@Will what do you mean when you write 'what properties of a gaseous chemical would facilitate the fastest evaporation'? That doesn't really seem to go together. (And please don't use edit statements, make it standalone; if anyone were interested in how it came about, it's in the edit history.)
@Martin-マーチン Go together with what? Allowing water to evaporate into/among some gas X will lead to different phenomena/results depending on what species of gas X is used (e.g., air VS SF6). I'm looking for whatever gas will facilitate evaporation the most/fastest. Doesn't seem like a hard to understand question to me... although I admit it might be hard to answer?
I was working through the end-of-chapter exercises of the acid-base chapter in Shriver's Inorganic Chemistry when I came across the following problem:
4.7. The effective proton affinity $\ce{A^{'}_{p}}$ of $\ce{F-}$ in water is 1150 kJ $\ce{mol^-}$. Predict whether it will behave as an acid o...
@Will If you're that defensive about it, then I am very sorry, but I cannot help you. The way you have formulated the question here makes it much more understandable though. The parameters you set (basically none) makes this question a bit broad, just like it was stated previously.
Simple prefixes (simple substituent groups such as methyl and isopropyl) are arranged alphabetically disregarding any multiplicative prefixes. Any multiplicative prefixes are inserted later and do not alter the alphabetical order.
For example, ‘methyl’ is considered to begin with ‘m’; ‘isopropyl’...
I've been playing around with ChemDraw and found that it assigns the priorities of substituents in a way I wouldn't have expected, depending on the length of the alkyl substituent. I'm not a nomenclature buff, so I'd like to know if it's correct and if so, why.
$n = 1$: 1-ethyl-2-iodobenzene
...
I'm voting to close this question as off-topic because it is not about physics. Try the Gruesome Methods of Execution Stack Exchange. — John Rennie17 mins ago
Last night dream. Three strange nonexistent chemical reactions:
2
(and yes, that is some kind of pendant pentane)
(This one is even bizarre when you consider how it is described in the dream: After the double bond is broken, 2 carbon bonds wander in space leading to switching in positions of 5 and 6 membered rings)
(This one I think it has the largest chance to have a real life counterpart. Basically, the scheme is showing some kind of biomolecular capsule that is easily synthesized, which can be cleaved in a chemoselective fashion to give the pure product as shown (modulo some oxygen side groups I forgot where they were)
(also forgot to say that the -1,2(forgot) thing is triggered when two such heteronuclear double bonds are at close proximity and juxapositioned like as if they are going to undergo metathesis)
I was working through the end-of-chapter exercises of the acid-base chapter in Shriver's Inorganic Chemistry when I came across the following problem:
4.7. The effective proton affinity $\ce{A^{'}_{p}}$ of $\ce{F-}$ in water is 1150 kJ $\ce{mol^-}$. Predict whether it will behave as an acid o...
If the energy less than the work function is phton ejection of
I've been playing around with ChemDraw and found that it assigns the priorities of substituents in a way I wouldn't have expected, depending on the length of the alkyl substituent. I'm not a nomenclature buff, so I'd like to know if it's correct and if so, why.
$n = 1$: 1-ethyl-2-iodobenzene
...
The Periodic Table
The Periodic Table