It is hard because we can't get past the crust, Our machines will burn up at the mantle and so will we. The layers go: crust, mantle, outer core, inner core.
<span>The answer is 8. Hope this help!!!
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a) before addition of any KOH :
when we use the Ka equation & Ka = 4 x 10^-8 :
Ka = [H+]^2 / [ HCIO]
by substitution:
4 x 10^-8 = [H+]^2 / 0.21
[H+]^2 = (4 x 10^-8) * 0.21
= 8.4 x 10^-9
[H+] = √(8.4 x 10^-9)
= 9.2 x 10^-5 M
when PH = -㏒[H+]
PH = -㏒(9.2 x 10^-5)
= 4
b)After addition of 25 mL of KOH: this produces a buffer solution
So, we will use Henderson-Hasselbalch equation to get PH:
PH = Pka +㏒[Salt]/[acid]
first, we have to get moles of HCIO= molarity * volume
=0.21M * 0.05L
= 0.0105 moles
then, moles of KOH = molarity * volume
= 0.21 * 0.025
=0.00525 moles
∴moles HCIO remaining = 0.0105 - 0.00525 = 0.00525
and when the total volume is = 0.05 L + 0.025 L = 0.075 L
So the molarity of HCIO = moles HCIO remaining / total volume
= 0.00525 / 0.075
=0.07 M
and molarity of KCIO = moles KCIO / total volume
= 0.00525 / 0.075
= 0.07 M
and when Ka = 4 x 10^-8
∴Pka =-㏒Ka
= -㏒(4 x 10^-8)
= 7.4
by substitution in H-H equation:
PH = 7.4 + ㏒(0.07/0.07)
∴PH = 7.4
c) after addition of 35 mL of KOH:
we will use the H-H equation again as we have a buffer solution:
PH = Pka + ㏒[salt/acid]
first, we have to get moles HCIO = molarity * volume
= 0.21 M * 0.05L
= 0.0105 moles
then moles KOH = molarity * volume
= 0.22 M* 0.035 L
=0.0077 moles
∴ moles of HCIO remaining = 0.0105 - 0.0077= 8 x 10^-5
when the total volume = 0.05L + 0.035L = 0.085 L
∴ the molarity of HCIO = moles HCIO remaining / total volume
= 8 x 10^-5 / 0.085
= 9.4 x 10^-4 M
and the molarity of KCIO = moles KCIO / total volume
= 0.0077M / 0.085L
= 0.09 M
by substitution:
PH = 7.4 + ㏒( 0.09 /9.4 x 10^-4)
∴PH = 8.38
D)After addition of 50 mL:
from the above solutions, we can see that 0.0105 mol HCIO reacting with 0.0105 mol KOH to produce 0.0105 mol KCIO which dissolve in 0.1 L (0.5L+0.5L) of the solution.
the molarity of KCIO = moles KCIO / total volume
= 0.0105mol / 0.1 L
= 0.105 M
when Ka = KW / Kb
∴Kb = 1 x 10^-14 / 4 x 10^-8
= 2.5 x 10^-7
by using Kb expression:
Kb = [CIO-] [OH-] / [KCIO]
when [CIO-] =[OH-] so we can substitute by [OH-] instead of [CIO-]
Kb = [OH-]^2 / [KCIO]
2.5 x 10^-7 = [OH-]^2 /0.105
∴[OH-] = 0.00016 M
POH = -㏒[OH-]
∴POH = -㏒0.00016
= 3.8
∴PH = 14- POH
=14 - 3.8
PH = 10.2
e) after addition 60 mL of KOH:
when KOH neutralized all the HCIO so, to get the molarity of KOH solution
M1*V1= M2*V2
when M1 is the molarity of KOH solution
V1 is the total volume = 0.05 + 0.06 = 0.11 L
M2 = 0.21 M
V2 is the excess volume added of KOH = 0.01L
so by substitution:
M1 * 0.11L = 0.21*0.01L
∴M1 =0.02 M
∴[KOH] = [OH-] = 0.02 M
∴POH = -㏒[OH-]
= -㏒0.02
= 1.7
∴PH = 14- POH
= 14- 1.7
= 12.3
Answer:
Explanation:
Henry's law states that the solubility of a gas is directly proportional to its partial pressure. The equation may be written as:
Where 
is Henry's law constant.
Our strategy will be to identify the Henry's law constant for oxygen given the initial conditions and then use it to find the solubility at different conditions.
Given initially:
Also, at sea level, we have an atmospheric pressure of:
Given mole fraction:
According to Dalton's law of partial pressures, the partial pressure of oxygen is equal to the product of its mole fraction and the total pressure:
Then the equation becomes:
Solve for :
Now we're given that at an altitude of 12,000 ft, the atmospheric pressure is now:
Apply Henry's law using the constant we found:
