Excess Ca(OH)2 is shaken with water to produce a saturated solution. The solution is filtered, and a 60.00 mL sample titrated with HCl requires 11.13 mL of 9.83×10−2 M HCl to reach the endpoint. calculate ksp for Ca(OH)2?

Answer 1

To calculate the (K_{sp}) for (Ca(OH)_2), we follow these steps:

  1. Determine the amount of (HCl) used: (11.13 , \text{mL} \times 9.83 \times 10^{-2} , \text{mol/L} = 1.094 \times 10^{-3} , \text{mol} , HCl)

  2. Write the neutralization reaction: (Ca(OH)_2 + 2HCl \rightarrow CaCl_2 + 2H_2O). This shows that 2 moles of (HCl) react with 1 mole of (Ca(OH)_2).

  3. Calculate moles of (Ca(OH)_2) in the sampled solution: Since it takes 2 moles of (HCl) to neutralize 1 mole of (Ca(OH)_2), the moles of (Ca(OH)_2) is half the moles of (HCl), which is (\frac{1.094 \times 10^{-3}}{2} = 5.47 \times 10^{-4} , \text{mol}).

  4. Calculate the concentration of (Ca(OH)_2) in the solution: The volume of the sample is 60.00 mL or 0.06000 L. So, the concentration of (Ca(OH)_2) is (\frac{5.47 \times 10^{-4} , \text{mol}}{0.06000 , \text{L}} = 9.12 \times 10^{-3} , \text{M}).

  5. Write the dissociation equation and expression for (K_{sp}): (Ca(OH)2(s) \rightleftharpoons Ca^{2+}(aq) + 2OH^{-}(aq)). The (K{sp}) expression is (K_{sp} = [Ca^{2+}][OH^-]^2).

  6. Calculate the ion concentrations in the saturated solution: Since the concentration of (Ca(OH)_2) in solution is (9.12 \times 10^{-3} , \text{M}), and each formula unit of (Ca(OH)_2) produces one (Ca^{2+}) ion and two (OH^{-}) ions, the concentrations are:

    • ([Ca^{2+}] = 9.12 \times 10^{-3} , \text{M})
    • ([OH^{-}] = 2 \times 9.12 \times 10^{-3} , \text{M} = 1.824 \times 10^{-2} , \text{M})
  7. Calculate (K_{sp}): Using the concentrations found, [ K_{sp} = (9.12 \times 10^{-3})(1.824 \times 10^{-2})^2 = 9.12 \times 10^{-3} \times 3.327 \times 10^{-4} = 3.03 \times 10^{-6} ]

Therefore, the (K_{sp}) for (Ca(OH)_2) is (3.03 \times 10^{-6}).

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Answer 2

#K_"sp"=3.03xx10^-6#

We work out the moles of hydroxide....

#Ca(OH)_2(aq) + 2HCl(aq) rarr CaCl_2(aq) + 2H_2O(l)#
#"Moles of HCl"=11.13*mLxx10^-3*L*mL^-1xx9.83xx10^-2*mol*L^-1=0.001094*mol#...and given this molar quantity there were HALF this molar quantity with respect to #Ca(OH)_2# in the starting #60.00*mL# aliquot....
And so #[Ca(OH)_2(aq)]=(1/2xx0.001094*mol)/(60.00*mLxx10^-3*L*mL^-1)# #=9.12xx10^-3*mol*L^-1#...
But this concentration derived from SOLUBLE #Ca(OH)_2#, the which had participated in the solubility equilibrium...
#Ca(OH)_2(s) rightleftharpoonsCa^(2+) + 2HO^-#...

for which we write the solubility expression....

#K_"sp"=[Ca^(2+)][HO^-]^2#..and we plug in the concentrations...
#=(9.12xx10^-3)xx(2xx9.12xx10^-3)^2#
#=4xx(9.12xx10^-3)^3=3.03xx10^-6#

Please check my arithmetic....no money-back guarantees...

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Answer from HIX Tutor

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

When evaluating a one-sided limit, you need to be careful when a quantity is approaching zero since its sign is different depending on which way it is approaching zero from. Let us look at some examples.

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