The correct answer is B) Chlorine, Sulfur, and Silicon
I'm 100% sure this is correct
Brainliest please!!!
Answer:
pH = 3.3
Explanation:
Buffer solutions minimize changes in pH when quantities of acid or base are added into the mix. The typical buffer composition is a weak electrolyte (wk acid or weak base) plus the salt of the weak electrolyte. On addition of acid or base to the buffer solution, the solution chemistry functions to remove the acid or base by reacting with the components of the buffer to shift the equilibrium of the weak electrolyte left or right to remove the excess hydronium ions or hydroxide ions is a way that results in very little change in pH of the system. One should note that buffer solutions do not prevent changes in pH but minimize changes in pH. If enough acid or base is added the buffer chemistry can be destroyed.
In this problem, the weak electrolyte is HNO₂(aq) and the salt is KNO₂(aq). In equation, the buffer solution is 0.55M HNO₂ ⇄ H⁺ + 0.75M KNO₂⁻ . The potassium ion is a spectator ion and does not enter into determination of the pH of the solution. The object is to determine the hydronium ion concentration (H⁺) and apply to the expression pH = -log[H⁺].
Solution using the I.C.E. table:
HNO₂ ⇄ H⁺ + KNO₂⁻
C(i) 0.55M 0M 0.75M
ΔC -x +x +x
C(eq) 0.55M - x x 0.75M + x b/c [HNO₂] / Ka > 100, the x can be
dropped giving ...
≅0.55M x ≅0.75M
Ka = [H⁺][NO₂⁻]/[HNO₂] => [H⁺] = Ka · [HNO₂]/[NO₂⁻]
=> [H⁺] = 6.80x010⁻⁴(0.55) / (0.75) = 4.99 x 10⁻⁴M
pH = -log[H⁺] = -log(4.99 x 10⁻⁴) -(-3.3) = 3.3
Solution using the Henderson-Hasselbalch Equation:
pH = pKa + log[Base]/[Acid] = -log(Ka) + log[Base]/[Acid]
= -log(6.8 x 10⁻⁴) + log[(0.75M)/(0.55M)]
= -(-3.17) + 0.14 = 3.17 + 0.14 = 3.31 ≅ 3.3
Answer:
a) 
b) 
Explanation:
Equation of reaction:
Initial pressure 3 1 0
Pressure change 2P 1P 2P
Total pressure = (3-2P) + (1-P) + (2P)
Total Pressure = 3.75 atm
(3-2P) + (1-P) + (2P) = 3.75
4 - P = 3.75
P = 4 - 3.75
P = 0.25 atm
Let us calculate the pressure of each of the components of the reaction:
Pressure of XO2 = 3 - 2P = 3 - 2(0.25)
Pressure of XO2 =2.5 atm
Pressure of O2 = 1 - P = 1 -0.25
Pressure of O2 = 0.75 atm
Pressure of XO3 = 2P = 2 * 0.25
Pressure of XO3 = 0.5 atm
From the reaction, equilibrium constant can be calculated using the formula:
![K_{p} = \frac{[PXO_{3}] ^{2} }{[PXO_{2}] ^{2}[PO_{2}] }](https://tex.z-dn.net/?f=K_%7Bp%7D%20%3D%20%5Cfrac%7B%5BPXO_%7B3%7D%5D%20%5E%7B2%7D%20%7D%7B%5BPXO_%7B2%7D%5D%20%5E%7B2%7D%5BPO_%7B2%7D%5D%20%7D)
Standard free energy:
b) value of k−1 at 27 °C, i.e. 300K
