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Chemistry
10th Edition
ISBN: 9781305957404
Author: Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher: Cengage Learning
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Which of the following glycosidic linkage is found in maltose?
a. Glucose (α1 – 2β) Fructose
b. Glucose (β1 – 4) Glucose
c. Galactose (β1 – 4) Glucose
d. Glucose (α1 – 4) Glucose
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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_forwardD- 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 Endarrow_forward7. 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 Glucosearrow_forward
- Draw chair configurationarrow_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_forwardFor each of the following disaccharides, circle the glycosidic linkage and indicate the type ofglycosidic linkage:arrow_forward
- For each of the following disaccharides, circle the glycosidic linkage and indicate the type of glycosidic linkage:arrow_forwardWhich of the following types of monosaccharides have cyclic forms that involve a 5-membered ring? a. Aldohexoses and ketopentoses b. Aldopentoses and ketopentoses c. Aldopentoses and ketohexoses d. All of the above.arrow_forwardThe following two monosaccharides are what type of isomer? CHO CHO H- H- OH HO H. HO H. HO H- H OH OH CH,OH ČH,OH O a. anomers O b. ionomers O c. diastereomers O d. enantiomer O e. structural isomers Jump to.arrow_forward
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