Organic Chemistry (6th Edition)
Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
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Chapter 26.8, Problem 19P
Interpretation Introduction

(a)

Interpretation: The products formed by the treatment of β-D-galactose with Ag2O, CH3I are to be drawn.

Concept introduction: The OH groups of monosaccharides on reaction with base and an alkyl halide convert into ether. A single product is formed during this reaction because the configuration of all substituents in the starting material is retained.

Interpretation Introduction

(b)

Interpretation: The products formed by the treatment of β-D-galactose with NaH+C6H5CH2Cl are to be drawn.

Concept introduction: The OH groups of monosaccharides on reaction with base and an alkyl halide convert into ether. A single product is formed during this reaction because the configuration of all substituents in the starting material is retained.

Interpretation Introduction

(c)

Interpretation: The products formed by the treatment of β-D-galactose with NaH+C6H5CH2Cl and then H3O+ are to be drawn.

Concept introduction: The characteristic bond of glycoside is O. A hemiacetal converts into acetal when a monosaccharide is treated with alcohol and HCl. The acetal formed is known as glycoside. The hydrolysis of glycoside generates two compounds that have OH group.

Interpretation Introduction

(d)

Interpretation: The products formed by the treatment of β-D-galactose with Ac2O+pyridine are to be drawn.

Concept introduction: The OH groups of monosaccharides on reaction with anhydride and acetyl chloride convert into ether in the presence of base. A single product is formed during this reaction because the configuration of all substituents in the starting material is retained.

Interpretation Introduction

(e)

Interpretation: The products formed by the treatment of D- galactose with C6H5COCl+pyridine are to be drawn.

Concept introduction: The OH groups of monosaccharides on reaction with anhydride and acetyl chloride convert into ether in the presence of base. A single product is formed during this reaction because the configuration of all substituents in the starting material is retained.

Interpretation Introduction

(f)

Interpretation: The products formed by the treatment of β-D-galactose with NaH+C6H5CH2Cl+H3O+ and then C6H5COCl+pyridine are to be drawn.

Concept introduction: The OH groups of monosaccharides on reaction with anhydride and acetyl chloride convert into ether in the presence of base. A single product is formed during this reaction because the configuration of all substituents in the starting material is retained.

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Draw the products formed when ß-D-galactose is treated with each reagent.a. Ag2O + CH3Ib. NaH + C6H5CH2Clc. The product in (b), then H3O+d. Ac2O + pyridinee. C6H5COCl + pyridinef. The product in (c), then C6H5COCl + pyridine
Draw the products formed when CH3CH2CH2CH2OTs is treated with each reagent.a. CH3SHb. NaOCH2CH3c. NaOHd. KOC(CH3)3
1. Classify the molecule shown according to the location of its carbonyl group and the number of carbon atoms. CH₂OH C=O PIL a. Aldotriose b. Aldotetrose Aldopentose d., Ketotriose Ketotetrose HO-C-H L CH₂OH

Chapter 26 Solutions

Organic Chemistry (6th Edition)

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