Organic Chemistry
Organic Chemistry
8th Edition
ISBN: 9781337516402
Author: Brown
Publisher: Cengage
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Chapter 25, Problem 25.9P
Interpretation Introduction

Interpretation:

In aldopentose, the carbon which determines the D and L configurations has to be determined.

Concept Introduction:

The D and L configurations can be defined by the –OH group present on the penultimate carbon.  If the –OH group is present on the right side of the carbon atom, it is said to be D-form (dextrorotatory form).  If the –OH group is present on the left side of the carbon atom, it is said to be L-form (levorotatory form).

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You are asked to use curved arrows to generate the significant resonance structures for the following series of compounds and to label the most significant contributor. Identify the errors that would occur if you do not expand the Lewis structures or double-check the mechanisms. Also provide the correct answers.
how to get limiting reactant and % yield based off this data Compound Mass 6) Volume(mL Ben zaphone-5008 ne Acetic Acid 1. Sam L 2-propanot 8.00 Benzopin- a col 030445 Benzopin a Colone 0.06743 Results Compound Melting Point (°c) Benzopin acol 172°c - 175.8 °c Benzoping to lone 1797-180.9
Assign ALL signals for the proton and carbon NMR spectra on the following pages.
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