I recently took part in the nsw titration competition and in the first part, we put unknown concentration of NaOH in burette, and 25mL of 0.1292mol/L of HCL in the conical flask. Then we put 3 drops of phenolphthalein indicator into the conical flask, and let the NaOH run into the conical flask until the solution in the flask turned a light pink colour. From this we recorded the volume and found out the concentration of the NaOH solution.
But my question is how come we can you can still use PHENOLPHTHALEIN (meant to be used when equivalence point is between 8.3 - 10 pH), when we are using a STRONG ACID and a STRONG BASE, which means it will have an equivalence point of 7.
But my question is how come we can you can still use PHENOLPHTHALEIN (meant to be used when equivalence point is between 8.3 - 10 pH), when we are using a STRONG ACID and a STRONG BASE, which means it will have an equivalence point of 7.