(a)
Interpretation:
The pI value for the given set of amino acids needs to be calculated.
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.
To find : To find the pI value of L-alanine
(b)
Interpretation:
The pI value for the given set of amino acids needs to be calculated.
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.
To find : To find the pI value of L-asparagine
(c)
Interpretation:
The pI value for the given set of amino acids needs to be calculated.
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.
To find : To find the pI value of L-histidine
(d)
Interpretation:
The pI value for the given set of amino acids needs to be calculated.
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.
To find : To find the pI value of L-glutamic acid
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Chapter 25 Solutions
ORGANIC CHEMISTRY (LL) >CUSTOM PACKAGE<
- Diels Alder Cycloaddition: Focus on regiochemistry (problems E-F) –> match + of thedienophile and - of the diene while also considering stereochemistry (endo).arrow_forwardHELP! URGENT! PLEASE RESOND ASAP!arrow_forwardQuestion 4 Determine the rate order and rate constant for sucrose hydrolysis. Time (hours) [C6H12O6] 0 0.501 0.500 0.451 1.00 0.404 1.50 0.363 3.00 0.267 First-order, k = 0.210 hour 1 First-order, k = 0.0912 hour 1 O Second-order, k = 0.590 M1 hour 1 O Zero-order, k = 0.0770 M/hour O Zero-order, k = 0.4896 M/hour O Second-order, k = 1.93 M-1-hour 1 10 ptsarrow_forward
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- Problem 5-31 Which of the following objects are chiral? (a) A basketball (d) A golf club (b) A fork (c) A wine glass (e) A spiral staircase (f) A snowflake Problem 5-32 Which of the following compounds are chiral? Draw them, and label the chirality centers. (a) 2,4-Dimethylheptane (b) 5-Ethyl-3,3-dimethylheptane (c) cis-1,4-Dichlorocyclohexane Problem 5-33 Draw chiral molecules that meet the following descriptions: (a) A chloroalkane, C5H11Cl (c) An alkene, C6H12 (b) An alcohol, C6H140 (d) An alkane, C8H18 Problem 5-36 Erythronolide B is the biological precursor of erythromycin, a broad-spectrum antibiotic. How H3C CH3 many chirality centers does erythronolide B have? OH Identify them. H3C -CH3 OH Erythronolide B H3C. H3C. OH OH CH3arrow_forwardPLEASE HELP! URGENT! PLEASE RESPOND!arrow_forward2. Propose a mechanism for this reaction. ہلی سے ملی N H (excess)arrow_forward
- Steps and explanationn please.arrow_forwardProblem 5-48 Assign R or S configurations to the chirality centers in ascorbic acid (vitamin C). OH H OH HO CH2OH Ascorbic acid O H Problem 5-49 Assign R or S stereochemistry to the chirality centers in the following Newman projections: H Cl H CH3 H3C. OH H3C (a) H H H3C (b) CH3 H Problem 5-52 Draw the meso form of each of the following molecules, and indicate the plane of symmetry in each: OH OH (a) CH3CHCH2CH2CHCH3 CH3 H3C. -OH (c) H3C CH3 (b) Problem 5-66 Assign R or S configurations to the chiral centers in cephalexin, trade-named Keflex, the most widely prescribed antibiotic in the United States. H2N H IHH S Cephalexin N. CH3 CO₂Harrow_forwardSteps and explanationn please.arrow_forward
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