EBK GET READY FOR ORGANIC CHEMISTRY
EBK GET READY FOR ORGANIC CHEMISTRY
2nd Edition
ISBN: 9780321830555
Author: KARTY
Publisher: VST
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Chapter 13, Problem 13.23P
Interpretation Introduction

(a)

Interpretation:

Consider the given synthetic schemes I and II, both of which produce the same eight-carbon target. For each synthesis scheme, it is to be determined whether it is linear or convergent.

Concept introduction:

A linear synthesis is a synthesis composed of sequential steps. In a convergent synthesis, portions of a target molecule are synthesized separately and are assembled together at a later stage.

Interpretation Introduction

(b)

Interpretation:

Consider the given synthetic schemes I and II, both of which produce the same eight-carbon target. For each synthesis scheme, assuming that each synthetic step proceeds with an 80 % yield, the overall percent yield is to be computed.

Concept introduction:

For a linear synthesis, the overall percent yield is equal to the product of the yields of each individual steps. For convergent synthesis, the overall percent yield is equal to the product of the yields of the steps of the longest branch of the synthesis.

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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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