Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter 22, Problem 28P
Interpretation Introduction
Interpretation:
A possible synthesis of xylitol starting with appropriate monosaccharide is to be outlined.
Concept introduction:
Monosaccharides containing five carbon atoms and an
Alditols are the compounds produced from aldoses or ketoses on reduction with certain reducing agents, such as sodium borohydride (
Xylitol is an alditol and is used as a sweetener in chewing gums.
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(d) Draw the structure of the expected product when monosaccharide B undergo
mutarotation upon dissolving in water in the presence of Tollens reagent (AGNO3,
NHẠOH).
он
OH
O.
OH
OH
OH
monosaccharide B
Propose structural formulas for the following polysaccharides.
Q.) Pectic acid is the main component of pectin, which is responsible for the formation of jellies from fruits and berries. Pectic acid is a polymer of d-galacturonic acid in the pyranose form joined by a-1,4-glycosidic bonds.
Name each monosaccharide unit in stachyose and specify whether it is a d-monosaccharide or an l-monosaccharide.
Chapter 22 Solutions
Organic Chemistry
Ch. 22 - Prob. 1PPCh. 22 - Prob. 2PPCh. 22 - Prob. 3PPCh. 22 - Prob. 4PPCh. 22 - Prob. 5PPCh. 22 - Prob. 6PPCh. 22 - Prob. 7PPCh. 22 - Prob. 8PPCh. 22 - Practice Problem 22.9 What products would you...Ch. 22 - Prob. 10PP
Ch. 22 - Prob. 11PPCh. 22 - Prob. 12PPCh. 22 - Prob. 13PPCh. 22 - Prob. 14PPCh. 22 - Prob. 15PPCh. 22 - Prob. 16PPCh. 22 - Prob. 17PPCh. 22 - Prob. 18PPCh. 22 - Prob. 19PPCh. 22 - Prob. 20PCh. 22 - Prob. 21PCh. 22 - Prob. 22PCh. 22 - Prob. 23PCh. 22 - Prob. 24PCh. 22 - Prob. 25PCh. 22 - Prob. 26PCh. 22 - Prob. 27PCh. 22 - Prob. 28PCh. 22 - Prob. 29PCh. 22 - Prob. 30PCh. 22 - Prob. 31PCh. 22 - Prob. 32PCh. 22 - Prob. 33PCh. 22 - Prob. 34PCh. 22 - Prob. 35PCh. 22 - Prob. 36PCh. 22 - Prob. 37PCh. 22 - Prob. 38PCh. 22 - Arbutin, a compound that can be isolated from the...Ch. 22 - Prob. 40PCh. 22 - Prob. 41PCh. 22 - Prob. 42PCh. 22 - Prob. 43PCh. 22 - 22.44 The following reaction sequence represents...Ch. 22 - 22.45
The NMR data for the two anomers...Ch. 22 - Shikimic acid is a key biosynthetic intermediate...
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- Monosaccharides can be drawn in a variety of ways, and in truth, often a mixture of cyclic compounds is present in a solution. Identify each monosaccharide, including its proper D,L designation, drawn in a less-than-typical fashion.arrow_forwardDraw the structure of the expected product when monosaccharide A undergomutarotation upon dissolving in water in the presence of Tollens reagent (AgNO3,NH4OH).arrow_forward1arrow_forward
- Propose structural formulas for the following polysaccharides. Q.) Alginic acid, isolated from seaweed, is used as a thickening agent in ice cream and other foods. Alginic acid is a polymer of d-mannuronic acid in the pyranose form joined by b-1,4-glycosidic bonds.arrow_forward1) Phenyl propyl ether can be obtained by reacting? 2) Raffinose is A trisaccharide which is made up of two sugar molecules of aldoses and one sugar molecule of ketoses? True or false!arrow_forward(a) Convert each cyclic monosaccharide into a Fischer projection of its acyclic form. (b) Name each monosaccharide. (c) Label the anomer as a or ß.arrow_forward
- Draw a Haworth project of a common cyclic form of this monosaccharide:arrow_forwardDigitalis is a preparation made from the dried seeds and leaves of the purple foxglove, Digitalis purpurea, a plant native to southern and central Europe and cultivated in the United States. The preparation is a mixture of several active components, including digitalin. Digitalis is used in medicine to increase the force of myocardial contraction and as a conduction depressant to decrease heart rate (the heart pumps more forcefully but less often).arrow_forwardDraw the structure of: (a) a polysaccharide formed by joining D-mannose units in 1->4-ß-glycosidic linkages; (b) a polysaccharide formed by joining D-glucose units in 1->6-a-glycosidic linkages. The polysaccharide in (b) is dextran, a component of dental plaque.arrow_forward
- Give the common name of each disaccharide. a-D-glucopyranosyl – (1 à 4) -b-D-glucopyranose b-D-galactopyranosyl – (1 à 4) - a-D-glucopyranoside a-D-glucopyranosyl – (1 à 2) - b-D-fructofuranoside b-D-glucopyranosyl – (1 à 4) - b-D-glucopyranosearrow_forwardGive proper explanation and if possible don't upload any image. Hand written solutions are strictly prohibited.arrow_forwardDraw the structure of the expected product when monosaccharide A undergo mutarotation upon dissolving in water in the presence of Tollens reagent (AgNO3, NH4OH).arrow_forward
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