Organic Chemistry (6th Edition)
Organic Chemistry (6th Edition)
6th Edition
ISBN: 9781260119107
Author: Janice Gorzynski Smith
Publisher: McGraw Hill Education
bartleby

Concept explainers

Question
Book Icon
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.

Blurred answer
Students have asked these similar questions
What would be the product if D-talose is reacted with:1. NH2OH then (CH3CO)2O, NaOCOCH3 then NaOCH3, then HNO3, H2O [note this is a consectutive reaction] 2. oxidation using HNO3
Draw the products formed when α-D-galactose is treated with each reagent: i. CH3I (excess), Ag2O ii. CH3OH, H3O+ iii. NaOH, H2O iv. Br2, H2O
Draw the products formed when β-D-galactose is treated with each reagent. a. Ag2O + CH3I b. NaH + C6H5CH2Cl c. The product in (b), then H3O+ d. Ac2O + pyridine e. C6H5COCl + pyridine f. The product in (c), then C6H5COCl + pyridine

Chapter 26 Solutions

Organic Chemistry (6th Edition)

Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning