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The Haworth structure of sophorose, a carbohydrate found in beans, is shown below. (5 pts) a...
What elements make up a carbohydrate? What ratio are these always found in? molecules that combine...
What elements make up a carbohydrate? What ratio are these always found in? molecules that combine to form maltose (draw What is a disaccharide? Draw the reaction of two glucose the structures) function of starch, cellulose, and glycogen. What are polysaccharides? Describe the structure and Study the diagrams below, which show carbohydrate molecules. Beside each molecule, write whether it is a monosaccharide, a disaccharide, or a polysaccharide. он CH OH H HOCH но он н нон Glucose он н CH2OH...
S he structure of sucrose ( 7) (4 pol (table Sugar) lactulose is shown below. Decide for each of ...
s he structure of sucrose ( 7) (4 pol (table Sugar) lactulose is shown below. Decide for each of the statements Label the glucose and fructose rings below whether it is True or False. нон он This ring is This ring is H2OH (T or F) Sucrose contains two acetal linkaes and no hemiacetal linkage. A. B. (T or F) Sucrose is a reducing sugar. C. (Tor F) Sucrose does not undergo mutarotation. D. (T or F) The glycosidic linkage...
need help! 21. The following sugars condense to form an α(1-4) glyosidic bond. Using the Haworth...
need help!
21. The following sugars condense to form an α(1-4) glyosidic bond. Using the Haworth templates below, neatly number the carbons and draw in the new glycosidic bond OH он но H OH H OH 22. When fructose cyclizes, it forms a hemiacetal. Complete the structure for the a-fructose anomer CH2OH HO OH он CH2OH D-fructose Chem 1050 Exam 2 review problems 23. What are the products when the following two molecules undergo a condensation? 24. What are the...
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose....
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if a di- or polysaccharide (e.g., B,B-2,3; if there is more than one glycosidic bond, draw an arrow from each label to its corresponding bond). CH,OH CH2OH CH OН но н H Н H Он Н OH н OH Он Н ОН O H Но он b. a. OH H OH CH-OH O H Но ОН Н CH2OH CH2 CH2OH он OCH CH3 Но н...
y/node/845/take/3 Question 3 Classify the glycosidic linkage #3 in the structure shown below. Your answer must...
y/node/845/take/3 Question 3 Classify the glycosidic linkage #3 in the structure shown below. Your answer must be in the form: type-#,# For example, alpha-2,3 or beta-4,6 Cн-он O H Hi H он HO H # 4 O H OH [X] CH2 O H HA CH, он сн,он CH,OH # 3 OH OH O H H H # 2 H H OH OH OH Hi OH но H OH # 1 H OH [W) H. H OH OH Answer Enter your...
18. Which of the following compound(s) would undergo mutarotation in aqueous solution? 19. Draw the chair...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
1a-h Chapters 21 and 22: 14 1. Consider the structure shown on the right and answer...
1a-h
Chapters 21 and 22: 14 1. Consider the structure shown on the right and answer the following (4 questions about it (fill in blanks or circle proper choice). a. Its molecular formula is C H O and so it fits the general formula for a carbohydrate, which is Ca b. Specifically, this structure is (a D/ an L) (aldo/keto) (pent/hex) (ase/ose). c. Will it be optically active?_ d. If the top carbon was converted to a CH,OH, would it...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...
Chapters 21 and 22: 1. Consider the structure shown on the right and answer the following questio...
Chapters 21 and 22: 1. Consider the structure shown on the right and answer the following questions about it (ill in blanks or cirele proper choice) (4 a. Its molecular formula is G ,H( )0( , and so it fits the CHOH , general formula for a carbohydrate, which is b. Specifically, this structure is (a D/ an L) (aldo/keto) (pent/hex) (aselose) c. Will it be optically active? d. If the top carbon was converted to a CH,OH, would it...
