Percent Dissociated from Titration Curve Announcing the arrival of Valued Associate #679: Cesar Manara Planned maintenance scheduled April 23, 2019 at 00:00UTC (8:00pm US/Eastern)Volume required to dilute solution for a pH changeHow to calculate the composition of a borate buffer with a defined pH using the Henderson-Hasselbalch equation?Titration of alpha-amino acid with strong baseWhy do these two calculations give me different answers for the same acid-base titration?Titration of NaOH with acetic acidUnderstanding how to calculate the pH of a buffer with ice tablesTitration with Ca(OH)2calculating ph of a mixture of acidsFinding the concentration of hydrochloric acid by titrationWhy does pH increase as a weak acid becomes more dissociated?

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Percent Dissociated from Titration Curve



Announcing the arrival of Valued Associate #679: Cesar Manara
Planned maintenance scheduled April 23, 2019 at 00:00UTC (8:00pm US/Eastern)Volume required to dilute solution for a pH changeHow to calculate the composition of a borate buffer with a defined pH using the Henderson-Hasselbalch equation?Titration of alpha-amino acid with strong baseWhy do these two calculations give me different answers for the same acid-base titration?Titration of NaOH with acetic acidUnderstanding how to calculate the pH of a buffer with ice tablesTitration with Ca(OH)2calculating ph of a mixture of acidsFinding the concentration of hydrochloric acid by titrationWhy does pH increase as a weak acid becomes more dissociated?










2












$begingroup$


enter image description here



Question 818 references the titration curve. Answer is A because $ceH+$ conc $= 10^-4$. This is conc of dissociated acid. The conc of the undissociated acid is the original concentration minus this: $0.1 - 0.0001$, which is about $0.1$. So then its $frac0.00010.1times 100 = 0.1%$.



Where in the world are they getting the original concentration? how did they get $0.1$ as the concentration of undissociated acid?










share|improve this question











$endgroup$
















    2












    $begingroup$


    enter image description here



    Question 818 references the titration curve. Answer is A because $ceH+$ conc $= 10^-4$. This is conc of dissociated acid. The conc of the undissociated acid is the original concentration minus this: $0.1 - 0.0001$, which is about $0.1$. So then its $frac0.00010.1times 100 = 0.1%$.



    Where in the world are they getting the original concentration? how did they get $0.1$ as the concentration of undissociated acid?










    share|improve this question











    $endgroup$














      2












      2








      2





      $begingroup$


      enter image description here



      Question 818 references the titration curve. Answer is A because $ceH+$ conc $= 10^-4$. This is conc of dissociated acid. The conc of the undissociated acid is the original concentration minus this: $0.1 - 0.0001$, which is about $0.1$. So then its $frac0.00010.1times 100 = 0.1%$.



      Where in the world are they getting the original concentration? how did they get $0.1$ as the concentration of undissociated acid?










      share|improve this question











      $endgroup$




      enter image description here



      Question 818 references the titration curve. Answer is A because $ceH+$ conc $= 10^-4$. This is conc of dissociated acid. The conc of the undissociated acid is the original concentration minus this: $0.1 - 0.0001$, which is about $0.1$. So then its $frac0.00010.1times 100 = 0.1%$.



      Where in the world are they getting the original concentration? how did they get $0.1$ as the concentration of undissociated acid?







      acid-base aqueous-solution analytical-chemistry titration






      share|improve this question















      share|improve this question













      share|improve this question




      share|improve this question








      edited Apr 1 at 17:10









      Mathew Mahindaratne

      6,393725




      6,393725










      asked Apr 1 at 14:31









      JonJon

      232




      232




















          1 Answer
          1






          active

          oldest

          votes


















          6












          $begingroup$

          I'm not sure I follow your logic.
          For a monobasic acid S $(ceHA)$ dissociation degree $α$ is



          $$α = frac[ceH+]c_mathrma,$$



          where $c_mathrma$ is the initial concentration of the acid which you are determining via titration with the defined volume of a strong base $V_mathrmb$:



          $$c_mathrmaV_mathrma = c_mathrmbV_mathrmb implies c_mathrma = fracc_mathrmbV_mathrmbV_mathrma$$



          Finally, taking $V_mathrma = V_mathrmb = pu50 mL$ (from the figure's caption and equilibrium point) and, as you already assumed from pH, $[ceH+] approx pu1e-4 mol L-1$:



          $$α = frac[ceH+]V_mathrmac_mathrmbV_mathrmb = fracpu1e-4 mol L-1cdotpu50 mLpu0.1 mol L-1cdotpu50 mL = pu1e-3~textor~0.1%$$






          share|improve this answer









          $endgroup$








          • 1




            $begingroup$
            Thank you! I appreciate your help. I seem to have missed the entire purpose of the titration... so the idea is that you are setting the molar amount of base to the molar amount of acid specifically at the equivalence point, then solving for the original concentration of acid. then you divide the hydrogen ion concentration by this value
            $endgroup$
            – Jon
            Apr 1 at 15:00












          Your Answer








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          1 Answer
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          active

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          active

          oldest

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          6












          $begingroup$

          I'm not sure I follow your logic.
          For a monobasic acid S $(ceHA)$ dissociation degree $α$ is



          $$α = frac[ceH+]c_mathrma,$$



          where $c_mathrma$ is the initial concentration of the acid which you are determining via titration with the defined volume of a strong base $V_mathrmb$:



          $$c_mathrmaV_mathrma = c_mathrmbV_mathrmb implies c_mathrma = fracc_mathrmbV_mathrmbV_mathrma$$



