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Name the following monosaccharide: H H OH H OH HO H H OH O aldopentose O...
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keloletrose aldotriose O ketotriose O aldopentose O ketopentose O aldotetrose CHO H-OH CH OH O aldotetrose O ketohexose O ketotetrose O ketopentose O aldopentose O aldohexose CH-OH OH 0 OH OH OH O aldohexose kelotetrose O ketohexose O ketopentose O aldotetrose O aldopentose fructose Previous Give Up & View s
Classify each monosaccharide in terms of functional group and
number of carbon atoms.
a. HOCH CHC-H OH 0 Ketotetrose 0 Ketopentose 0 O Aldopentose 0 Aldotetrose 0 Ketohexose 0 Ketotriose O Aldotriose O Aldohexose b. HOCH,CHỨCH,OH OH O Ketotetrose O Ketotriose O Ketopentose O Aldotetrose O Ketohexose O Aldopentose O Aldotriose O Aldohexose OOH C. HOCH,CCHCHCHCH,OH ОН ОН 0 Ketopentose Aldotriose Aldotetrose O Aldohexose 0 Ketotriose O Aldopentose o Ketotetrose Ketohexose o OH d. H-CCHCHCH2OH OH O Aldotetrose 0 Ketotetrose...
Question 8 H-C-OH H-C-OH - OH CH, OH Select the right name of this carbohydrate sturcture A. ketopentose B. aldohexose C. aldopentose D. aldotetrose
Question 2 of 33 > Classify the monosaccharides according to the position of the carbonyl group and the number of carbon atoms in the molecule. Сн,он CHO —н но O OH ону H- -он OH CH OH OH O aldopentose ketotriose ketotetrose ketohexose ketopentose ketotetrose aldohexose aldopentose aldotetrose O O ketopentose O aldotetrose aldotriose O CH2OH OH 0 < HO CH OH OH O aldotetrose O aldohexose O ketohexose O aldopentose O ketopentose Oketotetrose
Classify each of the following monosaccharides by the type of
carbonyl group and the number of carbons (for example, a
monosaccharide with an aldehyde and three carbons is an
aldotriose).
ketotriose aldohexose CH2OH CH2OH aldotetrose 이 H CH OH ketotetrose I 운 우 ketopentose HH H1 ketohexose CHOH CH2OH aldopentose aldotriose
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The following monosaccharide is classified as alan ОН НОН,С о Ho/cн,он ОН A. aldohexose B. aldopentose C. ketohexose D. ketopentose
C=O 2. Which of the following is an example of an aldopentose? Circle your answer. СН,ОН CH,он CH н-с-он H-6-H H-C-OH HO-C-H. H-C-H H-C-OH H-C-OH H-6-H H-C-OH CH,OH CH,OH CH OH 3. In the L- isomer of a Fischer projection of a monosaccharide, the -OH group furthest from the carbonyl is written. Circle your answer. on the left of the top chiral carbon. on the left of the middle chiral carbon. on the left of the bottom chiral carbon. on...
its a two part question use the first question to answer the
second one
Correctly assign R or S to the carbons labeled a) 2 and b) 5. СНО HO- 2H HOTH H- OH н 5-ОН CH,OH 1. The structure in Q10 is an example of a: a) L-aldohexose b) D-aldohexose c) L-ketohexose d) D-ketohexose e) L-aldopentose f) D-ketopentose
Which of the following is the correct classification of the
carbohydrate
Aldoheptose
Aldohexose
Aldopentose
Ketoheptose
Ketohexose
Ketopentose
2. When glucose is coverted to sorbitol by an Aldose
reductase. What type of reaction occurs when NAPH is converted to
NADP+
Substitution
Proton transfer
Oxidation
Reduction
Rearrangement
3 Why is alkyl litium (RLi) a bond and not unshared
pairs?
HO HO O H O H H H H H OH OH OH OH OH H OH cs a) Circle the glycosidic bond. b) Identify the type of glycosidic bond that is present in this molecule. c) What type of molecule is this? I- H