Draw the product of the mutarotation of the monosaccharide shown below. OH CH₂OH OH O OH H₂O* Drawing OH Atoms, Bonds and Rings Tap a node to see suggestions Charges 17 Undo Res Remove Done

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Show the cyclic rearrangement ((cyclic hemiacetal form) of the following monosaccharide. Use expanded form to show all C, H and O atoms. CH2OH HO-C-H H- OH -C-OH CH2OH O Search 13 * 12 15 17 IDI 144 2$ 4 %23 * L. 00

Which of the following best describes the disaccharide shown here? HO OH OH HO OH OH AmoH HO A. a-1,4' glycoside of D-glucose and D-galactose B. B-1,3' glycoside of D-glucose and D-galactose C. a-1,4' glycoside of D-galactose and D-glucose D. B-1,4' glycoside of D-gulose and D-galactose E. a-1,3' glycoside of D-allose and D-glucose F. a-1,3' glycoside of D-altrose and D-galactose G. a-1,3' glycoside of D-idose and D-idose H. B-1,3' glycoside of D-altrose and D-galactose O A OB OC OD OE OF OG OH F3 1-0 F4 FS MacBook Air FB

Predict the product of each monosaccharide reaction. Modify the molecule to show the product of the reaction. Atoms or bonds may need to be added or removed. 0=0 H-C-OH Н HTC OH H-C-OH H2C-OH 0=0 Н H-C-OH H-C-OH H2C-OH oxidation reduction Reaction A K Select / S С 01 Reaction B Select Draw 1 С Draw / 4 11 C C Rings 0 Н н-с HICOH н — с — Rings More H— с - он Н — он он 0 H нс — он — H- More H-C ОН с-он OH H. C ОН Erase Q2 Q О ▸ Erase 20

Name the monosaccharide below. Make sure to denote D or L and a or B. Draw the Fischer projection of the monosaccharide. (It's an aldohexose). CH2OH OH OH ОН OH

List all the reducing sugar you learnt List all the non-reducing sugars you learnt. Which of the following would be the correct classification of the carbohydrate shown below? CH₂OH H CH OH H H OH H a. monosaccharide c. polysaccharide d. starch e. cellulose O B. Amylose CH₂ C. Amylopectin -0. H OH H A) disaccharides. B) polysaccharides. C) chlorosaccharides. D) alcohol sweeteners. E) noncarbohydrate sweeteners. H OH 13. Aspartame and Saccharin® are two examples of OH Identify the polysaccharides and types of glycosidic bonds in each of the following: A. Cellulose 130 Identify the polysaccharide_ What is the glycosidic linkage? When this polysaccharide is hydrolysed in aqueous acid solution, what is formed? H 11. TEORE D 11 ANTE 114494 H CHAR -1 ( 11 CR H 11 11 11 B. Maltose ATRORE 43 18 OH 11 C. Sucrose 11 1)-( HO '11 Melibiose is a disaccharide that is 30 times sweeter than sucrose. A. What are the monosaccharide units in melibiose? D 11 03 H DIE I B. What type of glycosidic bond…

Write the product for the reduction of the following monosaccharide. (It is a hydrogenation reaction). Do not use "R" in your answer. CH2OH H- OH H -OH ČH2OH O Search 15 17 %23 %24 % & 3 4. 00 近

2. Draw the two aldohexoses and one ketohexose that can be derived from the enol shown below. HC OH но H- HO- HO ČH,OH 3. Classify the following monosaccharides as reducing and nonreducing sugars. CH,OH CH,OH CH,OH OH он но - HO- OH OH HO он OH OH ČH,OH II III 4. Identify and name the glycosidic bond in the structure shown below. CH,OH OH OH он

If the oligosaccharide shown were treated with ẞ-galactosidase, what would be the resulting products? A OH OH H OH HO- OM H OH H H H HO HO. H H OH OH two monosaccharides and one disaccharide B one monosaccharide and one trisaccharide C four monosaccharides D two disaccharides E No reaction would occur. H HO OH H OH