We know that is aqueous solution the following equilibrium operates......
H_2O(l) rightleftharpoonsH^(+) + HO^-H2O(l)⇌H++HO−
H^+H+ and HO^-HO− are the characteristic cation, and characteristic anion of the water solvent. Sometimes, we write H^+H+ as H_3O^+H3O+, i.e. the "hydronium ion"hydronium ion. As far as anyone knows this is a cluster of 3-4 (or more) water molecules, with an extra PROTON, H^+H+ to give H_7O_3^+H7O+3, or H_9O_4^+H9O+4, we use H^+H+ and H_3O^+H3O+ as convenient shorthands.
As with any equilibrium we can quantify it......
K=([H^+][HO^-])/[[H_2O(l)]]K=[H+][HO−][H2O(l)]
Because [H_2O][H2O] is so large, it can be removed from the equation, and we get
K_w=[H^+][HO^-]=[H_3O^+][HO^-]=10^(-14)Kw=[H+][HO−]=[H3O+][HO−]=10−14 at 298*K298⋅K. Now back in the day before the advent of electronic calculators, scientists used log tables to the "base e"base e or "base 10"base 10 to simplify products and quotients of very large and very small numbers.
We DEFINE pH=-log_10[H_3O^+]pH=−log10[H3O+], and pOH=-log_10[HO^-]pOH=−log10[HO−], and thus if we take log_10log10 of
K_w=[H^+][HO^-]=[H_3O^+][HO^-]=10^(-14)Kw=[H+][HO−]=[H3O+][HO−]=10−14.....
..............we gets.................
log_10K_w=log_10[H_3O^+]+log_10[HO^-]=log_10(10^-14)log10Kw=log10[H3O+]+log10[HO−]=log10(10−14)
And on rearrangement,
-14=log_10[H_3O^+]+log_10[HO^-]−14=log10[H3O+]+log10[HO−], and multiplying thru by -1−1..
14=underbrace(-log_10[H_3O^+])_(pH)underbrace(-log_10[HO^-])_(pOH)
And finally our defining relationship......pH+pOH=14. Wheww!
And so we can at last address your question. I will do the first row in the table. I suggest that you have a go at the rest yourself.
"Solution A", [H^+]=3.7xx10^-8*mol*L^-1; pH=-log_10(3.7xx10^-8)=7.43; pOH=14-7.43=6.57. And [HO^-]=10^(-6.57)=2.70xx10^-7*mol*L^-1.
Over to you for B and C and D hoss............
One final caveat: I stress that H^+ is equivalent to H_3O^+; which expression you use is a matter of personal preference, but be consistent.