Homework Answers
For each compound given 1st is the monosaccharide on the left side
of the structure, 2nd is in the right side and then the anomeric
center and reducing or not.
6. D-Glucose on left, D-ribose on right the anomeric center is beta.The sugar is reducing as cyclic hemiacetal bond is there on one monosaccharide (right side).
7. D-Glucose on top, D-galactose on bottom the anomeric center is beta. The sugar is reducing as cyclic hemiacetal bond is there on one monosaccharide (upper one).
8. D-Glucose in left D-deoxyribose on right the anomeric center is alpha.The sugar is reducing as cyclic hemiacetal bond is there on one monosaccharide (right side).
9. Find the attached image file
10. Find the attached image file
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identify the monossacharides in the compound, the orientation at
the anomeric center(s) (alpha or beta), and...
Identify the monosaccharides in the compound, the orientation at the anomeric center(s) (a or B), and...
Identify the monosaccharides in the compound, the orientation at the anomeric center(s) (a or B), and the linkage sites between the sugars. Also indicate if it is a reducing sugar or not. CH, OH -0 OH но CH OH Isomaltulose CHEM 120 Essentials of Organic Chemistry Fall 2019 Gentiobiose 3. 언어 Isomaltose (Raffinose is responsible for the flatulence you get after eating beans.) (Name this trisaccharide from the top down.) To Raffinose OH MOOTH 6104 CHOH (Name this trisaccharide from...
7. For the following monosaccharides, give the corresponding Fischer projection. CH OH —0 ОН CH,он Но...
7. For the following monosaccharides, give the corresponding Fischer projection. CH OH —0 ОН CH,он Но —0 ОН НО У (он но У HO сно F 8. For the following monosaccharides, give one possible Haworth structure. CHO H- OH HOH Нонн — он нон CH OH CH OH от т т н-
anyone know how to do this? please help if so:) 29. Statements: (1) Cellulose and amylose...
anyone know how to do this? please help if so:)
29. Statements: (1) Cellulose and amylose are glucose polymers which differ in the type of glycosidic linkage present (2) All monosaccharides are either aldoses and ketoses. (3) Enantiomers can never be epimers. a) all three statements are true b) two of the three statements are true c) only one of the statements is true d) none of the statements is true For each of the stereochemical descriptions select from the...
Question 2 Identify all D-monosaccharides below: CHO НЕОН НОН Н -ОН НОНЕН CHO НО. -Н НОН...
Question 2 Identify all D-monosaccharides below: CHO НЕОН НОН Н -ОН НОНЕН CHO НО. -Н НОН НО-НН НО. -Н НО -Н CH2OH ІІ H Н ОН 0= НО-Н НЕОН Н ОН CH2OH CHO Н- -ОН НОН НЕОН НО-Н НЕОН CH OH IV — о Н- НОНЕН Н- ОН НО-Н Н ОН НО НО- CH2OH Ео Н ОН -Н -Н Н. -ОН Н VI CH2OH H ОН 0 Н- НО. -Н НО -Н Н VII Н Нон 0= НЕОН НО-НН НО....
2. Please refer to the monosaccharides shown below to the following questione (i) CHOA City CH....
2. Please refer to the monosaccharides shown below to the following questione (i) CHOA City CH. OH CAO CH2014 SHO LO HOH o A- HOH Анон HAH Hotu Нон H OM 40+ CHOA HOH 4-104 HOH HO нон c, or (404 CH₂OH A. Sorbose B. Rhamnose C Erythrulose D. Xylulose E. Glucose ) Classify each sugar by type: ketoheptose, aldo butase etc. Sorbose Rhamnose Erythrulose Xylulose Glucose from the sugars above, choose the one(s) that fit each description below ii)...
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...
5.59 Provide the products and balance the following reac tion for the complete combustion of pentane,...
5.59 Provide the products and balance the following reac tion for the complete combustion of pentane, C;H12 Identify the reactant that is oxidized and the reactant 5.65 that is reduced. CsH12) 02() 5.60 Provide the products and balance the following reac- tion for the complete combustion of the fatty acid octanoic acid, C H1602. Identify the reactant that is oxidized and the reactant that is reduced. CgH1602(s) O2 (g) 5.62 Identify the reactant that is oxidized and the reactant that...
draw fisher projections for both the D and L isomers of the following 12 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CHO b. a. CH,OH C=O...
