A saturated solution is one in which no more solute is able to dissolve in a given solvent at a particular temperature. Some amount of the solute is left undissolved in the solution.
Unsaturated solution has solute in lower proportions than required to form a saturated solution.
Supersaturated solution has solute in amounts greater than a saturated solution.
We can take the help of solubility curve in order to find out the amount of a salt required to prepare a saturated solution of that salt at a particular temperature.
The solubility of KI at 10
is 136 g/ 100 mL water
The solubility of 
at 
is 21 g/100 mL water.
The solubility of 
at is 80 g/100 mL water.
The solubility of NaCl at is 38 g/ 100 mL water.
So the correct answer will be KI, as it would need 136 g KI / 100 mL water to form a saturated solution at .So, if we have 80g KI/ 100mL water it would be an unsaturated solution.
C12H22O11 aka carbon, hydrogen, and oxygen
600,000 mm if im not mistaken.
Answer:
Swelling of the red blood cells occurs.
Explanation:
- <u>Distilled water makes the blood hypotonic ,. that is a less concentrated solution, to the body tissues including the red blood cells. </u>
- Therefore the water will enter the red blood cells and may cause them to lyse or swell.
- <em>Additionally , water will enter the tissue spaces and cause sweling. </em>
- But in the case of a hypertonic solution , ( a salt or saline solution ) , <em>This swelling does not happen because the concentration of the saline will be equal or more than the blood. </em>
- Thus the water will flow only from the blood to the solution. <u>This will not cause swelling.</u>
- But too much of salt is also not recommended.
Nonane (b) has the highest melting point.
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A caveat: I'm assuming that we're dealing with the straight-chain isomers of these alkanes (specifically pentane and nonane). The straight-chain isomer of pentane (<em>n</em>-pentane, CH3-[CH2]3-CH3) has a melting point of -129.8 °C; the straight-chain isomer of nonane (<em>n-</em>nonane, CH3-[CH2]7-CH3) has a melting point of -53.5 °C. The pattern holds as you go down (or up): The more carbon atoms, the higher the melting point. So, in decreasing order of melting points here, you'd have the following: nonane > pentane > butane > ethane.
However, one structural isomer of pentane, neopentane, has a melting point of -16.4 °C, which is <em>higher </em>that the melting point of <em>n</em>-nonane despite neopentane having the same molecular formula as its straight-chain isomer. Of course, you're not to blame for coming up with this question; this is just some extra info to keep in mind.
