Organic Chemistry - Standalone book
Organic Chemistry - Standalone book
10th Edition
ISBN: 9780073511214
Author: Francis A Carey Dr., Robert M. Giuliano
Publisher: McGraw-Hill Education
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Chapter 24.14, Problem 17P
Interpretation Introduction

Interpretation:

The curved arrows are to be added to the given sequence to show the conversion of the conjugate acid of methyl-β-D-glucopyranoside to the corresponding α-anomer.

Concept introduction:

The flow of electrons in the mechanism is shown by curved arrows.

The compound methyl-β-D-glucofuranoside can be converted to its anomer using unshared electron pair on the oxygen attached to C-5 carbon atom.

The product of each step gives ideas about the bonds that break and new bonds that are formed.

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Identify the organic functional group and reaction type for the following reaction. The reactant is a(n) - carboxylic acid hexose - Aldohexose - aldotetrose -deoxyhexose -carboxylic acid tetrose - ketohexose The product is a(n) - carboxylic acid tetrose - aldotetrose -alcohol hexose -aldohexose -carboxylic acid hexose - alcohol tetrose The reaction type is - hemiacetal formation -hydrolysis -oxidation( Benedict’s) -acetal formation -reduction( hydrogenation) - mutarotation
OH НО HO OH НО Но OH ОН ОН OH What are the monosachharides that make up this trisaccharide? O a-D-glucopyranose, a-D-galactopyranose, a-D-fructofuranose a-D-glucopyranose, a-D-galactopyranose, B-D-fructofuranose a-D-glucopyranose, a-D-glucopyranose, B-D-fructofuranose a-D-galactopyranose, a-D-glucopyranose, a -D-fructofuranose
Draw the structure of the expected product when monosaccharide A undergomutarotation upon dissolving in water in the presence of Tollens reagent (AgNO3,NH4OH).
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