ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<
9th Edition
ISBN: 9781337034623
Author: McMurry
Publisher: CENGAGE C
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 25.6, Problem 16P
Interpretation Introduction
Interpretation:
The products obtained either and esters.
Concept introduction:
The –OH group of the monosaccharide’s reacts to obtain the respective products.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
Predict the products formed when the following sugars react with excess acetic anhydrideand pyridine.(a) a-d-glucopyranose (b) b-d-ribofuranose
Predict the products formed when the following sugars react with excess acetic anhydrideand pyridine.(a) a-d-glucopyranose
Draw the following sugar derivatives. methyl 2,3,4,6@tetra@O@methyl@b-d-galactopyranoside2
Chapter 25 Solutions
ORGANIC CHEM.(LL)-W/OWL V2 >CUSTOM<
Ch. 25.1 - Prob. 1PCh. 25.2 - Prob. 2PCh. 25.2 - Prob. 3PCh. 25.2 - Prob. 4PCh. 25.2 - Prob. 5PCh. 25.3 - Prob. 6PCh. 25.3 - Prob. 7PCh. 25.4 - Prob. 8PCh. 25.4 - Prob. 9PCh. 25.4 - Prob. 10P
Ch. 25.5 - Prob. 11PCh. 25.5 - Prob. 12PCh. 25.5 - Prob. 13PCh. 25.5 - Prob. 14PCh. 25.5 - Prob. 15PCh. 25.6 - Prob. 16PCh. 25.6 - Prob. 17PCh. 25.6 - Prob. 18PCh. 25.6 - Prob. 19PCh. 25.6 - Prob. 20PCh. 25.6 - Prob. 21PCh. 25.6 - Prob. 22PCh. 25.6 - Prob. 23PCh. 25.7 - Prob. 24PCh. 25.8 - Show the product you would obtain from the...Ch. 25.SE - Prob. 26VCCh. 25.SE - Prob. 27VCCh. 25.SE - Prob. 28VCCh. 25.SE - Prob. 29VCCh. 25.SE - Prob. 30MPCh. 25.SE - Prob. 31MPCh. 25.SE - Glucosamine, one of the eight essential...Ch. 25.SE - D-Glicose reacts with acetone in the presence of...Ch. 25.SE - Prob. 34MPCh. 25.SE - Prob. 35MPCh. 25.SE - Prob. 36APCh. 25.SE - Prob. 37APCh. 25.SE - Prob. 38APCh. 25.SE - Prob. 39APCh. 25.SE - Prob. 40APCh. 25.SE - Assign R or S configuration to each chirality...Ch. 25.SE - Prob. 42APCh. 25.SE - Prob. 43APCh. 25.SE - Prob. 44APCh. 25.SE - Prob. 45APCh. 25.SE - Prob. 46APCh. 25.SE - Prob. 47APCh. 25.SE - Prob. 48APCh. 25.SE - Prob. 49APCh. 25.SE - Prob. 50APCh. 25.SE - Prob. 51APCh. 25.SE - Prob. 52APCh. 25.SE - Prob. 53APCh. 25.SE - Prob. 54APCh. 25.SE - Prob. 55APCh. 25.SE - Prob. 56APCh. 25.SE - Prob. 57APCh. 25.SE - Prob. 58APCh. 25.SE - Prob. 59APCh. 25.SE - Prob. 60APCh. 25.SE - Prob. 61APCh. 25.SE - Prob. 62APCh. 25.SE - Prob. 63APCh. 25.SE - D-Mannose reacts with acetone to give a...Ch. 25.SE - Prob. 65APCh. 25.SE - Prob. 66APCh. 25.SE - Prob. 67APCh. 25.SE - Prob. 68APCh. 25.SE - Prob. 69APCh. 25.SE - Prob. 70APCh. 25.SE - Prob. 71AP
Knowledge Booster
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
- product when beta-D-ribofuranose reacts with acetic anhydride in pyridienarrow_forwardProve that gentiobiose forms osazone and can undergo mutarotation can be hyrolyzed by Emulsin β-glycosidase forms these hydrolysis products following permethylation: 2,3,4,6-tetra-O-methyl-D-glucose and 2,3,4-tri-O-methyl-D-glucosearrow_forwardDraw beta-L-erythrofuranosearrow_forward
- Draw Fischer projections for the product(s) formed by reaction of d-ribose with the following. In addition, state whether each product is optically active or inactive Q. NaBH4 in H2Oarrow_forwardDraw the structure of a carbohydrate with four b-D-glucopyranosyl units connected by b(1®4) glycosidic linkages, with the second unit being connected via an a(1®6) glycosidic linkage by a side chain having two a-D-galactopyranosyl units connected by an a(1®4) glycosidic linkage.arrow_forwardDraw the following sugar derivatives. ) 2,3,4,6-tetra-O-methyl-d-mannopyranose(arrow_forward
- Give the major product that is formed when the primary hydroxyl group of the followingmonosaccharide reacts with propionic anhydride.arrow_forwardDraw the product that is obtained from the reaction of cholesterol with the following reagents a. H2, Pd/C b. acetyl chloride c. H2SO4, ∆ d. H2O, H+ e. a peroxyacidarrow_forwardAn unknown disaccharide gives a positive Tollens’ test. A glycosidase hydrolyzes it to d-galactose and d-mannose. When the disaccharide is treated with methyl iodide and Ag2O and then hydrolyzed with dilute HCl, the products are 2,3,4,6-tetra-O-methylgalactose and 2,3,4-tri-O-methylmannose. Propose a structure for the disaccharide.arrow_forward
- Write down the reactions: D-Glucopyranose + (CH3CO)2 O →arrow_forwardIndicate the product obtained by reacting alpha-D-Gulopyranose with NaBH4 in CH3OH.arrow_forwardAn unknown carbohydrate of formula C12H22O11 reacts with Tollens reagent to form asilver mirror. An a@glycosidase has no effect on the carbohydrate, but a b@galactosidasehydrolyzes it to d-galactose and d-mannose. When the carbohydrate is methylated (usingmethyl iodide and silver oxide) and then hydrolyzed with dilute HCl, the products are2,3,4,6-tetra-O-methylgalactose and 2,3,4-tri-O-methylmannose. Propose a structure forthis unknown carbohydratearrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning
Introduction to General, Organic and Biochemistry
Chemistry
ISBN:9781285869759
Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar Torres
Publisher:Cengage Learning