Answer:
The structures are attached in file.
Hydrogen bonding and intermolecular forces is the reason for ranks allotted.
Explanation:
In determining Lewis structure, we calculate the overall number of valence electrons available for bonding. Making carbon (the least electronegative atom) the central atom in the structure, we allocate valence electrons until each atom has achieved stability.
In order of decreasing affinity to water molecules:
This is due to the fact that the 
will accept protons more readily than the bicarbonate ion, 
. Carbonic acid, 
will not accept any more protons, hence it is the least attractive to water molecule, even though soluble.
Biphenyl will have a higher R value than the Methyl Orange.
Explanation:
Biphenyl is a aromatic hydrocarbon and it is a nonpolar molecule.
Methyl Orange is a organic compound with a -SO₃⁻Na⁺ polar functional group which will induce a high polarity in the compound.
You may find the chemical structures of both molecules in the attached picture.
Column chromatography, which use as stationary phase silica gel, is a good technique for separation of the Methyl Orange from Biphenyl.
Being a non-polar molecule, Biphenyl will have a higher R value than the Methyl Orange.
To separate them you use a appropriate solvent as eluent, as exemple chloroform, and Biphenyl will elute first from the column and after that, as a separate phase, Methyl Orange will elute thus separating them.
Learn more about:
chromatography
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Se2- has 34 protons and 36 electrons so it gets a 2- charge.
No, because the sun stays in the same exact place all of the time
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