Solving Solubility Doubt: Sodium Benzoate vs. Toluene

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SUMMARY

Sodium benzoate is more soluble in water than in toluene, as confirmed by the discussion. The ionic nature of sodium benzoate contributes to its high solubility in polar solvents like water. While sodium benzoate shares an aromatic nucleus with toluene, which suggests potential solubility, the polar interactions in water significantly enhance its solubility compared to toluene. Computational chemistry is necessary to analyze solubility limits for complex compounds.

PREREQUISITES
  • Understanding of ionic compounds and their solubility in polar solvents
  • Knowledge of molecular interactions, particularly between polar and non-polar substances
  • Familiarity with the concept of aromatic compounds
  • Basic principles of computational chemistry
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  • Research the solubility rules for ionic compounds in various solvents
  • Learn about molecular interactions, focusing on polar vs. non-polar interactions
  • Study the properties of aromatic compounds and their behavior in different solvents
  • Explore computational chemistry techniques for predicting solubility
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Chemistry students, researchers in solubility studies, and professionals in chemical engineering or materials science will benefit from this discussion.

jaumzaum
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I was solving an exercise where I had to judge (true or false) 5 statements. One of them said:

"Sodium benzoate is more soluble in water than in toluene"

The book answer is true, but I don't know how to compare it.

I mean, sodium benzoate is ionic, and water is very polar, so the solubility of the salt in water should be great. Nevertheless sodium benzoate has a aromatic nucleus, that is the same of toluene, so they should share pretty much the same molecular interactions and one should reasonably dissolve another too. Am I thinking wrong? If not, how should I compare both of the solubilities?

Thanks
John
 
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Nope you're thinking too hard. If it is ionic in general it is soluble in polar solvents.

Now there is a cutoff. A 500000 dalton hydrocarbon polymer with a single charged group is obviously not going to be soluble. Where is the cutoff? Hard to say.

That requires computational chemistry.
 

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