
Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Convert each Haworth projection to an open-chain form and then to a Fischer projection. Name the monosaccharide you have drawn.

Transcribed Image Text:CH,OH
H
H
ОН
H
НО
H
ÓH ÓH
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- 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 OHarrow_forwardCompare the following monosaccharides and choose the best description. a. same sugar b. enantiomers c. diastereomers d. different sugarsarrow_forwardMark the TRUE alternative regarding the following trisaccharide: a) It has two glycosidic bonds. b) It has reducing power. c) All the monosaccharides that constitute it are glucose units. d) It has three glycosidic bonds. e) It presents mutarotation.arrow_forward
- Assign a name to the following monosaccharide. Use D and Ldesignation. CHO HO H HO H Но- HOH ČH2OHarrow_forwardClick the "draw structure" button to launch the drawing utility. Consider the following monosaccharide. H draw structure ... HO- -C-H HO–C—H HO- -C-H H-C-OH CH₂OH Draw the a anomer of the cyclic form.arrow_forwardDraw the open-chain Fischer projection of the monosaccharide pictured. Provide the classification name for this monosaccharide and label each stereocenter as R or S. Use the key as a reference.arrow_forward
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