All Questions
10
questions
1
vote
0
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56
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Quenching reagents for specific reaction
A reaction general procedure is given as follows:
A mixture of 2-fluoro-5-iodo pyridine $(\pu{1.0 mmol})$, methyl
acetoacetate $(\pu{3.0 mmol})$, $\ce{CuI}$ $(\pu{10 mol\%})$, $\ce{K3PO4}$ $(\pu{3.0 ...
2
votes
1
answer
155
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Can antimony pentafluoride be made by adding hydrogen fluoride to antimony trifluoride?
I was looking at how the strongest acid was made and I found something I did not understand. On the Wikipedia page for antimony trifluoride it shows the production of $\ce{SbF3}$ using $\ce{HF}$:
$$\...
4
votes
1
answer
2k
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Net ionic equation for a synthesis reaction?
In the following reaction
$$\ce{S (s) + O2 (g) -> SO2 (g)}$$
there are no spectator ions because both $\ce{S}$ and $\ce{O2}$ take part in the reaction. Does that mean the net ionic equation is ...
10
votes
1
answer
2k
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Reaction mechanism for the synthesis of 9,10-phenanthrenequinone
In my lab course I had to synthesize 9,10-phenanthrenequinone (phenanthrene-9,10-dione) from phenanthrene and chromium(VI) oxide. The synthesis was made as explained in Organic Syntheses, Coll. Vol. 4,...
1
vote
0
answers
54
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Polymer synthesis with redox initiation
I made four different samples of poly acrylic nitrile (PAN) by going through a precipitation polymerization. The system was initiiated by the redox system $\ce{K2S2O8}$, $\ce{FeSO4}$ and $\ce{Na2S2O5}$...
0
votes
0
answers
407
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Production of fluorine gas
I have to suggest a method in order to produce $\ce{F2}$. It also says that I should consult the redox potential values. I know that there is a way to produce fluoride which is:
$$\ce{K2[MnF6] + 2 ...
14
votes
1
answer
2k
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What are the practical differences between the various DMSO oxidations (Swern, etc.)?
Recently, I was reading a paper about a total synthesis of (+)-rubriflordilactone A (the article is open access: Angew. Chem. Int. Ed. 2015, 54 (43), 12618–12621). In two different steps where an ...
6
votes
2
answers
584
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Side chain hydroxylation of pyrrole
What reagents are required to form 1-[1,5-dimethyl-3-phenyl-4-(propan-2-yl)-1H-pyrrol-2-yl]propan-1-ol with 1,2-dimethyl-4-phenyl-3-(propan-2-yl)-5-propyl-1H-pyrrole as starting material?
Is it ...
3
votes
2
answers
13k
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What is this brown liquid that I got when I boiled glycerol and water solution?
I boiled a solution of glycerol and water at about 160 degree Celsius and got a brown liquid much less in volume (boiled off the entire water I think; also not so sure about the accurate temperature). ...
10
votes
1
answer
2k
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Oxidative chlorination mechanism (sulfide to sulfonyl chloride)
I cannot find much guidance in the literature. Any ideas as to what the mechanism of this reaction might be?