EBK ORGANIC CHEMISTRY
EBK ORGANIC CHEMISTRY
8th Edition
ISBN: 8220102744127
Author: Bruice
Publisher: PEARSON
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Chapter 21.5, Problem 18P

(a)

Interpretation Introduction

Interpretation:

The order of elution of aspartate before serine by pH-4 buffer through a column packed Dowex-50 should be explained.

Concept introduction:

Ion-exchange chromatography is used to separate mixture of amino acids on the basis of their overall charge by using cation or anion-exchange resins.

Dowex-50 is a cation-exchange resins with less polar used for Cation-exchange chromatography.

Cation-exchange chromatography separate amino acids according to their pI values, the lesser the pI-value of an amino acid as compared to given pH have the high concentration of negative charged ions. The negative charged ions elute (release from chromatogram) easily from the Cation-exchange chromatogram. And if the amino acids are more polar, then it will also elute (release from chromatogram) easily by the non-polar resins (Dowex-50).

(b)

Interpretation Introduction

Interpretation:

The order of elution of serine before alanine by pH-4 buffer through a column packed Dowex-50 should be explained.

Concept introduction:

Ion-exchange chromatography is used to separate mixture of amino acids on the basis of their overall charge by using cation or anion-exchange resins.

Dowex-50 is a cation-exchange resins with less polar used for Cation-exchange chromatography.

Cation-exchange chromatography separate amino acids according to their pI values and polarities, the lesser the pI-value of an amino acid as compared to given pH have the high concentration of negative charged ions. The negative charged ions elute (release from chromatogram) easily from the Cation-exchange chromatogram. And if an amino acid is more polar, then it will also elute (release from chromatogram) easily by the non-polar resins (Dowex-50).

(c)

Interpretation Introduction

Interpretation:

The order of elution of valine before leucine by pH-4 buffer through a column packed Dowex-50 should be explained.

Concept introduction:

Ion-exchange chromatography is used to separate mixture of amino acids on the basis of their overall charge by using cation or anion-exchange resins.

Dowex-50 is a cation-exchange resins with less polar used for Cation-exchange chromatography.

Cation-exchange chromatography separate amino acids according to their pI values and polarities, the lesser the pI-value of an amino acid as compared to given pH have the high concentration of negative charged ions. The negative charged ions elute (release from chromatogram) easily from the Cation-exchange chromatogram. And if an amino acid is more polar, then it will also elute (release from chromatogram) easily by the non-polar resins (Dowex-50).

(d)

Interpretation Introduction

Interpretation:

The order of elution of tyrosine before phenylalanine by pH-4 buffer through a column packed Dowex-50 should be explained.

Concept introduction:

Ion-exchange chromatography is used to separate mixture of amino acids on the basis of their overall charge by using cation or anion-exchange resins.

Dowex-50 is a cation-exchange resins with less polar used for Cation-exchange chromatography.

Cation-exchange chromatography separate amino acids according to their pI values and polarities, the lesser the pI-value of an amino acid as compared to given pH have the high concentration of negative charged ions. The negative charged ions elute (release from chromatogram) easily from the Cation-exchange chromatogram. And if an amino acid is more polar, then it will also elute (release from chromatogram) easily by the non-polar resins (Dowex-50).

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Metalloprotein linkages are most likely to be formed between: Select one: O a. Two cysteines O b. An arginine and a glutamic acid O c. Aleucine and a phenylalanine O d. Two aspartate residues O e, A tyrosine and a serine Previous page Time left 1:29:48 OL DCE DELL
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Explain the order of elution (with a buffer of pH 4) of the following pairs of amino acids through a column packed with Dowex 50 a. aspartate before serine           c. valine before leucine b. serine before alanine              d. tyrosine before phenylalanine

