Cou
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Are hexane and petroleum ether interchangeable?
a common introductory grignard reaction lab is preparation of triphenylmethanol with bromobenzene. THe coupling side product is biphenyl, which is
removed with petroleum ether.
petroleum ether is mainly a mixture of aliphatic pentanes and hexanes. I already have hexane, can't I use that? Is there any reason why lab procedures
want you to use petroleum ether instead?
edit: i found a procedure that uses hexane to extract biphenyl http://web.mst.edu/~tbone/Subjects/TBone/chem228/grignard.pd...
[Edited on 11-19-2020 by Cou]
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DraconicAcid
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Petroleum ether is a mixture, and is generally cheaper. That's about it.
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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Cou
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Weird, because the amazon listings for hexane are cheaper than petroleum ether.
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woelen
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Where I live, hexane also is cheaper. Pentane is more expensive. If I want to buy n-hexane, then I pay a premium price, but simply buying hexane (mix
of isomers) is dirt-cheap.
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Fyndium
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How useful are hexanes, pet ether and similar hydrocarbons in biphasic extractions compared to toluene? They boil lower and are immiscible with water,
but do they have similar solvent properties?
They used barrels of gasoline as a solvent in a documentary regarding Colombian's most important export goods, so it must not be too terrible?
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chemship1978
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It's cheap, that's why. It also depends on the solute itself. If you could narrow down the group of compounds to dissolve, maybe we could come up with
an answer?
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Fery
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Whenever possible I use medicinal petrolether, I've bought 10 L barrel of it not more than 1 year ago. It is very cheap in my country (10 L for circa
40 EUR) and it is always hydrogenated so no alkenes present. Sometimes I redistill it through column when I need some fractions boiling at some
temperature range (when using it in Dean-Stark trap apparatus so later I can separate the petrolether fraction from the dehydrated organic compound by
distillation). For extractions no need to bother to redistill its fractions. I have also pure n-pentane, n-hexane, n-heptane (circa 20 EUR per 1 L
bottle of each one) but medicinal petrolether was most of times OK for me and it was circa 5 times cheaper.
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Deathunter88
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Don't buy solvents on Amazon, period. Overpriced and not representative of true prices. Coleman fuel is petroleum ether, might be worth distilling
first though.
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DraconicAcid
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Quote: Originally posted by Fyndium  | How useful are hexanes, pet ether and similar hydrocarbons in biphasic extractions compared to toluene? They boil lower and are immiscible with water,
but do they have similar solvent properties?
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Toluene is a pretty good solvent for a lot of things- petroleum ether and similar hydrocarbons are poor solvents for anything that's not completely
non-polar.
I say this based on the number of things that I've recrystallized from toluene by adding petroleum ether as an anti-solvent.
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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Cou
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For example, salicylic acid is soluble in toluene, but not in hexane.
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Fyndium
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I see. There is a reason why hexane and pet's aren't used as solvents in any synthesis writeups despite their low cost and ease of availability.
Good thing I just purified a lot of toluene from a canister of paint thinner.
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Texium
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Hexanes or petroleum ether is most commonly used for column chromatography, where it would be paired with a more polar solvent such as DCM or ethyl
acetate to make a mixture tuned to effectively separate whatever mixture you have on hand. Other than that, it's a great degreaser!
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DraconicAcid
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Also, it's useful as an antisolvent because of its low boiling point. Use it to wash your precipitate, and it dries quickly. Put a test tube of a
solution in a larger container of pentane, and let the crystals grow by vapour diffusion.
From experience, I know that piperine, benzoic acid, and triphenylmethanol are almost completely insoluble in pet ether. Substituted arene metal
carbonyl complexes (such as RC6H5-Cr(CO)3, for example) *are* soluble in light hydrocarbon solvents.
Please remember: "Filtrate" is not a verb.
Write up your lab reports the way your instructor wants them, not the way your ex-instructor wants them.
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AvBaeyer
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To answer the original question, hexanes can almost always replace petroleum ether. The only time this can become a problem is when the low boiling
pet ether is used for crystallization of low melting compounds. Switching to hexanes or higher boiling pet ether fractions will often result in
"oiling out" of the product.
Years ago various hydrocarbon solvents were sold under the "Skellysolve" name and maybe still are. Here is some information regarding these solvents
some of which are referred to as petroleum ether. I cannot remember where I originally found this information.
Skellysolve –Petroleum ether solvents
A: Essentially n-pentane, bp 28-30
B. Essentially n-hexane, bp 60-68
C. Essentially n-heptane, bp 90-100
D. Mixed heptanes, bp 75-115
E. Mixed octanes, bp 100-140
F. Petroleum ether, bp 30-60
G. Petroleum ether, bp 40-75
H. Mix of hexanes and heptanes, bp 69-96
L. Essentially octanes, bp 95-127
Purification method.
Shake several times with conc. H2SO4, then 10% H2SO4 and conc KMnO4 until permanganate color persists. This removes unsaturated and aromatic
hydrocarbons. Wash with water, sodium carbonate then water. Dry over CaCl2 or Na2SO4 and distill. Filter through activated alumina to remove epoxides.
Simple distillation of Coleman fuel will provide the fractions listed above, especially E - L. I have done this several times.
Hope this is useful.
AvB
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macckone
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There is a video of a similar procedure with gasoline on extractions & ire channel.
https://www.youtube.com/watch?v=FP5JaSH4ysA
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