Organic Chemistry: Structure and Function
Organic Chemistry: Structure and Function
8th Edition
ISBN: 9781319079451
Author: K. Peter C. Vollhardt, Neil E. Schore
Publisher: W. H. Freeman
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Chapter 5.5, Problem 5.18E

(a)

Interpretation Introduction

Interpretation: The Fisher projection of the compounds needs to be drawn.

Concept Introduction: The Fisher projection is the two-dimensional presentation of the molecule at the stereocenter atom. It represents by the cross lines.

(b)

Interpretation Introduction

Interpretation: The enantiomers and diastereomers of the Aspartame needs to be determined.

Concept Introduction:The enantiomers are mirror image of each other. They are non-super imposable to each other. Diastereomers are super imposable to each other.

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What steps might you take to produce the following product from the given starting material? CI Br Он до NH2 NH2
1) The isoamyl acetate report requires eight paragraphs - four for comparison of isoamyl alcohol and isoamyl acetate (one paragraph each devoted to MS, HNMR, CNMR and IR) and four for comparison of acetic acid and isoamyl acetate ((one paragraph each devoted to MS, HNMR, CNMR and IR. 2) For MS, the differing masses of molecular ions are a popular starting point. Including a unique fragmentation is important, too. 3) For HNMR, CNMR and IR state the peaks that are different and what makes them different (usually the presence or absence of certain groups). See if you can find two differences (in each set of IR, HNMR and CNMR spectra) due to the presence or absence of a functional group. Include peak locations. Alternatively, you can state a shift of a peak due to a change near a given functional group. Including peak locations for shifted peaks, as well as what these peaks are due to. Ideally, your focus should be on not just identifying the differences but explaining them in terms of…
№3 Fill in the below boxes. HN 1. LAH 2. H3O+ NH2
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