ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
10th Edition
ISBN: 9781260008562
Author: Carey
Publisher: MCG
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Chapter 24.12, Problem 14P
Interpretation Introduction

Interpretation:

The reasons for the classifications in the structural formula for N-acetylneuraminic acid described as a ketose is to be explained and carbon atoms in the nine-carbon chain are to be numbered and the configuration of the highest numbered chirality center is to be determined.

Concept introduction:

In carbohydrates, if one of hydroxyl groups is replaced by an amino group, then the sugar is called amino sugar.

The sugar is a ketose sugar in which the anomeric carbon of a pyranose ring bears both, the hydroxyl group and a carbon substituent.

In carbohydrates, there is a possibility of replacement of one or more hydroxyl substituents by some other atoms.

The carbon atom with the highest oxidation state is given number one.

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For each reaction below, decide if the first stable organic product that forms in solution will create a new CC bond, and check the appropriate box. Next, for each reaction to which you answered "Yes" to in the table, draw this product in the drawing area below. Note for advanced students: for this problem, don't worry if you think this product will continue to react under the current conditions - just focus on the first stable product you expect to form in solution. ? Will the first MgBr product that forms in this reaction create a new CC bond? olo ? OH جمله O Yes Ⓒ No MgCl ? Will the first product that forms in this reaction create a new CC bond? Click and drag to start drawing a structure. Yes No X ☐ : ☐ टे PH
Assign all the protons
PROPOSE REACTION MECHANISM FOR ACID-CATALYZED REACTION OF 3-PENTANONE WITH DIMETHYLAMINE
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