Answer:
Explanation:
You should allow the solvent to drop to the level of the adsorvent, so it would never run dry.
When you let your sample to run dry it will never finish to flow from the adsorbent depending of it polarity.
Water should not be used because it can dissolve the adsorbent.
You could use another technique to identify the compound, as an infrared or a ultraviolet detector. You can also, if you know the compounds, identify it for the retention time, for example, if you need to detect two compounds, one more polar than the other, and use a polar adsorbent and a non-polar solvent, the first compound to exit the column will be the less polar one, because it will have a bigger interaction with the solvent than the stationary phase (adsorbent) and will go faster, the second will be the more polar one, because it will have a bigger interaction with the stationary phase.
Total density of filled ball with nitrogen gas: 
The relationship between mass and volume can be easily determined using density; for example, the mass of a body is equal to its volume multiplied by the density (M = Vd), whereas the volume is equal to the mass divided by the density (V = M/d). The ball filled with nitrogen will not float in the air because total density of filled ball is greater than the density of an air. Density of the evacuated ball D = 0.214 g/L
Density of nitrogen gas = 
Mass of the nitrogen gas : 
Learn more about Mass and Density here:
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1. how does warming up help?
2. what does warming up do?
3. what would happen if you don’t warm up?
Answer:
263.1 is exactly three half-life, so the remaining portion is (1/2 x 1/2 x 1/2) of the original sample. That's 1/8 which is 12.5%
Ca^2+ and I^-
Na+ and Co3^2-
Ga^3+ and ClO3
Cu^2+ and F-
NH4^- and PO4^3-
Fe2+ and (SO4)^2-
Mg2+ and NO3^-
NH4^+ and NO2^-
K^+ and (C2H3O2)^- {C2H3O2 is acetate}
Na^+ and Cr2O7^2-