What elements make up a carbohydrate? What ratio are these always found in? molecules that combine to form maltose (draw What is a disaccharide? Draw the reaction of two glucose the structures) function of starch, cellulose, and glycogen. What are polysaccharides? Describe the structure and Study the diagrams below, which show carbohydrate molecules. Beside each molecule, write whether it is a monosaccharide, a disaccharide, or a polysaccharide. он CH OH H HOCH но он н нон Glucose он н CH2OH...
s he structure of sucrose ( 7) (4 pol (table Sugar) lactulose is shown below. Decide for each of the statements Label the glucose and fructose rings below whether it is True or False. нон он This ring is This ring is H2OH (T or F) Sucrose contains two acetal linkaes and no hemiacetal linkage. A. B. (T or F) Sucrose is a reducing sugar. C. (Tor F) Sucrose does not undergo mutarotation. D. (T or F) The glycosidic linkage...
need help!
21. The following sugars condense to form an α(1-4) glyosidic bond. Using the Haworth templates below, neatly number the carbons and draw in the new glycosidic bond OH он но H OH H OH 22. When fructose cyclizes, it forms a hemiacetal. Complete the structure for the a-fructose anomer CH2OH HO OH он CH2OH D-fructose Chem 1050 Exam 2 review problems 23. What are the products when the following two molecules undergo a condensation? 24. What are the...
Carbohydrates 1. Label each of the monosaccharides shown below as a triose, tetrose, pentoso, or hexose. но CH OH HT -он - он Н - ОН но -н но -Н но -н нон сньон он но -н НОН CH OH нон нон нон снон CH OH сон сон H- OH H- -он OH cң, он н-с-он Сн,он снон 2. Label each of the monosaccharides shown above as a ketose or aldose. 3. Identify all of the chiral carbons in the...
4. For each sugar below, characterize the anomer if a monosaccharide or the glycosidic bond(s) if a di- or polysaccharide (e.g., B,B-2,3; if there is more than one glycosidic bond, draw an arrow from each label to its corresponding bond). CH,OH CH2OH CH OН но н H Н H Он Н OH н OH Он Н ОН O H Но он b. a. OH H OH CH-OH O H Но ОН Н CH2OH CH2 CH2OH он OCH CH3 Но н...
y/node/845/take/3 Question 3 Classify the glycosidic linkage #3 in the structure shown below. Your answer must be in the form: type-#,# For example, alpha-2,3 or beta-4,6 Cн-он O H Hi H он HO H # 4 O H OH [X] CH2 O H HA CH, он сн,он CH,OH # 3 OH OH O H H H # 2 H H OH OH OH Hi OH но H OH # 1 H OH [W) H. H OH OH Answer Enter your...
18.
Which of the following compound(s) would undergo mutarotation in
aqueous solution?
19. Draw the chair conformation of a-D-galactopyranose.
20. Which of the following compound(s) is a glycoside?
21. Provide the reagents neccesary to carry out the following
conversion.
22. Predict the product(s) for the following reaction.
23. D-glucose & D-galactose are ______epimers of each
other.
24. Predict the product(s) for the following reaction.
25. Which of the following compound(s) would produce D-glucose
and D-mannose when treated with HCN followed...
1a-h
Chapters 21 and 22: 14 1. Consider the structure shown on the right and answer the following (4 questions about it (fill in blanks or circle proper choice). a. Its molecular formula is C H O and so it fits the general formula for a carbohydrate, which is Ca b. Specifically, this structure is (a D/ an L) (aldo/keto) (pent/hex) (ase/ose). c. Will it be optically active?_ d. If the top carbon was converted to a CH,OH, would it...
Page Chemistry 107 Midterm II Review Problems Draw a Lewis structure for CaHN (think over the bonding preferences of each atom when you lay out the skeleton of this molecule!) 1. CC Determine the geometry at each "central atom" (a) Does this molecule have any polar bonds? Is the entire molecule polar? (b) What will be the dominant intermolecular force in a sample of this compound? (c) (c) If you had 100.0 g of this compound, how many moles would...
Chapters 21 and 22: 1. Consider the structure shown on the right and answer the following questions about it (ill in blanks or cirele proper choice) (4 a. Its molecular formula is G ,H( )0( , and so it fits the CHOH , general formula for a carbohydrate, which is b. Specifically, this structure is (a D/ an L) (aldo/keto) (pent/hex) (aselose) c. Will it be optically active? d. If the top carbon was converted to a CH,OH, would it...
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