          Finally, taking $V_mathrma = V_mathrmb = pu50 mL$ (from the figure's caption and equilibrium point) and, as you already assumed from pH, $[ceH+] approx pu1e-4 mol L-1$:



          $$α = frac[ceH+]V_mathrmac_mathrmbV_mathrmb = fracpu1e-4 mol L-1cdotpu50 mLpu0.1 mol L-1cdotpu50 mL = pu1e-3~textor~0.1%$$






          share|improve this answer









          $endgroup$








          • 1




            $begingroup$
            Thank you! I appreciate your help. I seem to have missed the entire purpose of the titration... so the idea is that you are setting the molar amount of base to the molar amount of acid specifically at the equivalence point, then solving for the original concentration of acid. then you divide the hydrogen ion concentration by this value
            $endgroup$
            – Jon
            Apr 1 at 15:00
















          6












          $begingroup$

          I'm not sure I follow your logic.
          For a monobasic acid S $(ceHA)$ dissociation degree $α$ is



          $$α = frac[ceH+]c_mathrma,$$



          where $c_mathrma$ is the initial concentration of the acid which you are determining via titration with the defined volume of a strong base $V_mathrmb$:



          $$c_mathrmaV_mathrma = c_mathrmbV_mathrmb implies c_mathrma = fracc_mathrmbV_mathrmbV_mathrma$$



          Finally, taking $V_mathrma = V_mathrmb = pu50 mL$ (from the figure's caption and equilibrium point) and, as you already assumed from pH, $[ceH+] approx pu1e-4 mol L-1$:



          $$α = frac[ceH+]V_mathrmac_mathrmbV_mathrmb = fracpu1e-4 mol L-1cdotpu50 mLpu0.1 mol L-1cdotpu50 mL = pu1e-3~textor~0.1%$$






          share|improve this answer









          $endgroup$








          • 1




            $begingroup$
            Thank you! I appreciate your help. I seem to have missed the entire purpose of the titration... so the idea is that you are setting the molar amount of base to the molar amount of acid specifically at the equivalence point, then solving for the original concentration of acid. then you divide the hydrogen ion concentration by this value
            $endgroup$
            – Jon
            Apr 1 at 15:00














          6












          6








          6





          $begingroup$

          I'm not sure I follow your logic.
          For a monobasic acid S $(ceHA)$ dissociation degree $α$ is



          $$α = frac[ceH+]c_mathrma,$$



          where $c_mathrma$ is the initial concentration of the acid which you are determining via titration with the defined volume of a strong base $V_mathrmb$:



          $$c_mathrmaV_mathrma = c_mathrmbV_mathrmb implies c_mathrma = fracc_mathrmbV_mathrmbV_mathrma$$



          Finally, taking $V_mathrma = V_mathrmb = pu50 mL$ (from the figure's caption and equilibrium point) and, as you already assumed from pH, $[ceH+] approx pu1e-4 mol L-1$:



          $$α = frac[ceH+]V_mathrmac_mathrmbV_mathrmb = fracpu1e-4 mol L-1cdotpu50 mLpu0.1 mol L-1cdotpu50 mL = pu1e-3~textor~0.1%$$






          share|improve this answer









          $endgroup$



          I'm not sure I follow your logic.
          For a monobasic acid S $(ceHA)$ dissociation degree $α$ is



          $$α = frac[ceH+]c_mathrma,$$



          where $c_mathrma$ is the initial concentration of the acid which you are determining via titration with the defined volume of a strong base $V_mathrmb$:



          $$c_mathrmaV_mathrma = c_mathrmbV_mathrmb implies c_mathrma = fracc_mathrmbV_mathrmbV_mathrma$$



          Finally, taking $V_mathrma = V_mathrmb = pu50 mL$ (from the figure's caption and equilibrium point) and, as you already assumed from pH, $[ceH+] approx pu1e-4 mol L-1$:



          $$α = frac[ceH+]V_mathrmac_mathrmbV_mathrmb = fracpu1e-4 mol L-1cdotpu50 mLpu0.1 mol L-1cdotpu50 mL = pu1e-3~textor~0.1%$$







          share|improve this answer












          share|improve this answer



          share|improve this answer










          answered Apr 1 at 14:50









          andseliskandselisk

          19.7k665128




          19.7k665128







          • 1




            $begingroup$
            Thank you! I appreciate your help. I seem to have missed the entire purpose of the titration... so the idea is that you are setting the molar amount of base to the molar amount of acid specifically at the equivalence point, then solving for the original concentration of acid. then you divide the hydrogen ion concentration by this value
            $endgroup$
            – Jon
            Apr 1 at 15:00













          • 1




            $begingroup$
            Thank you! I appreciate your help. I seem to have missed the entire purpose of the titration... so the idea is that you are setting the molar amount of base to the molar amount of acid specifically at the equivalence point, then solving for the original concentration of acid. then you divide the hydrogen ion concentration by this value
            $endgroup$
            – Jon
            Apr 1 at 15:00








          1




          1




          $begingroup$
          Thank you! I appreciate your help. I seem to have missed the entire purpose of the titration... so the idea is that you are setting the molar amount of base to the molar amount of acid specifically at the equivalence point, then solving for the original concentration of acid. then you divide the hydrogen ion concentration by this value
          $endgroup$
          – Jon
          Apr 1 at 15:00





          $begingroup$
          Thank you! I appreciate your help. I seem to have missed the entire purpose of the titration... so the idea is that you are setting the molar amount of base to the molar amount of acid specifically at the equivalence point, then solving for the original concentration of acid. then you divide the hydrogen ion concentration by this value
          $endgroup$
          – Jon
          Apr 1 at 15:00


















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