EBK GET READY FOR ORGANIC CHEMISTRY
EBK GET READY FOR ORGANIC CHEMISTRY
2nd Edition
ISBN: 8220100576379
Author: KARTY
Publisher: PEARSON
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Chapter E, Problem E.28P
Interpretation Introduction

(a)

Interpretation:

For the given molecule, the complete IUPAC name is to be written.

Concept introduction:

To write the IUPAC name, first it is important to determine the highest-priority functional group present that requires a suffix referring to Table E-1. In the molecule that contains both, an OH and a NH2 functional group, the functional group OH gets priority over NH2 functional group, and -ol is added as a suffix to the IUPAC name. Next, the main chain or ring containing the highest-priority functional group is to be determined. The next step is to number the main chain or ring such that carbon atoms involving the highest-priority functional group receive the lowest possible numbers. The locator number for the highest-priority functional group is written immediately before the suffix, unless needed. All other functional groups in the molecule are treated as substituents and appear in the name as a prefix. Prefixes such as ‘di’, ‘tri’, ‘tetra’... etc. are used to indicate the number of identical substituents attached. The substituents are written in the alphabetical order.

Interpretation Introduction

(b)

Interpretation:

For the given molecule, the complete IUPAC name is to be written.

Concept introduction:

To write the IUPAC name, first it is important to determine the highest-priority functional group present that requires a suffix referring to Table E-1. The molecule that contains both, an OH and a NH2 functional group, the functional group OH gets priority over NH2 functional group, and the -ol is added as a suffix to the IUPAC name. Next, the main chain or ring containing the highest-priority functional group is to be determined. The next step is to number the main chain or ring such that carbon atoms involving the highest-priority functional group receive the lowest possible numbers. The locator number for the highest-priority functional group is written immediately before the suffix, unless needed. All other functional groups in the molecule are treated as substituents and appear in the name as a prefix. Prefixes like ‘di’, ‘tri’, ‘tetra’… etc. are used to indicate the number of identical substituents attached. The substituents are written in the alphabetical order.

Interpretation Introduction

(c)

Interpretation:

For the given molecule, the complete IUPAC name is to be written.

Concept introduction:

To write the IUPAC name, first it is important to determine the highest-priority functional group present that requires a suffix referring to Table E-1. The molecule that contains both, an OH and a NH2 functional group, the functional group OH gets priority over NH2 functional group, and the -ol is added as a suffix to the IUPAC name. Next, the main chain or ring containing the highest-priority functional group is to be determined. The next step is to number the main chain or ring such that carbon atoms involving the highest-priority functional group receive the lowest possible numbers. The locator number for the highest-priority functional group is written immediately before the suffix, unless needed. All other functional groups in the molecule are treated as substituents and appear in the name as a prefix. Prefixes such as ‘di’, ‘tri’, ‘tetra’... etc. are used to indicate the number of identical substituents attached. The substituents are written in the alphabetical order.

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Done 11:14 ⚫ worksheets.beyondlabz.com 5 (a). Using the peak information you listed in the tables for both structures, assign each peak to that portion of the structure that produces the peak in the NMR spectrum. Draw this diagram on your own sheet of paper and attach the sketch of your drawing to this question. Question 6 5 (b). Using the peak information you listed in the tables for both structures, assign each peak to that portion of the structure that produces the peak in the NMR spectrum. Draw this diagram on your own sheet of paper and attach the sketch of your drawing to this question. Question 7 6. Are there any differences between the spectra you obtained in Beyond Labz and the predicted spectra? If so, what were the differences? <
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
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