ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE
2nd Edition
ISBN: 9780393666144
Author: KARTY
Publisher: NORTON
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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:

ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE, 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:

ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE, 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.

ORG CHEM W/ EBOOK & SW5 + STUDY GUIDE, 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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2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled** Peak Chemical Shift (d) 5.7 1 Multiplicity multiplate .......... 5.04 double of doublet 2 4.98 double of doublet 3 4.05 doublet of quartet 4 5 LO 3.80 quartet 1.3 doublet 6 Peak Chemical Shift (d) Multiplicity
Interpreting NMR spectra is a skill that often requires some amount of practice, which, in turn, necessitates access to a collection of NMR spectra. Beyond Labz Organic Synthesis and Organic Qualitative Analysis have spectral libraries containing over 700 1H NMR spectra. In this assignment, you will take advantage of this by first predicting the NMR spectra for two closely related compounds and then checking your predictions by looking up the actual spectra in the spectra library. After completing this assignment, you may wish to select other compounds for additional practice. 1. Write the IUPAC names for the following two structures: Question 2 Question 3 2. Predict the NMR spectra for each of these two compounds by listing, in the NMR tables below, the chemical shift, the splitting, and the number of hydrogens associated with each predicted peak. Sort the peaks from largest chemical shift to lowest. **Not all slots must be filled**
11:14 ... worksheets.beyondlabz.com 3. To check your predictions, click this link for Interpreting NMR Spectra 1. You will see a list of all the - compounds in the spectra library in alphabetical order by IUPAC name. Hovering over a name in the list will show the structure on the chalkboard. The four buttons on the top of the Spectra tab in the tray are used to select the different spectroscopic techniques for the selected compound. Make sure the NMR button has been selected. 4. Scroll through the list of names to find the names for the two compounds you have been given and click on the name to display the NMR spectrum for each. In the NMR tables below, list the chemical shift, the splitting, and the number of hydrogens associated with each peak for each compound. Compare your answers to your predictions. **Not all slots must be filled** Peak Chemical Shift (d) Multiplicity 1 2 3 4 5

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