Exam 21: Biomolecules: Carbohydrates
Exam 1: Structure and Bonding30 Questions
Exam 2: Polar Covalent Bonds: Acids and Bases35 Questions
Exam 3: Organic Compounds: Alkanes and Their Stereochemistry32 Questions
Exam 4: Organic Compounds: Cycloalkanes and Their Stereochemistry18 Questions
Exam 5: Stereochemistry at Tetrahedral Centers33 Questions
Exam 6: An Overview of Organic Reactions32 Questions
Exam 7: Alkenes and Alkynes34 Questions
Exam 8: Reactions of Alkenes and Alkynes37 Questions
Exam 9: Aromatic Compounds36 Questions
Exam 10: Structure Determination: Mass Spectrometry,infrared Spectroscopy,and Ultraviolet Spectroscopy41 Questions
Exam 11: Structure Determination: Nuclear Magnetic Resonance Spectroscopy37 Questions
Exam 12: Organohalides: Nucleophilic Substitutions and Eliminations37 Questions
Exam 13: Alcohols,phenols,and Thiols: Ethers and Sulfides19 Questions
Exam 14: Aldehydes and Ketones: Nucleophilic Addition Reactions30 Questions
Exam 15: Carboxylic Acids and Nitriles23 Questions
Exam 16: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions42 Questions
Exam 17: Carbonyl Alpha-Substitution and Condensation Reactions84 Questions
Exam 18: Amines and Heterocycles28 Questions
Exam 19: Biomolecules: Amino Acids,peptides,and Proteins36 Questions
Exam 20: Amino Acid Metabolism34 Questions
Exam 21: Biomolecules: Carbohydrates42 Questions
Exam 22: Carbohydrate Metabolism41 Questions
Exam 23: Biomolecules: Lipids and Their Metabolism31 Questions
Exam 24: Biomolecules: Nucleic Acids and Their Metabolism23 Questions
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Using the following structure of D-talose as a guide,draw the structure for a-D-talopyranose.Label each ring substituent as axial or equatorial.
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Aldohexoses may exist as furanoses or pyranoses.Aldopentoses also may exist as furanoses or pyranoses.

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Instructions: Refer to D-iodose below to answer the following question(s).
Refer to instructions.The Fischer projection for D-iodose (above)corresponds to which pyranose below?
(Multiple Choice)
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Use the information below to answer the following questions.
a) Which of the above represent an aldose?
a. only 1 and 2
b. only 1 and 3
c. only 2 and 3
d. 1, 2 and 3
b) Which of the above would not be oxidized by an aqueous solution of Br2?
a. only 1
b. only 2
c. only 3
d. all of these
(Short Answer)
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Instructions: Refer to the monosaccharides below to answer the following question(s).
-Refer to instructions.Assign R or S configuration to each chirality center in sorbose.
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Instructions: Refer to the equilibrium below to answer the following question(s).
Refer to instructions.The correct name for the cyclic structure is____.
(Multiple Choice)
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Convert the following Fisher projections into tetrahedral representations.
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Which reagent would be best suited for the transformation shown? 
(Multiple Choice)
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What is the relationship between D-erythrose and D-threose? 
(Multiple Choice)
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Instructions: Refer to the monosaccharides below to answer the following question(s).
-Refer to instructions.Draw both chair conformations of the a-anomer of rhamnose in its pyranose form.Circle the more stable conformation.
(Essay)
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Instructions: Refer to the sugars below to answer the following question(s).Choose the sugar that best fits each description.There is only one correct answer for each question,but sugars may be used more than once.Indicate each answer by the corresponding letter.
-Refer to instructions._____ a dextrorotary hexose and ______ a levorototary tetrose.
(Multiple Choice)
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Instructions: Refer to the monosaccharides below to answer the following question(s).Classify each sugar by type;for example,glucose is an aldohexose.
-Refer to instructions.Sorbose is ____________________.
(Short Answer)
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If the following compound undergoes oxidation in the presence of the appropriate enzyme,draw the structure of the likely product.
(Essay)
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Instructions: Refer to the monosaccharides below to answer the following question(s).
-Refer to instructions.Provide the complete name for the a-anomer of rhamnose in its pyranose form.
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Instructions: Consider the reaction below to answer the following question(s).
-Refer to instructions.Place a triangle around the anomeric carbon in compound Q.
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Instructions: Consider the reaction below to answer the following question(s).
-Refer to instructions.Which anomer is the LEAST stable?
Q or Z
(Short Answer)
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