Draw the monosaccharide that results when structure I is treated with HNO3. Is theresulting product optically active?Structuresandare enantiomers.Structuresandare a pair of epimers.Structuresandare another pair of diastereomers. CHOCHOCHOCHOCHOно-H-H--Он ноH-OHH-HO-H-HO-но-H-OH HOНоноH-но-OHH-НоH-OHно-Ноно-H-HO-ČH2OHCH2OHCH2OHCH2OHČH,OHIIIIIIIVV

Carbohydrates contain multiple stereocenters and hence many isomers are possible. So such compounds…

Answered: Draw the monosaccharide that results…

Biochemistry

9th Edition

ISBN:9781319114671

Author:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Publisher:Lubert Stryer, Jeremy M. Berg, John L. Tymoczko, Gregory J. Gatto Jr.

Chapter1: Biochemistry: An Evolving Science

Section: Chapter Questions

Problem 1P

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Listed below are descriptions that may belong to amylose, amylopectin, both, or it may not belong to either. Write A if it describes amylose, B if it describes amylopectin, AB if the statement applies to both, or O if it doesn’t apply to either. 1. Its monosaccharides are bound by at least one α-1,4-glycosidic bond. 2. It contains α-1,6-glycosidic bonds. 3. It can be broken down by the enzyme α-amylase. 4. A polysaccharide made up of gulose. 5. It can form a double helix.
Please note the image question below. CH₂OH ç-o CH₂OPO Dihydroxyacetone phosphate triose phosphate isomerase O True O False H HCOH CH₂OPO Glyceraldehyde 3-phosphate This is a change in configuration because isomers can only be interconverted by temporarily breaking covalent bonds.
Assign a name to each of the following monosaccharides. Use D and L designations. H b. CH 2OH a. C=0 C=0 HO-C-H H-C-OH HO-C-H Н-С-Он CH,OH CH 2OH a. b. Circle all chiral centers for the monosaccharides shown. С. d. True or False: The molecules shown can rotate plane polarized light?
Modify the mannose structures provided to show the structure of a disaccharide formed from two mannose units joined by a 1. →>> • 6-B-glycosidic linkage. Снон Н Он H Он H Н ОН Он ОН Он Он H Он H H H Н Н
The monosaccharides shown below are: a Diastereomers b Enantiomers c Epimers d Anomers
Draw the structure of the product that forms when the carbonyl compound shown is treated with K2Cr2O7. If no reaction occurs, draw the structure of the organic starting material (reactant). CHO
For Gal(Beta 1 - 4)Glc, Explain in detail the glycoside bond: What carbon involved in glycoside bond? What isomerization? Also, What anomeric still free?
Which of the following differentiates chitin with cellulose? Chitin has the alpha (1-4) glycosidic linkage O Chitin has an amino derivative of glucose O Chitin is a polysaccharide and cellulose is a disaccharide Chitin has the beta (1-4) glycosidic linkage.
A) Refer to the figure below, Identify and explain the two types of reactions, and describe what are the importance of these reactions to our bodies. Reaction 1 H Monomer Reaction 2 H H OH + H H H₂O H H₂O OH + H H OH OH + H H₂O H₂O OH OH + H OH OH OH OH B) What are the main chemical interactions that determine and maintain the quaternary structure of proteins. Also, what are the conditions that can alter these interactions? [
Classify each of the following molecular formulas as an acyclic alkane or a cycloalkane. Part 1 of 4 CH: (Choose one) Part 2 of 4 C17H34 (Choose one) Part 3 of 4 C21H44 (Choose one) Part 4 of 4 C22H46 (Choose one) x X
Identify the structures shown as glycerophospholipids or sphingolipids.
Describe the important biochemical properties of carbohydrates and why carbohydrates would be considered polar molecules. A▾ B I X @ F 7

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Draw the monosaccharide that results when structure I is treated with HNO3. Is th resulting product optically active? Structures and are enantiomers. Structures and are a pair of epimers. Structures and are another pair of diastereomers.