At equilibrium the concentrations of:
[HSO₄⁻] = 0.10 M;
[SO₄²⁻] = 0.037 M;
[H⁺] = 0.037 M;
There is initially very little H+ and no SO₄²⁻ in the solution. A salt is KHSO₄⁻. All KHSO₄⁻ will split apart into K⁺ and HSO₄⁻ ions. [HSO₄⁻] will initially be present at a concentration of 0.14 M.
HSO₄⁻ will not gain H⁺ to produce H₂SO₄ since H₂SO₄ is a strong acid. HSO₄⁻ may act as an acid and lose H⁺ to form SO₄²⁻. Let the final H⁺ concentration be x M. Construct a RICE table for the dissociation of HSO₄²⁻.
R
⇄ 
I 
C

E

×
for
. As a result,
![\frac{[H^+]. [SO_4^2^-]}{HSO_4^-} = K_a](https://tex.z-dn.net/?f=%5Cfrac%7B%5BH%5E%2B%5D.%20%5BSO_4%5E2%5E-%5D%7D%7BHSO_4%5E-%7D%20%3D%20K_a)
is large. It is no longer valid to approximate that
at equilibrium is the same as its initial value.

×
× 
Solving the quadratic equation for
since
represents a concentration;

Then, round the results to 2 significant figure;
Learn more about concentration here:
brainly.com/question/14469428
#SPJ4
Q. Which type of radioactive decay can pass through the body?
A. Gamma Rays
So the ideal gas law is pv=nrt
The letter n stands for the number of moles. divide both side by rt to isolate.
pv/rt=n
Answer:
use google and use the first link
Explanation:
C5H12 (l) + 8O2 (g) ----> 5CO2 (g) + 6H2O (l)
Delta H = -3505.8 kJ/mol
C (s) + O2 (g) -----> CO2 (g)
Delta H = -393.5 kJ/mol
H2 (g) + (1/2)O2 (g) ------> H2O (l)
Delta H = -286 kJ/mol
Possible answers:
a. +35 kJ/mol
b. + 1,073 kJ/mol
c. -4,185 kJ/mol
d. -2,826 kJ/mol
e. -178 kJ/mol