EBK ORGANIC CHEMISTRY-STUD.SOLNS.MAN+SG
EBK ORGANIC CHEMISTRY-STUD.SOLNS.MAN+SG
4th Edition
ISBN: 9781119659525
Author: Klein
Publisher: WILEY CONS
Question
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Chapter 25, Problem 51PP

(a)

Interpretation Introduction

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.

pI=pKa1+pKa22

The carboxylic acid form will predominate if, pI<pKa and carboxylate form will predominate if, pI>pKa .

The uncharged amino form will predominate if, pI>pKa and the protonated amino form will predominate if, pI<pKa .

For the side chain the same rule applies as of for carboxylic acid and amino group.

(b)

Interpretation Introduction

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.

pI=pKa1+pKa22

The carboxylic acid form will predominate if, pI<pKa and carboxylate form will predominate if, pI>pKa .

The uncharged amino form will predominate if, pI>pKa and the protonated amino form will predominate if, pI<pKa .

For the side chain the same rule applies as of for carboxylic acid and amino group.

(c)

Interpretation Introduction

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.

pI=pKa1+pKa22

The carboxylic acid form will predominate if, pI<pKa and carboxylate form will predominate if, pI>pKa .

The uncharged amino form will predominate if, pI>pKa and the protonated amino form will predominate if, pI<pKa .

For the side chain the same rule applies as of for carboxylic acid and amino group.

(d)

Interpretation Introduction

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.

pI=pKa1+pKa22

The carboxylic acid form will predominate if, pI<pKa and carboxylate form will predominate if, pI>pKa .

The uncharged amino form will predominate if, pI>pKa and the protonated amino form will predominate if, pI<pKa .

For the side chain the same rule applies as of for carboxylic acid and amino group.

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#1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hv
Don't used Ai solution
I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."

Chapter 25 Solutions

EBK ORGANIC CHEMISTRY-STUD.SOLNS.MAN+SG

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