Unanswered Questions
689 questions with no upvoted or accepted answers
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Is there a reliable chemical theory that predicts pKa based on structure?
Obviously, there are general stability arguments that can be made to estimate relative pKas, such as evaluating the stability of the conjugate base of an acid, or thinking about how polarized the bond ...
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Order of Basicity of Nitrogen Trihalides
I was asked to arrange nitrogen tri-halides in order of increasing basicity. On looking up the answer online, it turned out to be the following: $\ce{NF3}$ < $\ce{NCl3}$ < $\ce{NBr3}$ < $\ce{...
CommunityBot
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Why is o-fluorophenol a stronger acid than p-fluorophenol?
The $\mathrm{p}K_\mathrm{a}$ value of o-fluorophenol is $8.7$, while that of the p-fluorophenol is $9.9$. It's obvious that the inductive effect is more dominant at ortho-position, which results in a ...
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Steric inhibition of resonance vs. hydrogen bonding
I have to compare the acidic strength of these compounds:
Now, in A and B hydrogen bonding will be present which will help stabilize the negative charge of the conjugate base. However, the hydroxyl ...
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Does phosphoric acid remove stainless steel electropolished layer?
Electropolished stainless steel has a high corrosion resistance due to the oxide film that is created during electropolishing. The film mainly consist of chromium(III) oxide.
Phosphoric acid is ...
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Ligand strength - Coulombic effect and/or Electronegativities?
According to my teacher, these three Lewis bases generally decrease in strength in the following order:
Ammonia
Water
Hydroxide ion
I agree. However, he argues that their ability to act as Lewis ...
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Why is carbon monoxide non-Brönsted-basic in aqueous solution when it has a lone pair on carbon?
Carbon monoxide is not protonatable in aqueous solution; a quick Google search even leads to a paper that talks about using carborane acids, i.e. extreme superacids, to protonate the molecule.
However,...
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Why is supersaturated sodium acetate so (meta)stable?
Sodium acetate is a common example used in general chemistry lectures to illustrate the idea of supersaturation, and that precipitation of a supersaturated solution can be initiated by a seed crystal. ...
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pKa of different sites of butanone
From what I can tell, deprotonation of the central hydrogen leads to the more thermodynamically stable product (most substituted double bond. i.e. most stabilization by hyperconjugation). Therefore, ...
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How can copper(II) sulfate crystallize outside a glass vial?
I'm making copper sulfate crystals in glasses. Within a few weeks, the copper sulfate seems to crystallize both inside and outside the glass:
(A few weeks after making a new solution)
(Yet another ...
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How does a 5th hydrogen bind to carbon atom in CH5[+]?
Can we bind a fifth hydrogen to a carbon atom if carbon is not in excited state?
We have a big discussion in class and cannot clearly answer the question. If carbon atom excites an electron from $2\...
- 17.4k
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Yellow precipitate in SnCl2 solution
I have a few small bottles of 0.5M $\ce{SnCl2}$ solution, however solution was prepared about 4 months ago, and there is a yellow precipitate on the bottom of each bottle. Working hypothesis is that ...
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What is the pKa of the O-17 hydronium ion?
At low concentrations of a conjugate acid/base pair in aqueous solutions, the Henderson-Hasselbalch equation gives a good approximation of the ratio of acid and base:
$$ \frac{[\ce{A-}]}{[\ce{AH}]} = ...
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Comparing acidic strength of phthalic acid isomers
I'd like to compare the acidic strengths of phthalic, isophthalic and terephthalic acids. As I understand, phthalic acid is the most acidic due to steric inhibition of resonance (SIR), but as ...
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What pH value of 1M sodium crotonate solution supposed to be?
I need to prepare the $\pu{1M}$ solution of sodium crotonate, however, I don't have one in lab, but I do have sodium hydroxide and crotonic acid.
Thus, I calculated that for $\pu{100 mL}$ of $\pu{1M}$ ...
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