
Interpretation:
The graph for the titration of tetrabasic base with strong acid,
Concept Introduction:-
Titration of tetrabasic base with strong acid:
When a strong acid is titrated against tetrabasic base, there is an equivalence or stoichiometric point, when an H+ is dissociated then there are multiple equivalence points. The equivalence point will occur when the moles of the strong acid added to same amount of the moles of weak base present. However, when a weak polyprotic acid is titrated. Therefore, the number of equivalence points depends on the number of H+ atoms that can be removed from the molecule.
Spreadsheet Equation for titration of titration of tetrabasic base with strong acid:
Where,

Want to see the full answer?
Check out a sample textbook solution
Chapter 11 Solutions
Quantitative Chemical Analysis
- Nucleophilic Aromatic Substitution: What is the product of the reaction? What is the name of the intermediate complex? *See imagearrow_forwardPredict the final product. If 2 products are made, list which should be “major” and “minor” *see attachedarrow_forwardNucleophilic Aromatic Substitution: What is the product of the reaction? *see imagearrow_forward
- Show the correct sequence to connect the reagent to product. * see imagearrow_forwardThe answer here says that F and K have a singlet and a doublet. The singlet and doublet are referring to the H's 1 carbon away from the carbon attached to the OH. Why don't the H's two carbons away, the ones on the cyclohexane ring, cause more peaks on the signal?arrow_forwardDraw the Birch Reduction for this aromatic compound and include electron withdrawing groups and electron donating groups. *See attachedarrow_forward
- Show the correct sequence to connect the reagent to product. * see imagearrow_forwardBlocking Group are use to put 2 large sterically repulsive group ortho. Show the correct sequence toconnect the reagent to product with the highest yield possible. * see imagearrow_forwardElimination-Addition: What molecule was determined to be an intermediate based on a “trapping experiment”? *please solve and see imagearrow_forward
- ChemistryChemistryISBN:9781305957404Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCostePublisher:Cengage LearningChemistryChemistryISBN:9781259911156Author:Raymond Chang Dr., Jason Overby ProfessorPublisher:McGraw-Hill EducationPrinciples of Instrumental AnalysisChemistryISBN:9781305577213Author:Douglas A. Skoog, F. James Holler, Stanley R. CrouchPublisher:Cengage Learning
- Organic ChemistryChemistryISBN:9780078021558Author:Janice Gorzynski Smith Dr.Publisher:McGraw-Hill EducationChemistry: Principles and ReactionsChemistryISBN:9781305079373Author:William L. Masterton, Cecile N. HurleyPublisher:Cengage LearningElementary Principles of Chemical Processes, Bind...ChemistryISBN:9781118431221Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. BullardPublisher:WILEY





