What is the pH of a solution that is 0.62M H2SO4(aq) and 1.7M HCOOH (formic acid).

This is a VERY complicated problem but here goes.

H2SO4 is a strong acid for the first H that ionizes but a relatively weak acid for the second H. HCOOH is a weak acid.
First, determine the H^+ from H2SO4.
H2SO4 ==> H^+ + HSO4^-
HSO4^- ==> H^+ + SO4^2-
k2 for HSO4^- is (H^+)(SO4^-)/(HSO4^-).
Substitute into k2. For H^+ you substitute 0.62+x. For SO4^2- you substitute x and for (HSO4^-) you substitute 0.62-x. Solve the quadratic for x, then obtain 0.62+x and that will give you the H^+ from the H2SO4. If I didn't make a mistake you should get about 0.08M.
Then HCOOH is a weak acid and it ionizes as
HCOOH ==> H^+ + HCOO^-
Set up an ICE chart and look up Ka for HCOOH. The H^+ will be decreased by Le Chatelier's Principle (due to the H^+ from H2SO4). Substitute H^+ from H2SO4 for H^+ an solve for HCOO^-. Then add
H^+ from H2SO4 + H^+ from HCOOH to find the total H^+ and divide by liters soln to find M. Convert to pH.

To determine the pH of a solution containing both H2SO4 and HCOOH, we need to consider the individual contributions of each acid to the total concentration of H+ ions.

First, let's determine the concentration of H+ ions from H2SO4:
H2SO4 dissociates completely into two H+ ions and one SO4^-2 ion.
Therefore, the concentration of H+ ions from H2SO4 is equal to the molarity of H2SO4, which is 0.62 M.

Next, we need to consider the contribution of H+ ions from HCOOH:
HCOOH partially dissociates into one H+ ion and one HCOO^- ion.
The extent of dissociation, or ionization, depends on the acid's dissociation constant (Ka) and the initial concentration of HCOOH.
Let's assume the ionization of HCOOH is x. Therefore, for every x moles that ionize, we have x moles of H+ ions.

The dissociation reaction of HCOOH can be represented as follows:
HCOOH ⇌ H+ + HCOO^-

Using the given concentration of HCOOH (1.7 M), we can express the equilibrium expression for the ionization of HCOOH as:
Ka = [H+][HCOO^-] / [HCOOH]

Since the concentration of H+ ions is equal to x and the concentration of HCOOH is equal to (1.7 - x) due to the ionization, we can write the equation as:
Ka = x * (1.7 - x) / (1.7 - x)

Given that the Ka value for formic acid is 1.8 x 10^-4, we can solve this quadratic equation to find the value of x. However, for simplicity, we can make an approximation that x is negligible compared to 1.7, which is reasonably accurate for highly dilute solutions.

Considering that the x value is relatively small, we can ignore it in the denominator of the equation when calculating the concentration of H+ ions. In that case, we can calculate the concentration of H+ ions from HCOOH as the initial concentration of HCOOH, which is 1.7 M.

Now, we can determine the total concentration of H+ ions in the solution. Since the H+ ions from H2SO4 and HCOOH are present together, we can simply add the individual concentrations:
Total concentration of H+ ions = Concentration of H+ ions from H2SO4 + Concentration of H+ ions from HCOOH
Total concentration of H+ ions = 0.62 M + 1.7 M

Finally, to calculate the pH, we use the equation:
pH = -log[H+]

Substituting the total concentration of H+ ions into this equation, we can find the pH value.