Chapter 21 Solutions

EBK ORGANIC CHEMISTRY

Ch. 21.4 - Prob. 13PCh. 21.4 - Explain why the pI of lysine is the average of the...Ch. 21.5 - What aldehyde is formed when valine is treated...Ch. 21.5 - Prob. 16PCh. 21.5 - Prob. 17PCh. 21.5 - Prob. 18PCh. 21.5 - Prob. 19PCh. 21.6 - Why is excess ammonia used in the preceding...Ch. 21.6 - Prob. 21PCh. 21.6 - What amino acid is formed using the...Ch. 21.6 - Prob. 23PCh. 21.6 - What amino acid is formed when the aldehyde used...Ch. 21.7 - Esterase is an enzyme that catalyzes the...Ch. 21.8 - Draw the tetrapeptide Ala-Thr-Asp-Asn and indicate...Ch. 21.8 - Draw the resonance contributors of the peptide...Ch. 21.8 - Which bonds in the backbone of a peptide can...Ch. 21.9 - An opioid pentapeptide has the following...Ch. 21.9 - What is the configuration about each of the...Ch. 21.9 - Glutathione is a tripeptide whose function is to...Ch. 21.10 - What dipeptides would be formed by heating a...Ch. 21.10 - Suppose you are trying to synthesize the dipeptide...Ch. 21.10 - Show the steps in the synthesis of the...Ch. 21.10 - a. Calculate the overall yield of bradykinin when...Ch. 21.11 - Show the steps in the synthesis of the...Ch. 21.13 - Prob. 37PCh. 21.13 - In determining the primary structure of insulin,...Ch. 21.13 - A decapeptide undergoes partial hydrolysis to give...Ch. 21.13 - Explain why cyanogen bromide does not cleave on...Ch. 21.13 - Indicate the peptides produced from cleavage by...Ch. 21.14 - Prob. 43PCh. 21.14 - Three peptides were obtained from a trypsin...Ch. 21.14 - Prob. 45PCh. 21.15 - How would a protein that resides in the nonpolar...Ch. 21.16 - a. Which would have the greatest percentage of...Ch. 21.17 - When apples that have been cut are exposed to...Ch. 21 - Glycine has pK2 values of 2.34 and 9.60. At what...Ch. 21 - Prob. 50PCh. 21 - A titration curve is a plot of the pH of a...Ch. 21 - Prob. 52PCh. 21 - Aspartame (its structure is on page 1007) has a pl...Ch. 21 - Draw the form of aspartate that predominates at...Ch. 21 - Show how phenylalanine can be prepared by...Ch. 21 - A professor was preparing a manuscript for...Ch. 21 - What aldehydes are formed when the following amino...Ch. 21 - Prob. 58PCh. 21 - Determine the amino acid sequence of a polypeptide...Ch. 21 - Prob. 60PCh. 21 - Prob. 61PCh. 21 - Which is the more effective buffer at...Ch. 21 - Identify the location and type of charge on the...Ch. 21 - Draw the product obtained when a lysine side chain...Ch. 21 - After the polypeptide shown below was treated with...Ch. 21 - Treatment of a polypeptide with 2-mercaptoethanol...Ch. 21 - Show how aspartame can be synthesized using DCCD.Ch. 21 - -Amino acids can be prepared by treating an...Ch. 21 - Reaction of a polypeptide with carboxypeptidase A...Ch. 21 - a. How many different octapeptides can be made...Ch. 21 - Glycine has pKa values of 2.3 and 9.6. Do you...Ch. 21 - A mixture of 15 amino acids gave the fingerprint...Ch. 21 - Write the mechanism for the reaction of an amino...Ch. 21 - Prob. 74PCh. 21 - Show how valine can be prepared by a. a...Ch. 21 - The primary structure of -endorphin, a peptide...Ch. 21 - A chemist wanted to test his hypothesis that the...Ch. 21 - Propose a mechanism for the rearrangement of the...Ch. 21 - A normal polypeptide and a mutant of the...Ch. 21 - Determine the amino acid sequence of a polypeptide...
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