EBK EXPLORING CHEMICAL ANALYSIS
EBK EXPLORING CHEMICAL ANALYSIS
5th Edition
ISBN: 9781319416942
Author: Harris
Publisher: VST
Question
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Chapter 23, Problem 23.1P

(a)

Interpretation Introduction

Interpretation:

Principal species that will be eluted and order of elution at pH12 has to be explained.

Concept Introduction:

If pH is greater than pKa then deprotonation occurs and if pH is less than pKb then protonation occurs.

Cation exchangers contain negative bound groups that attract solute cation. And anion exchangers contain positive bound groups that attract solute anion.

(a)

Expert Solution
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Explanation of Solution

pKa of hexanoic acid is 5.09 and pKa of 1-aminohexane is 10.21, hence at pH 12.0, the reaction occurs as follows:

EBK EXPLORING CHEMICAL ANALYSIS, Chapter 23, Problem 23.1P , additional homework tip  1

At this pH, 1-aminohexane remains as it is. Therefore at pH 12, the mobile phase contains C6H11O2, Na+, OH, and C6H15N as principal species.

As cation exchanger attracts the solute cation, thus all directly passes through the cation exchange column.

(b)

Interpretation Introduction

Interpretation:

Principal species that will be eluted and order of elution at pH3 has to be explained.

Concept Introduction:

Refer to part (a).

(b)

Expert Solution
Check Mark

Explanation of Solution

At pH 3.0, reaction occurs as follows:

EBK EXPLORING CHEMICAL ANALYSIS, Chapter 23, Problem 23.1P , additional homework tip  2

At this pH, hexanoic acid remains as it is.

Therefore at pH 3.0, the mobile phase contains C6H12O2, H+, Cl, and C6H16N+ as principal species. As cation exchanger attracts the solute cation, thus all directly passes through the cation exchange column except that of C6H16N+.

So, the elute mixture contains C6H12O2, H+, and Cl.

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Please answer the question and provide a detailed drawing of the structure. If there will not be a new C – C bond, then the box under the drawing area will be checked.  Will the following reaction make a molecule with a new C – C bond as its major product:  Draw the major organic product or products, if the reaction will work. Be sure you use wedge and dash bonds if necessary, for example to distinguish between major products with different stereochemistry.
Please do not use AI.  AI cannot "see" the molecules properly, and it therefore gives the wrong answer while giving incorrect descriptions of the visual images we're looking at.  All of these compounds would be produced (I think).  In my book, I don't see any rules about yield in this case, like explaining that one product would be present in less yield for this reason or that reason.  Please explain why some of these produce less yield than others.
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