Organic Chemistry (9th Edition)
Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
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Chapter 23, Problem 23.52SP

(a)

Interpretation Introduction

To determine: The product when D-galactose reacts with Br2 and H2O.

Interpretation: The product when D-galactose reacts with Br2 and H2O is to be predicted.

Concept introduction: The reaction of aldose with bromine water gives aldonic acid. It is an oxidation reaction. Bromine water is used for this oxidation because it does not oxidize the alcohols group.

Galactose is a monosaccharide which contains six carbons and aldehyde group. It exists in D and L forms. It is formed from dietary lactose.

D-galactose is a sugar which is found in milk products.

(b)

Interpretation Introduction

To determine: The product when D-galactose reacts with NaOH,H2O.

Interpretation: The product when D-galactose reacts with NaOH,H2O is to be predicted.

Concept introduction: Galactose is a monosaccharide which contains six carbons and aldehyde group. It exists in D and L forms. It is formed from dietary lactose.

D-galactose is a sugar which is found in milk products.

(c)

Interpretation Introduction

To determine: The products when D-galactose reacts with CH3OH,H+.

Interpretation: The products when D-galactose reacts with CH3OH,H+ are to be predicted.

Concept introduction: The reaction of aldose with CH3OH,H+ gives the methyl glycosides that are more stable.

Galactose is a monosaccharide which contains six carbons and aldehyde group. It exists in D and L forms. It is formed from dietary lactose.

D-galactose is a sugar which is found in milk products.

(d)

Interpretation Introduction

To determine: The product when D-galactose reacts with Ag(NH3)2+OH.

Interpretation: The product when D-galactose reacts with Ag(NH3)2+OH is to be predicted.

Concept introduction: Galactose is a monosaccharide which contains six carbons and aldehyde group. It exists in D and L forms. It is formed from dietary lactose.

D-galactose is a sugar which is found in milk products.

The reaction of Tollens reagent Ag(NH3)2+OH with aldose gives aldonic acid and silver. Tollens test is a test for reducing sugar.

(e)

Interpretation Introduction

To determine: The product when D-galactose reacts with H2,Ni.

Interpretation: The product when D-galactose reacts with H2,Ni is to be predicted.

Concept introduction: The reaction of aldose with reducing agents H2,Ni gives alditol.

Reductions of aldose give a new asymmetric carbon atom formed in either two configurations, resulting in two epimers.

(f)

Interpretation Introduction

To determine: The product when D-galactose reacts with excess Ac2O and pyridine.

Interpretation: The product when D-galactose reacts with excess Ac2O and pyridine is to be predicted.

Concept introduction: Galactose is a monosaccharide which contains six carbons and aldehyde group. It exists in D and L forms. It is formed from dietary lactose.

D-galactose is a sugar which is found in milk products.

The reaction of aldose with excess Ac2O and pyridine to give esters is known as acylation.

(g)

Interpretation Introduction

To determine: The product when D-galactose reacts with excess CH3I,Ag2O.

Interpretation: The product when D-galactose reacts with excess CH3I,Ag2O is to be predicted.

Concept introduction: Galactose is a monosaccharide which contains six carbons and aldehyde group. It exists in D and L forms. It is formed from dietary lactose.

D-galactose is a sugar which is found in milk products.

The reaction of aldose with excess CH3I,Ag2O to give ether is known as alkylation.

(h)

Interpretation Introduction

To determine: The product when D-galactose reacts with NaBH4.

Interpretation: The product when D-galactose reacts with NaBH4 is to be predicted.

Concept introduction: The reaction of aldose with reducing agents H2,Ni and NaBH4 gives alditol. Reductions of aldose give a new asymmetric carbon atom formed in either two configurations, resulting in two epimers.

Galactose is a monosaccharide which contains six carbons and aldehyde group. It exists in D and L forms. It is formed from dietary lactose.

D-galactose is a sugar which is found in milk products.

(i)

Interpretation Introduction

To determine: The product when D-galactose reacts with given reagents.

Interpretation: The product when D-galactose reacts with given reagents is to be predicted.

