EBK GET READY FOR ORGANIC CHEMISTRY
EBK GET READY FOR ORGANIC CHEMISTRY
2nd Edition
ISBN: 9780321787989
Author: KARTY
Publisher: PEARSON CO
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Chapter 7, Problem 7.1P
Interpretation Introduction

Interpretation:

The electron-poor H atom in methanol is to be identified, and the mechanism by which methanol acts as an acid in a proton transfer reaction with H2N is to be drawn.

Concept introduction:

An electron poor atom or a molecule is an atom or a site in a molecule that has fewer electrons than the number required for stability. In a proton transfer reaction, a proton is transferred from a Bronsted-Lowry acid (proton donor) to a Bronsted–Lowry base (proton acceptor). In an elementary step, electrons tend to flow from an electron-rich site to an electron-poor site. The curved arrow notation shows the movement of valence electrons.

Expert Solution & Answer
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Answer to Problem 7.1P

The electron-poor H atom in methanol is:

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 7, Problem 7.1P , additional homework tip  1

The mechanism by which methanol acts as an acid in a proton transfer reaction with H2N is:

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 7, Problem 7.1P , additional homework tip  2

Explanation of Solution

Atoms in CH3OH do not bear full charge. However, the high electronegativity of oxygen leads to a partial positive charge on the H to which it is bonded. Therefore, H is electron poor. H2N bears full negative charge, and therefore, it is electron rich. The curved arrow from a lone pair on N to the H atom on O represents the flow of electrons from the electron-rich site (H2N) to the electron-poor site (CH3OH). A second curved arrow is needed to make sure H has only one bond, not two.

EBK GET READY FOR ORGANIC CHEMISTRY, Chapter 7, Problem 7.1P , additional homework tip  3

Conclusion

The curved arrows are drawn from the electron-rich site (H2N) to the electron-poor site (CH3OH).

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EBK GET READY FOR ORGANIC CHEMISTRY

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