Answer:
the first energy level is closest to nuclear the second energy level is a little farther away than the first
When we can get Pka for K2HPO4 =6.86 so we can determine the Ka :
when Pka = - ㏒ Ka
6.86 = -㏒ Ka
∴Ka = 1.38 x 10^-7
by using ICE table:
H2PO4- → H+ + HPO4
initial 0.4 m 0 0
change -X +X +X
Equ (0.4-X) X X
when Ka = [H+][HPO4] / [H2PO4-]
by substitution:
1.38 X 10^-7 = X^2 / (0.4-X) by solving for X
∴X = 2.3x 10^-4
∴[H+] = X = 2.3 x 10^-4
∴PH = -㏒[H+]
= -㏒ (2.3 x 10^-4)
∴PH = 3.6
The answer to this question is a
Answer:
9.4
Explanation:
The equation for the reaction can be represented as:
+
⇄ 
The ICE table can be represented as:
+
⇄ 
Initial 0.27 0.49 0.0
Change -x -2x x
Equilibrium 0.27 - x 0.49 -2x x
We can now say that the concentration of
at equilibrium is x;
Let's not forget that at equilibrium
= 0.11 M
So:
x = [
] = 0.11 M
[
] = 0.27 - x
[
] = 0.27 - 0.11
[
] = 0.16 M
[
] = (0.49 - 2x)
[
] = (0.49 - 2(0.11))
[
] = 0.49 - 0.22
[
] = 0.27 M
![K_C = \frac{[CH_3OH]}{[CO][H_2]^2}](https://tex.z-dn.net/?f=K_C%20%3D%20%5Cfrac%7B%5BCH_3OH%5D%7D%7B%5BCO%5D%5BH_2%5D%5E2%7D)


= 9.4
∴ The equilibrium constant at that temperature = 9.4
Answer:
+2
Explanation:
If a compound
existed, we would identify the oxidation state of sulfur using the following logic:
- oxygen is more electronegative than sulfur, so it's more electron-withdrawing and it should have a negative oxidation state producing a positive oxidation state for sulfur;
- oxygen typically has an oxidation state of -2;
- we may then apply the fact that SO is expected to be a molecule with a net charge of 0;
- if the net charge is 0 and the oxidation state of oxygen is -2, we may set the oxidation state of S to x;
- write the equation for the net charge of 0 by adding all individual charges of the two atoms:
; - hence, x = 2.
That said, in this hypothetical compound S would have an oxidation state of +2.