![ORGANIC CHEMISTRY, WITH SOL. MAN/ STUDY](https://compass-isbn-assets.s3.amazonaws.com/isbn_cover_images/9781119477617/9781119477617_smallCoverImage.gif)
(a)
Interpretation:
The form of amino acid that predominates are the isoelectric point need to be identified.
Concept introduction:
Amino acids at a particular pH do not migrate in an electric field. This pH is known as the isoelectric point. The isoelectric point is also known as isoionic point. At this isoelectric point the amino acid is neutral. This means that the zwitterion form predominates more over the other forms. pI is the isoelectric point and this can be given by average of the pKa.
The
The uncharged amino form will predominate if,
For the side chain the same rule applies as of for carboxylic acid and amino group.
(b)
Interpretation:
The form of amino acid that predominates are the isoelectric point need to be identified.
Concept introduction:
Amino acids at a particular pH do not migrate in an electric field. This pH is known as the isoelectric point. The isoelectric point is also known as isoionic point. At this isoelectric point the amino acid is neutral. This means that the zwitterion form predominates more over the other forms. pI is the isoelectric point and this can be given by average of the pKa.
The carboxylic acid form will predominate if,
The uncharged amino form will predominate if,
For the side chain the same rule applies as of for carboxylic acid and amino group.
(c)
Interpretation:
The form of amino acid that predominates are the isoelectric point need to be identified.
Concept introduction:
Amino acids at a particular pH do not migrate in an electric field. This pH is known as the isoelectric point. The isoelectric point is also known as isoionic point. At this isoelectric point the amino acid is neutral. This means that the zwitterion form predominates more over the other forms. pI is the isoelectric point and this can be given by average of the pKa.
The carboxylic acid form will predominate if,
The uncharged amino form will predominate if,
For the side chain the same rule applies as of for carboxylic acid and amino group.
(d)
Interpretation:
The form of amino acid that predominates are the isoelectric point need to be identified.
Concept introduction:
Amino acids at a particular pH do not migrate in an electric field. This pH is known as the isoelectric point. The isoelectric point is also known as isoionic point. At this isoelectric point the amino acid is neutral. This means that the zwitterion form predominates more over the other forms. pI is the isoelectric point and this can be given by average of the pKa.
The carboxylic acid form will predominate if,
The uncharged amino form will predominate if,
For the side chain the same rule applies as of for carboxylic acid and amino group.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 25 Solutions
ORGANIC CHEMISTRY, WITH SOL. MAN/ STUDY
- 2. 200 LOD For an unknown compound with a molecular ion of 101 m/z: a. Use the molecular ion to propose at least two molecular formulas. (show your work) b. What is the DU for each of your possible formulas? (show your work) C. Solve the structure and assign each of the following spectra. 8 6 4 2 (ppm) 150 100 50 ō (ppm) 4000 3000 2000 1500 1000 500 HAVENUMBERI-11arrow_forwardComplete the spectroscopy with structurearrow_forwardComplete the spectroscopy with structurearrow_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
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305957404/9781305957404_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781259911156/9781259911156_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305577213/9781305577213_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9780078021558/9780078021558_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781305079373/9781305079373_smallCoverImage.gif)
![Text book image](https://www.bartleby.com/isbn_cover_images/9781118431221/9781118431221_smallCoverImage.gif)