Organic Chemistry (8th Edition)
Organic Chemistry (8th Edition)
8th Edition
ISBN: 9780134042282
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 20, Problem 40P
Interpretation Introduction

Interpretation:

The product obtained from the reaction of D-ribose with one equivalent of methanol and HCl is to be predicted.

Concept Introduction:

The hydroxyl group of anomeric carbon is protonated by an acid.  The lone pair on the ring helps in eliminating a molecule of water which results in the formation of oxocarbenium ion.  It is planar molecule.  When the alcohol approaches from the top of the plane, the β-glycoside is formed.  When the alcohol approaches from the bottom of plane, the α-glycoside is formed.

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D-Arabinose can exist in both pyranose and furanose forms.a. Draw the a and ß anomers of D-arabinofuranose.b. Draw the a and ß anomers of D-arabinopyranose
The reaction of D-ribose with one equivalent of methanol plus HCl forms four products. Draw the products.
Part A What are glycosides, and how can they be formed? A glycoside is the acetal product that results from rerction of the hemiacetal -OH group of a carbohydrate with an aldehyd O A glycoside is the acetal product that results from reaction of the hemiacetal-OH group of a carbohydrate with an alcohol. A glycoside is the hemiacetal product that results from reaction of the acetal-OH group of a carbohydrate with an alcohol. Submit Previous Answers Request Answer

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Organic Chemistry (8th Edition)

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