SrSo4 = Sr(2+) + SO4(2-)
Let’s say that the initial concentration of SrSo4 was 1. ( or we have 1 mole of this reagent).
When The reaction occurs part of SrSo4is dissociated. And we get X mole Sr(2+) and So4(2-).
Ksp=[Sr(2+)]*[SO4(2-)]
X^2=3.2*10^-7
X=5.6*10^-4
Answer:
Explanation:
2. You work for an environmental company as an environmental toxicologist and have been hired to determine the contaminant present in a local resident’s pool. Create a flow chart outlining how you would detect the possible presence of Fe2+ and/or Sr2+
Oxidation state of I is (-1) and for CO it is zero. Let's assume that the oxidation state of Fe in Fe(CO)₄I₂<span> (s) is x. For whole compound, the charge is zero.
Sum of oxidation numbers in all elements = Charge of the compound.
Here we have 1Fe , 4CO and 2I
hence we can find the oxidation state as;
x + 4*0 + 2*(-1) = 0
x + 0 - 2 = 0
x = +2
Hence the oxidation state of Fe in product </span>Fe(CO)₄I₂ (s) is +2.
Same as we can find the oxidation state (y) of Fe in Fe(CO)₅(s).
y + 5*0 = 0
y = 0
Since oxidation state of Fe increased from 0 to +2, the oxidized element is Fe in the given reaction.
Answer:
pH = 1.32
Explanation:
H₂M + KOH ------------------------ HM⁻ + H₂O + K⁺
This problem involves a weak diprotic acid which we can solve by realizing they amount to buffer solutions. In the first deprotonation if all the acid is not consumed we will have an equilibrium of a wak acid and its weak conjugate base. Lets see:
So first calculate the moles reacted and produced:
n H₂M = 0.864 g/mol x 1 mol/ 116.072 g = 0.074 mol H₂M
54 mL x 1L / 1000 mL x 0. 0.276 moles/L = 0.015 mol KOH
it is clear that the maleic acid will not be completely consumed, hence treat it as an equilibrium problem of a buffer solution.
moles H₂M left = 0.074 - 0.015 = 0.059
moles HM⁻ produced = 0.015
Using the Henderson - Hasselbach equation to solve for pH:
ph = pKₐ + log ( HM⁻/ HA) = 1.92 + log ( 0.015 / 0.059) = 1.325
Notes: In the HH equation we used the moles of the species since the volume is the same and they will cancel out in the quotient.
For polyprotic acids the second or third deprotonation contribution to the pH when there is still unreacted acid ( Maleic in this case) unreacted.
