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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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
Transcribed Image Text:The image shows a chemical structure of "Gentiobiose." It consists of two glucose molecules linked together. The structure depicts the hydroxyl groups (OH) and the glycosidic linkage between the glucose units.
Below the diagram is a question labeled "Part A":
"What simple sugars do you obtain on hydrolysis of gentiobiose?"
The options provided are:
1. α-D-Glucose and α-D-Glucose
2. β-D-Fructose and β-D-Fructose
3. α-D-Glucose and β-D-Glucose
4. β-D-Fructose and α-D-Fructose
There are buttons for submitting and requesting answers, suggesting it is part of an online quiz or exercise.
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- What is the relationship between these two sugars? H- HO HO CH₂OH OH ∙H -H CH₂OH A) identical structures B) enantiomers C) diastereomers D) constitutional isomers E) non-isomeric H- H- H- CH₂OH -OH -OH -OH CH₂OHarrow_forwardAt which carbon are the following sugars epimers of each other? O=CH H―OH HO-H O=CH H-OH HO-H HO-H H- -OH HOH H- -OH CH₂OH CH₂OH Ο O C-1 C-2 C-3 C-4 C-5arrow_forwardThe Products of the reaction of L-glucose with the following L-glucose [1] NH2NH4 [2] Ac20,NaOAc [3] NaOCH3arrow_forward
- Which of the following is a reducing sugar? HO но OH но но HO" "OH HO" "OH Он но OH он HO A D A В Carrow_forwardDraw the cyclic alpha equivalent of the sugar shown belowarrow_forwardName the following carbohydrate: H 0. H-C-OH │ HO C H H-C-OH H-C-OH CH2OH Aldohexose Ketohexose Aldopentose O Ketopentosearrow_forward
- Given the following sugars: If sugar D were to undergo Ruff degradation once, what would be the product? When reacted with HNO3, which sugar will form an optically inactive product?arrow_forwardClassify each of the following compounds as reducing or non-reducing sugars. Please be very clear in your explanation.arrow_forwardWhat is the relationship between the following monosaccharides? O= HO HO-H Но H H +OH -HO- ОН HO-H Но OH OH CH2OH CH2OH diastereomers completely different epimers enantiomers エエ エエarrow_forward
- The sugars can be classified as either aldoses or ketoses. Classify each structure with the correct name. НО НО H Н CHO —H -H -OH -OH CH₂OH НО НО Н CH₂OH c=0 H -н -OH CH₂OH НО НО н CHO ketose -H -Н OH CH₂OH Answer Bank aldose CHO H-C-OH CH₂OH НО Н CH₂OH c=0 -Н -OH CH₂OH " CH2OH O CH2OHarrow_forwardIf 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 OHarrow_forwardWhat is the name of the sugar shown here? HO OH OL-xylose O D-xylose O D-erythrose OL-erythrose O D-threose O L-threose Oll.arrow_forward
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