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- The synthetic process by which monomers are covalently linked is (a) hydrolysis (b) isomerization (c) condensation (d) glycosidic linkage (e) ester linkageD-Glucose and D-Galactose are A H D C=0 H-C-OH OH C-H H-C-OH H_C-OH CH₂OH D-Glucose ketoses epimers pentoses enantiomers H ... н-с-он OH-C-H он-с-н H-OH CH₂OH D-GalactoseThe functional group represented by N2 is: Amide Amine Lactone Lactam
- Which of the following is true regarding Glycogen Linear homopolysaccharide O Contains beta-1 to 4 bonds O It has alph-helical structure O Energy storage heteropolysaccharide O Branched heteropolysaccharideWhich of the following shorthand names best characterizes the following disaccharide? CHOH OH H. он H. H. OH Glc (a1-4)Gal Gal (a1-4)Glc O Glc (B1-4)Gal Gal (P1-4)GlcWhich of the following best describes the glycosidic bond in the disaccharide shown? CHOH CHOH CHOH OH OH он Он a(1-4) B(1-4) a(2-4) B(2-4)
- Which of the following disaccharides below is not a reducing sugar?Indicate whether each of the following monosaccharides would be classified as an aldose, ketose, triose, tetrose, pentose, or hexose (each can be classified into two different categories). Which of these sugars would exist predominantly in the cyclic form?Describe the important biochemical properties of carbohydrates and why carbohydrates would be considered polar molecules. A▾ B I X @ F 7
- A reducing sugar will undergo the Fehling reaction, which requires a(potential) free aldehyde group. Which of the disaccharides shown inFigure are reducing and which are nonreducing?In the following monosaccharide hemiacetal, identify the anomeric carbon atom. Identify the appropriate atom by selecting an atom and assigning it a map number of 1. To do this, rigl mark to enable the Map field before entering a value. H: 122 EXP" CONT. 0 0 H но OH S Br OH [1] ÓH P. -Draw the structure and give the name of the epimers of the following monosaccharides ALDOTRIOSE CHO Carton taamber HOOH 3 CH,OH Dlilyeeraldehyde CHO 2 HCOH Carbon number ALDOTETROSES HCOH нон D-Erythrose CHO CHO HOCH HCOH Carbon uumbes HOOH HXOH SISOINIJOTTV HOOH HCOH CHOH CHLOH Arabinose (Ara) nXylose (Xyt) CHO CHO CHO CHO 2 HCOH HCOH HCOH HOCH 3 HCOH HOCH HCOH HOCH Carbon TRmber 1 HCOH HCOH HOCH HOCH 5 HOOH HCOH HCOH HCOH CHOH CHOH CHOH CHOH THGlucose (Gle) Allese -Gulose Talose ALDOHENOSES