Samo spekulacijeVutra Samotnjak
ZMAJStipe
ZMAJokt 2015.

PowerSeed
ZMAJokt 2015.
savagestrain
AMBASADOR→ Legenda
okt 2015.
TechnoChrome ✌️
AMBASADOR→ Legenda
okt 2015.
savagestrain
AMBASADOR→ Legenda
420_DUDE
ENTUZIJASTA→ Poznavalac
okt 2015.
No Joke
ZMAJokt 2015.
savagestrain
AMBASADOR→ Legenda
okt 2015.
savagestrain
AMBASADOR→ Legenda
okt 2015.
Barbarossa
ZMAJokt 2015.
okt 2015.
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okt 2015.
okt 2015.