Concept explainers
a)
Interpretation:
Fischer projection of D-sugars are to be drawn.
Concept introduction:
Fischer Projections are typically used for depicting monosaccharides and amino acids. They are helpful with depicting monosaccharides, because they have so many stereocenters, and the different monosaccharides are all pretty similar, they are just different about the orientation of the stereocenters. The Fischer Projection allows us to quickly see the orientation of each monosaccharide.
b)
Interpretation:
Fischer projection of D-sugars are to be drawn.
Concept introduction:
Fischer Projections are typically used for depicting monosaccharides and amino acids. They are helpful with depicting monosaccharides, because they have so many stereocenters, and the different monosaccharides are all pretty similar, they are just different about the orientation of the stereocenters. The Fischer Projection allows us to quickly see the orientation of each monosaccharide.
c)
Interpretation:
Fischer projection of D-sugars are to be drawn.
Concept introduction:
Fischer Projections are typically used for depicting monosaccharides and amino acids. They are helpful with depicting monosaccharides, because they have so many stereocenters, and the different monosaccharides are all pretty similar, they are just different about the orientation of the stereocenters. The Fischer Projection allows us to quickly see the orientation of each monosaccharide.
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Organic Chemistry
- 6 сH-он (5 4 OH 1 2 ОН 3 OH (c) Trace and identify the acetal in the above monosaccharide. (d) Draw the hemiacetal that results from above acetal. (e) Draw the open chain equivalent of the sugar in part (d).arrow_forwardD-Tagatose is epimeric of D-Fructose at C4. What is the structure of α-D-Tagatofuranose?arrow_forwardWhich of the following statements about the monosaccharide shown below is correct?arrow_forward
- .. Draw Haworth projections for the following: (a) CHO in a-furanose form. Name the sugar. H-C- OH но-с—н H-C-OH CH,OH (b) The L isomer of (a) (c) a-D-GlcNAc (d) (d) a-D-Fructofuranosearrow_forwardatching an a 1,4 linkage a ẞ-1,4 linkage a nonreducing monosaccharide a reducing sugar a reducing disaccharide a deoxy sugar (A) (c) он CH₂OH (E) 1107 CHOH CHOH CH₂OH CH₂OH CHOH CH₂OH он On но- OF CHLOH HO Lot HO OH CH₂OH HO HOCH OH (F) OH (0)arrow_forward23-58 Predict Hhe poducts obtained when D-fruitose reacts with each reagent. x) No BHy (Y) Ag(NiHa), OH- (2) excess Ch,I, Ag20arrow_forward
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- Give detailed Solution with explanation needed..don't give Handwritten answer..don't use Ai for answering thisarrow_forwardDraw the Haworth or Chair Haworth structures of the following disaccharides: (a) α-D-glucopyranosyl-(1,4)-β, D-galactopyranose (b) β,D-galactopyranosyl-(1,4)-α-D-glucopyranose (c) β-D-glucopyranosyl-(1,4)-α,D-galactopyranose. Identify all anomeric carbons and hemiacetal, acetal, hemiketal, and ketal linkages.arrow_forwardusing the picture below as reference: do the following: a.) label if any of the structures (A-D) are any of these classes of compounds: - a keto-pentose - an L-monosaccharide - a hexose b.) then draw the Haworth projections of compound A as an α-isomerarrow_forward
- Introduction to General, Organic and BiochemistryChemistryISBN:9781285869759Author:Frederick A. Bettelheim, William H. Brown, Mary K. Campbell, Shawn O. Farrell, Omar TorresPublisher:Cengage Learning