Here's the other things from today.
- Pressure increases the solubility of gas in liquid. Increased pressure causes more gas particles to dissolve in the liquid, and decreased pressure allows more dissolved gas to escape from the liquid.
- Henry's law: The solubility of a gas in a liquid is directly proportional to the partial pressure of that gas on the surface of the liquid.
- The rapid escape of gas from a liquid in which it is dissolved is known as effervesence.
- Unlike a solid, increasing the temperature usually decreases gas solubility.
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ReplyDeleteI think the salt molecules' polarity gave it a stronger attraction to the water than the methanol, so because all the salt was taking up space near the water, the methanol was forced away
ReplyDeleteI think that the two most poler molecules, salt and water, came together while the less polar molecule of methanol went off away from the other two. Great video Jim.
ReplyDeleteI think in the first reaction the salt had a stronger attraction to the water leaving no "bonding" site for the methanol. In the second reaction the supersaturated liquid when more substance added the solid became more in quantity and absorbed the liquid. (my thoughts on the process)
ReplyDeletehttp://preparatorychemistry.com/Bishop_supersaturated.htm
ReplyDeleteGood site on supersaturated solutions
As for my theory, I believe the salt absorbs much of the water, therefore the methanol can no longer dissolve in the water.
i believe exactly what donnie said that because the salt absorbed the water, the methanol wasn't able to mix with the water and just sat on top
ReplyDeleteI believe that the salt bonds with water because salt is ionic and water is covalent.
ReplyDeleteI believe that the methanol does not have a strong attraction to water, and therefore was separated from it during the stirring process. The salt replaced it and the methanol rose to the top because it is less dense than water.
ReplyDeleteI think the salt took up the areas occupied by the methanol so that the salt water and methanol seperated.
ReplyDeletehttp://www.stevespanglerscience.com/experiment/00000078
ReplyDeleteHeres a good site on supersaturated solutions
here is a website talking about the sodium acetate demonstration. and i think they didnt mix because of the nonpolar and polar ends on each of the three substances.
ReplyDeletehttp://www.instructables.com/id/Crystallization-of-homemade-sodium-acetate/
I think that the water had the correct number of orbitals to bond with the salt.
ReplyDeletegood website on henry's law.
ReplyDeletehttp://dwb.unl.edu/Teacher/NSF/C09/C09Links/www.chem.ualberta.ca/courses/plambeck/p101/p01182.htm
here's a good video on effervescence:
ReplyDeletehttp://www.metacafe.com/watch/1550867/effervescence/
And i think the attraction between the salt and the water forced them together while the methanol was less dense and not attracted to it.
http://www.protocol-online.org/biology-forums/posts/24672.html
ReplyDeletehey guys this is a good site about concentration protocol in lab settings and such