General, Organic, & Biological Chemistry
3rd Edition
ISBN: 9780073511245
Author: Janice Gorzynski Smith Dr.
Publisher: McGraw-Hill Education
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Question
Chapter 20.4, Problem 20.14P
Interpretation Introduction
(a)
Interpretation:
The oxidation product of the following monosaccharide needs to be drawn.
Concept Introduction:
Interpretation Introduction
(b)
Interpretation:
The oxidation product of the following monosaccharide needs to be drawn.
Concept Introduction:
Aldehyde group of the monosaccharide get oxidized in presence of the suitable oxidizing agent. Hydroxyl groups do not get affected by particular oxidizing agent.
Interpretation Introduction
(c)
Interpretation:
The oxidation product of the following monosaccharide needs to be drawn.
Concept Introduction:
Aldehyde group and
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Students have asked these similar questions
What two monosaccharides can be degraded to a. D-ribose? b. D-arabinose? c. L-ribose?
Be sure to answer all parts.
Consider the disaccharide sophorose.
7
OH
OH
1 CH₂OH 0
sophorose
0.
3
ОН Н
ОН
15
ОН
What monosaccharides are formed when sophorose is hydrolyzed?
.
.
draw structure ...
Upper Saccharide
H
10
н
-I0-I
12 CH2OH
IO-I
Н
OH
Н
О
00 I
6
Н
I
B. Complete the following chart: (Disaccharides)
Disaccharide
Monosaccharide Subunits
Natural Source
Chapter 20 Solutions
General, Organic, & Biological Chemistry
Ch. 20.1 - Label the hemiacetal carbonthe carbon bonded to...Ch. 20.1 - Prob. 20.2PCh. 20.1 - Prob. 20.3PCh. 20.1 - Prob. 20.4PCh. 20.1 - Prob. 20.5PCh. 20.2 - Prob. 20.6PCh. 20.2 - Prob. 20.7PCh. 20.2 - Prob. 20.8PCh. 20.2 - Prob. 20.9PCh. 20.2 - Prob. 20.10P
Ch. 20.3 - Prob. 20.11PCh. 20.3 - Prob. 20.12PCh. 20.4 - Prob. 20.13PCh. 20.4 - Prob. 20.14PCh. 20.4 - Prob. 20.15PCh. 20.4 - Prob. 20.16PCh. 20.4 - Prob. 20.17PCh. 20.4 - Prob. 20.18PCh. 20.5 - Lactose contains both an acetal and a hemiacetal....Ch. 20.5 - Prob. 20.20PCh. 20.5 - Prob. 20.21PCh. 20.6 - Prob. 20.22PCh. 20.6 - Prob. 20.23PCh. 20.7 - Prob. 20.24PCh. 20.7 - Prob. 20.25PCh. 20.8 - Prob. 20.26PCh. 20 - Prob. 20.27PCh. 20 - Prob. 20.28PCh. 20 - Prob. 20.29PCh. 20 - Prob. 20.30PCh. 20 - Prob. 20.31PCh. 20 - Prob. 20.32PCh. 20 - Prob. 20.33PCh. 20 - Prob. 20.34PCh. 20 - Prob. 20.35PCh. 20 - Prob. 20.36PCh. 20 - Prob. 20.37PCh. 20 - Prob. 20.38PCh. 20 - Prob. 20.39PCh. 20 - Prob. 20.40PCh. 20 - Prob. 20.41PCh. 20 - Prob. 20.42PCh. 20 - Prob. 20.43PCh. 20 - Prob. 20.44PCh. 20 - Prob. 20.45PCh. 20 - Prob. 20.46PCh. 20 - Prob. 20.47PCh. 20 - Prob. 20.48PCh. 20 - Prob. 20.49PCh. 20 - Prob. 20.50PCh. 20 - Prob. 20.51PCh. 20 - Prob. 20.52PCh. 20 - Prob. 20.53PCh. 20 - Prob. 20.54PCh. 20 - Prob. 20.55PCh. 20 - Prob. 20.56PCh. 20 - Prob. 20.57PCh. 20 - Prob. 20.58PCh. 20 - Prob. 20.59PCh. 20 - Prob. 20.60PCh. 20 - Prob. 20.61PCh. 20 - Prob. 20.62PCh. 20 - Prob. 20.63PCh. 20 - Prob. 20.64PCh. 20 - Prob. 20.65PCh. 20 - Prob. 20.66PCh. 20 - Prob. 20.67PCh. 20 - Prob. 20.68PCh. 20 - Prob. 20.69PCh. 20 - Prob. 20.70PCh. 20 - Prob. 20.71PCh. 20 - Prob. 20.72PCh. 20 - Prob. 20.73PCh. 20 - Prob. 20.74PCh. 20 - Prob. 20.75PCh. 20 - Prob. 20.76PCh. 20 - Prob. 20.77PCh. 20 - Prob. 20.78PCh. 20 - Prob. 20.79PCh. 20 - Prob. 20.80PCh. 20 - Prob. 20.81PCh. 20 - Prob. 20.82PCh. 20 - Prob. 20.83PCh. 20 - Prob. 20.84PCh. 20 - Prob. 20.85PCh. 20 - Prob. 20.86PCh. 20 - Prob. 20.87CPCh. 20 - Prob. 20.88CP
