Please draw all four bonds at chiral centers. Use wedge and dash bonds at chiral centers only. Do not use wedges and dashes at non-chiral centers.Edit the structure below to draw its enantiomer.CCH3ChainSFCIBr14 OF 25 QUESTIONS COMPLETED< 18/25 >• SUBMIT ANSWER erization 2Edit the structure below to draw one of its diastereomers.CH3H.14 OF 25 QUESTIONS COMPLETED

Enantiomers are the compounds that are mirror image to each other but are not superimposable .

Answered: Please draw all four bonds at chiral…

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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Consider this monosaccharide. H H OH H .OH HO H HO H CH₂OH Part: 0/3 Part 1 of 3 Label the chirality center(s) for the monosaccharide by highlighting the carbon(s) in the structure below. H H -OH H -OH HO -H HO -H CH₂OH હે
Give the IUPAC name for each compound. Part 1 of 2 2-methylhept-3-ene n ☑ Part 2 of 2
1. (a) The diagram below shows a structure of monosaccharide. CH,OH C=0 H-C-OH НО—С—Н ČH,OH i. Draw the figure above on your answer sheet and indicate ALL chiral carbon(s) in your figure with *. ii. With reference to the number of carbon, the type of carbonyl group and D/L configuration, suggest a name consisting these three properties to describe the monosaccharide shown above. Explain why this monosaccharide is in D- or L- configuration as you suggested in (ii). 111. (b) The diagram below shows different configurations of glucose. CH,OH CHO ÇH,OH H H-C-OH O. OH H. H. OH H. H OH HO-C-H но H-C-OH но H. H-C-OH OH OH ČH,OH A В C i. Which glucose molecule, A or C, is in a configuration? Explain. ii. What is the name of the conversion among different configurations? iii. Glycosaminoglycans (GAG) consist of modified sugars. Give a name of the typical modification to the sugar. What makes GAG ideal for the fluid in the joints? to
how do we name the bond between monomer B and monomer C？（anomeric designation‘s name plesse）
Consider these three monosaccharides. H H CH₂OH H- -OH HO H HO H H -OH H OH CH₂OH CH₂OH CH₂OH Part 1 of 3 Which two monosaccharides are stereoisomers? Check two. HO H H OH CH₂OH H -OH H OH CH₂OH CH,OH HO -H снон None of the above Part 2 of 3 Identify two compounds that are constitutional isomers. Check two. CH,OH C=0 Undo HO -H HO H CH,OH H OH CH₂OH H -OH H .OH CH₂OH None of the above Part 3 of 3 Use the Fischer projection carbon drawing tool to draw the enantiomer of this monosaccharide. H H -OH H -OH CH₂OH Click and drag to start drawing a structure.
Consider the following cyclic monosaccharide. CH₂OH H H H H OH HO OH Part 1 of 2 OH H Classify the monosaccharide as an aor ẞ isomer. Select the single best answer. ○ẞ isomer a isomer Part: 1/2 Part 2 of 2 Draw the other isomer of the cyclic form using a Haworth projection. Click and drag to start drawing a structure. ם' G
Consider the structure shown below. он 3 5 CH; O CH, O H CH; O 1 H-N-CH,-C-N-CH;-C-N-CH-C-N-CH-C-N-CH-C-ơ 2 H. H H Fill in the blank with an integer (1, 2, 3, 4, 5..) as shown in the diagram or to represent a specified number. A hydrophilic side chain is indicated by the number
U Below are three hypothetical reaction intermediates: 2 CH3 CH3 C=0- C=0- H-C- H-C-H H-C- Н 3 CH3 -C=0 Note the carbanion on each intermediate. Which of the following are true? (Pick two.) Compound 1 is the lowest energy of the three intermediates. Compound 2 is the lowest energy of the three intermediates. Compound 3 is the lowest energy of the three intermediates. Resonance with the carbonyl oxygen (arrow) stabilizes the carbanion shown on compound 1 Resonance with the carbonyl oxygen (arrow) stabilizes the carbanion shown on compound 2
cis, cis-9,12-OCTAdecadiENoic acid Enumerate the number of carbons and unsaturations (double bonds) in this molecule
Hhhh

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Please draw all four bonds at chiral centers. Use wedge and dash bonds at chiral centers only. Do not use wedges and dashes at non- chiral centers. Edit the structure below to draw its enantiomer. Chain C CH3 S F P CI Br H