Please refer to the monosaccharides below when answering questions (a) – (j). CHO CHO СНО CHO CHO Но H- Но Но H- ОН H- HO- Но H- H- ОН НО H- OH Но -H- H- -HO- Но H- H OH HO- H- HỌ H- H- -HO- Но -H- НО H- Но- H- CH2OH CH2OH ČH,OH CH2OH CH2OH I II III IV V (a) Draw the monosaccharide that results when III is treated with Br2/H2O. (b) Draw the monosaccharide that results when III is treated with 1. NaBH4/ 2. H2O. (c) Draw the monosaccharide that results when II is treated with the following reagents: 1. Br2/H2O 2. Cа(ОН)2 3. H2O2/Fe3+

a) Which of the following monosaccharides will react with Tollens' reagent? Circle all that apply. СООН CH2OH CH2OH OCH3 но- H- O: OH но H- но—н OH ČH2OH ČH2OH ÓH II III IV V b) Which of the following carbohydrates is sucrose? OH OH OH но OH HO, O. OH "OH HO OH Он HO OH II I HO, HO. Он HO, HO. HO, OH Но Он но. OH HO,, HO, OH HOl HO OH но он III Он HO IV HO но

Please draw a tetrasaccharide. The cyclic monosaccharide needed is pictured below. Step 1: Connect 3 glucose units through a (1-4) glycoside bonds Step 2: Connect the 4th glucose unit to the second glucose unit through a a (1-3) glycoside bond glucose CH₂OH OH OH OH OH

D- and L- designations are used to distinguish between the two possible enantiomers of the monosaccharide, fructose. From the Fischer projection, determine the designation of this monosaccharide. CH,OH A) D B) L H- HO. C) D, L Но- -- D) This monoşiaccharide contains no chiral centers. но -- CH2OH W Type here to search PgUp F11 DII PrtScn Home End

7. Draw the Haworth structure for the following monosaccharides a. H НО H c=0 H + но - н 3 4 Н 5 - ОН - OH 애 CH₂OH 6 D-Mannose b. H 0 = с H - C - OH HO-C - H H - C - OH H - C - ОН CH₂OH Glucose

Select the glycoside(s) that are formed when the following monosaccharide is treated with CH3CH₂OH, HCI. HO OH OH HO- НО. OH OCH₂CH₂ OH OH OH OCH₂CH₂ OH OH OH -OH HO OH OH OH С HO- OH CH3CH₂OH HCI OH OH OCH₂CH3 -OCH₂CH3 a НО НО OH OH OH OH OH OCH₂CH₂ OCH₂CH₂ Lo -OH HO OCH CH НО. OH OH -0 OH OCH₂CH₂ OH -OH OCH₂CH₂

A disaccharide is shown below. For part (a), circle the anomeric carbon atoms. For part (b), explain whether it is a reducing sugar or non-reducing sugar.

Provide the systematic name of the cyclic monosaccharide shown here Be sure to include the structural form as a component of the name. H Question 78 of 95 OH CH₂OH H OH H mann H OH O B- D- a- L- fruct gluc pyran furan galact ose oside ol OH H

(g) Using appropriate prefixes/infixes/suffixes (ketoheptose, aldoheptose, etc.), classify each of the monosaccharides shown below. CHO CH2OH Но IH но- HO- HO- HO H. CH2OH CH2OH I II (h) Identify B-D-altrose and a-D-altrose from the monosaccharides shown below. CH2OH CH2OH CH2OH CH2OH OH OH OH ОН OH ОН ОН OH OH OH OH OH OH OH OH OH I II II IV (i) Identify B-D-altrose and a-D-altrose from the monosaccharides shown below. VI I CH2OH O CH2OH II H V ОН, III IV OH OH H

Hello! I am working on a practice assignment for an upcoming exam. I have already completed both parts of this question but I am hoping to check my work. Please be clear in your explanations I'm really trying to make sure I understand everything.   Thank you!