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- What monosaccharides are formed in a modified Kiliani–Fischer synthesis starting with each of the following monosaccharides? a. D-xylose b. L-threosearrow_forwardA trisaccharide obtained from the partial hydrolysis of amylopectin showed two glycosidic linkages. A. Draw the structure of the trisaccharide B. If the trisaccharide is to be exhaustively methylated and subsequently hydrolyzed with an acid, how many different methylated products will be obtained? Draw their structures. C. Can an aqueous solution of the trisaccharide precipitate Cu as Cu2O? If it can, encircle the potential carbonyl carbon(s) in the trisaccharide. D. Can the trisaccharide exist in different anomeric forms? If yes, draw their structures.arrow_forwardFor the following trisaccharide: a. Identify its monosaccharide units, specifying the anomeric forms of of each unit present on the trisaccharide. b. What are the glycosidic bonds present on the trisaccharide? c. Is the trisaccharide a reducing sugar?arrow_forward
- 9. A trisaccharide obtained from the partial hydrolysis of amylopectin showed two glycosidic linkages. A. Draw the structure of the trisaccharide B. If the trisaccharide is to be exhaustively methylated and subsequently hydrolyzed with an acid, how many different methylated products will be obtained? Draw their structures. C. Can an aqueous solution of the trisaccharide precipitate Cu as Cu₂O? If it can, encircle the potential carbonyl carbon(s) in the trisaccharide. D. Can the trisaccharide exist in different anomeric forms? If yes, draw their structures.arrow_forward16,17arrow_forwardwhat type of bond is formed between carbon and hydrogen in each monosaccharide? a. ionic bond b. polar covalent bond c. hydrogen bond d. non-polar covalent bondarrow_forward
- Name polysaccharide which is stored in the liver of animals.arrow_forwarda. Classify this monosaccharide (e.g., aldotriose)b. Does it have the D or L configuration? c. Which carbon and oxygen become bonded in the furanose ring form of this monosaccharide (e.g., C2O6, where O6 means the oxygen on carbon 6, or "not formed")? d. Which carbon and oxygen become bonded in the pyranose ring form of this monosaccharide e.g., C2O6 or "not formed"?arrow_forwarda) Draw Haworth projections of both - and -anomers of D-fructose. Indicate which carbon is the anomeric carbon.b) Sucrose is a disaccharide made up of a molecule of D-fructose and D-glucose. Draw the structure of sucrose clearly indicating the linkage between the two monosaccharides and its biological significance.c) Tollen’s reagent is a very mild oxidizing agent which normally oxidize aldehydes but not ketones. However, both glucose and fructose give positive results with Tollen’s reagent and are classified as reducing sugars. Explain how fructose can also give positive results with Tollen’s reagent (illustrate using structures).arrow_forward
- what type of saccharide is this molecule?arrow_forwardStructures of monosaccharides are a) polymers b) pyranoses or furanoses c) aldoses or ketoses d) B and Carrow_forward- ----- -- --- . 20.45 What monosaccharides are formed when the following disaccharide is hydrolyzed? CH2OH CH,OH H. H. H O. H H. ОН НО O. OH OH OH OH H.arrow_forward
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