#OC
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<@&1227988359910260737>
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benzaldehyde
not acc to key
it somehow does benzoin condensation
without ethanol
huh
KCN hmmm
but then there is nothing else in the solution
how
do they make anything except a cyanohydrin
but your thing mentioned "neat KCN"
fr
what is O
benzene
What the hell is ZnCl3?
idk either
Salt
Zn3+?
ZnCl2 is a weak lewis acid catalyst, similar to the ones we use in Fredielcraft reactions
Like AlCl3
if I had to guess, I would say the mechanism is very similar to acylation.
Instead of ending up with a carbonyl cation, you should get H3C - C(+) =N which can substitute into the benzene ring
looks probable. The catalysts are very similar to acylation reaction's.
Ag and heat just precipitates out white AgI from the CH3-I
So you have acetylene formed from that step, which undergoes cyclisation and aromatisation
to O
HCl and HgCl2 can hydrate actylene to form acetaldehyde, kucherov reaction.
and again, cyanohydrin formation in G to K
@kindred berry does this make sense
its ZnCl3 tho
Why isnt this forming vinyl chloride which goes polymerisation to make PVC
i found some
weird named
condensation
which can have Zn salt to be used as catalyst
@sudden badger @kindred berry @slender rose @manic gull
knovangle?
knovangle
angel
language
sorry
Kya hua boss? 🙃
meine jo knoevenagel padhi hai usmein amine ya pyridine use hota hai
we good? @kindred berry
Yeag
+faolved @slender rose
+fsolved @slender rose
