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
Answer:
See explaination
Explanation:
please kindly see attachment for the step by step solution of the given problem.
<span>Answer:
Graham's law of gaseous effusion states that the rate of effusion goes by the inverse root of the gas' molar mass.
râšM = constant
Therefore for two gases the ratio rates is given by:
r1 / r2 = âš(M2 / M1)
For Cl2 and F2:
r(Cl2) / r(F2) = âš{(37.9968)/(70.906)}
= 0.732 (to 3.s.f.)</span>
Answer:
124.91mL
Explanation:
Given parameters:
P₁ = 1.08atm
V₁ = 250mL
T₁ = 24°C
P₂ = 2.25atm
T₂ = 37.2°C
V₂ = ?
Solution:
To solve this problem, we are going to apply the combined gas law;

P, V and T represents pressure, volume and temperature
1 and 2 delineates initial and final states
Convert the temperature to kelvin;
T₁ = 24°C, T₁ = 24 + 273 = 297K
T₂ = 37.2°C , T₂ = 37.2 + 273 = 310.2K
Input the variables and solve for V₂

V₂ = 124.91mL
Answer:

Explanation:
Hello there!
In this case, given the neutralization of the acetic acid as a weak one with sodium hydroxide as a strong base, we can see how the moles of the both of them are the same at the equivalence point; thus, it is possible to write:

Thus, we solve for the molarity of the acid to obtain:

Regards!