a) Use the carbonyl group, number of carbons, and type of stereochemistry (D or L) toclassify the following monosaccharides.CH2OHO:CHOIно-H-HO-но-H-HOCH2HO--O-CH2OHH-OHCH2OHi.Compound A is a(nwithstereochemistry.ii.Compound B is a(n)withstereochemistry.

Introduction: Stereochemistry is a branch of chemistry that is based on the three-dimensional…

Answered: a) Use the carbonyl group, number of…

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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An incomplete structure of a porphyrin ring is shown below. The structure is missing three pi bonds and does not show the non-zero formal charges on two atoms. Complete the structure of the porphyrin ring with the missing pi bonds and formal charges. 0 0 +t DC 12⁰ H C N O S F P Cl Br I
CH;OH НО OH What is the name of this structure? OH OH alpha-D-gulopryranose O beta-L-gulofuransone O alpha-L-gulofuranose beta-D- gulopyranose
Indicate next to each letter the name of the monomers shown below and write the name of the polymer that is produced from the monomer. H-C-OH HỌ-C-H H-C-OH H-C-OH о- 6 CH₂OH 0=P-O О CH₂ Phosphate H group А: Name of polymer: H- Н Н OH H Sugar Н Н. H Nitrogenous base (adenine) C: 0 НО Name of polymer: H C-C-N CH2 SH Н НИ Н III H-N-С-С-0 +111 НКН н B: Name of polymer: Н 0 0-C-H o Н-С-0² H-C-O H S ННННННННННН Н Н Н LI -CH Н ННННННННННН Н Н Н ITIILE I C-C H ...... С-с-с-с-с-с-с III E .. ННННННННННН Н Н С-С-f 111 1 FE D: I НННННННННННННН No polymer!
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
Classify the following lipid (choose all that apply).CHOOSE ALL THAT APPLY a. monounsaturated b. omega-6 c. triglyceride d. saturated e. steroid f. polyunsaturated g. omega-3 h. wax ester i. fatty acid
Choose the correct structure for thiamine hydrochloride at pH 10. H3C H3C N NH₂ NH₂ CI- A CI- с CH3 CH3 HCI -OH OO H3C H3C N NH3 NH₂ CI- B D CH3 S CH3 S HCI OH -OH
6. The [a] of cheatalotic acid is + 10°. The structure shown below was thought to be correct. Answer for Part b HO, COOH H, HO OH Cheatalotic Acid Incorrect Structure a) Why is the structure shown incorrect? b) Propose a cture of cheatalotic acid that can possibly be correct, assuming atom connectivity is correc
Identify the names of the following molecules.
Which of the following organic compound doesnot dissolve in water? glycerol propane propanoic acid propanol H H-C Н Н H-с-с-с Н- OH HICIH H-C c-c 1 Н OH H -+ Н HICIH H Н H H C C H H OH 5-о-т OH -C-H -H OH
How many stereoisomers are possible for the following monosaccharide? a. 4 b. 8 c. 16 d. 2 e. 1
1) How many different forms of D-monosaccharide are present at equilibrium in an aqueous solution? a) 4 b) 2 c) 1 d) 3
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

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a) Use the carbonyl group, number of carbons, and type of stereochemistry (D or L) t classify the following monosaccharides. B CH2OH 0: CHO но -H- HO- Но -H- HOCH2- -HO- HO- ČH,OH ČH2OH i.Compound A is a(n with stereochemistry. ii.Compound B is a(n) with stereochemistry.