Concept introduction: Ruff degradation is a method which is used to shorten sugar chain. It is a two step process which starts with a bromine-water oxidation of the aldose to its aldonic acid. Then in the second step treatment of aldonic acid with hydrogen peroxide and ferric sulfate oxidizes the carbonyl group to CO2 and give aldose with one fewer carbon atom. It is used primarily for the determination of structure and synthesis of new sugar.

(j)

Interpretation Introduction

To determine: The products when D-galactose reacts with given reagents.

Interpretation: The products when D-galactose reacts given reagents are to be predicted.

Concept introduction: The Kiliani Fischer synthesis is a method of lengthening an aldose carbon chain buy adding one carbon atom to the aldehyde end of the aldose.

In Kiliani Fischer synthesis, the first step involves the aldehyde carbon atom is made asymmetric with the formation of cyanohydrin. Then in the second step the hydrogenation of the following cyanohydrin gives two imines, which hydrolyzes to give aldehyde.

(k)

Interpretation Introduction

To determine: The products when D-galactose reacts with excess HIO4.

Interpretation: The products when D-galactose reacts with excess HIO4 are to be predicted.

Concept introduction: Galactose is a monosaccharide which contains six carbons and aldehyde group. It exists in D and L forms. It is formed from dietary lactose.

D-galactose is a sugar which is found in milk products.

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Chapter 23 Solutions

Organic Chemistry (9th Edition)

Ch. 23.4 - Prob. 23.11PCh. 23.5 - Prob. 23.12PCh. 23.5 - Prob. 23.13PCh. 23.6 - Prob. 23.14PCh. 23.6 - Prob. 23.15PCh. 23.7 - Prob. 23.16PCh. 23.7 - Prob. 23.17PCh. 23.7 - Two sugars, A and B, are known to be glucose and...Ch. 23.7 - Prob. 23.19PCh. 23.8 - Prob. 23.20PCh. 23.8 - Prob. 23.21PCh. 23.8 - Prob. 23.22PCh. 23.8 - Prob. 23.23PCh. 23.8 - Prob. 23.24PCh. 23.9 - a. Show the product that results when fructose is...Ch. 23.9 - Prob. 23.26PCh. 23.9 - Prob. 23.27PCh. 23.9 - Prob. 23.28PCh. 23.10 - Prob. 23.29PCh. 23.10 - Prob. 23.30PCh. 23.10 - Prob. 23.31PCh. 23.11 - Prob. 23.32PCh. 23.11 - The Wohl degradation, an alternative to the Ruff...Ch. 23.11 - Prob. 23.34PCh. 23.11 - Prob. 23.35PCh. 23.12A - Prob. 23.36PCh. 23.12A - Give an equation to show the reduction of Tollens...Ch. 23.12A - Prob. 23.38PCh. 23.12B - Prob. 23.39PCh. 23.12C - Prob. 23.40PCh. 23.12C - Prob. 23.41PCh. 23.13A - Prob. 23.42PCh. 23.15 - Cytosine, uracil, and guanine have tautomeric...Ch. 23.15 - a. An aliphatic aminoglycoside is relatively...Ch. 23.16C - Prob. 23.45PCh. 23 - Prob. 23.46SPCh. 23 - Prob. 23.47SPCh. 23 - Prob. 23.48SPCh. 23 - Prob. 23.49SPCh. 23 - Prob. 23.50SPCh. 23 - Prob. 23.51SPCh. 23 - Prob. 23.52SPCh. 23 - Prob. 23.53SPCh. 23 - Prob. 23.54SPCh. 23 - Prob. 23.55SPCh. 23 - Prob. 23.56SPCh. 23 - Prob. 23.57SPCh. 23 - Prob. 23.58SPCh. 23 - Prob. 23.59SPCh. 23 - Prob. 23.60SPCh. 23 - Prob. 23.61SPCh. 23 - Prob. 23.62SPCh. 23 - Prob. 23.63SPCh. 23 - Draw the structure of a four-residue segment of...Ch. 23 - Retroviruses like HIV, the pathogen responsible...Ch. 23 - Prob. 23.66SPCh. 23 - Prob. 23.67SP
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