draw fisher projections for both the D and L isomers of the
following
12 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CHO b. a. CH,OH C=O он HOH HOH но CH,OH CH,OH 3 Draw Fischer projections for both the D and L isomers of the following a. 2,3-dihydroxypropanoic acid b. 2-chloro-3-hydroxypropanoic acid Draw Fischer projections for both the D and L somers of the following amino acids:...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH OH OH c. 3 d. 4 Que. 10) What is the relationship between D-erythrose and D-threose? CHO CHO HOH HOH H OH OH CHOH CH,OH D-Erythrose D-Threose a. constitutional isomers b. enantiomers c. diastereomers d. tautomers Que. 11) What is the relationship between D-ribose and D-xylose? CHO CHO І н он н -он нон нон н -он н -он І І CH OH Сн,он...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D)...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D) below based on carbonyl group and number of carbons (c.8. aldohexose, ketotriose, etc.). Classify them as an antiomer. Indicate the number of chiral carbons for each sugar. Sugar Classification based on carbonyl group and number of carbons Lor D enantiomer Number of chiral carbons н-с-он HO-6-H. н-с-он ін,он CH,OH C=0 HO-C-H н-с-он HO-C-H. ён,он снон c=0 | HO-C-H ін,он H-C-OH CH, OH CD 2....
Identify the monosaccharides in the compound, the orientation at the anomeric center(s) (a or B), and the linkage sites between the sugars. Also indicate if it is a reducing sugar or not. CH, OH -0 OH но CH OH Isomaltulose CHEM 120 Essentials of Organic Chemistry Fall 2019 Gentiobiose 3. 언어 Isomaltose (Raffinose is responsible for the flatulence you get after eating beans.) (Name this trisaccharide from the top down.) To Raffinose OH MOOTH 6104 CHOH (Name this trisaccharide from...
7. For the following monosaccharides, give the corresponding Fischer projection. CH OH —0 ОН CH,он Но —0 ОН НО У (он но У HO сно F 8. For the following monosaccharides, give one possible Haworth structure. CHO H- OH HOH Нонн — он нон CH OH CH OH от т т н-
anyone know how to do this? please help if so:)
29. Statements: (1) Cellulose and amylose are glucose polymers which differ in the type of glycosidic linkage present (2) All monosaccharides are either aldoses and ketoses. (3) Enantiomers can never be epimers. a) all three statements are true b) two of the three statements are true c) only one of the statements is true d) none of the statements is true For each of the stereochemical descriptions select from the...
Question 2 Identify all D-monosaccharides below: CHO НЕОН НОН Н -ОН НОНЕН CHO НО. -Н НОН НО-НН НО. -Н НО -Н CH2OH ІІ H Н ОН 0= НО-Н НЕОН Н ОН CH2OH CHO Н- -ОН НОН НЕОН НО-Н НЕОН CH OH IV — о Н- НОНЕН Н- ОН НО-Н Н ОН НО НО- CH2OH Ео Н ОН -Н -Н Н. -ОН Н VI CH2OH H ОН 0 Н- НО. -Н НО -Н Н VII Н Нон 0= НЕОН НО-НН НО....
2. Please refer to the monosaccharides shown below to the following questione (i) CHOA City CH. OH CAO CH2014 SHO LO HOH o A- HOH Анон HAH Hotu Нон H OM 40+ CHOA HOH 4-104 HOH HO нон c, or (404 CH₂OH A. Sorbose B. Rhamnose C Erythrulose D. Xylulose E. Glucose ) Classify each sugar by type: ketoheptose, aldo butase etc. Sorbose Rhamnose Erythrulose Xylulose Glucose from the sugars above, choose the one(s) that fit each description below ii)...
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...
5.59 Provide the products and balance the following reac tion for the complete combustion of pentane, C;H12 Identify the reactant that is oxidized and the reactant 5.65 that is reduced. CsH12) 02() 5.60 Provide the products and balance the following reac- tion for the complete combustion of the fatty acid octanoic acid, C H1602. Identify the reactant that is oxidized and the reactant that is reduced. CgH1602(s) O2 (g) 5.62 Identify the reactant that is oxidized and the reactant that...
draw fisher projections for both the D and L isomers of the
following
12 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CHO b. a. CH,OH C=O он HOH HOH но CH,OH CH,OH 3 Draw Fischer projections for both the D and L isomers of the following a. 2,3-dihydroxypropanoic acid b. 2-chloro-3-hydroxypropanoic acid Draw Fischer projections for both the D and L somers of the following amino acids:...
Que. 9) What is the major organic product obtained from the following reaction? H2SO4 o OH OH OH c. 3 d. 4 Que. 10) What is the relationship between D-erythrose and D-threose? CHO CHO HOH HOH H OH OH CHOH CH,OH D-Erythrose D-Threose a. constitutional isomers b. enantiomers c. diastereomers d. tautomers Que. 11) What is the relationship between D-ribose and D-xylose? CHO CHO І н он н -он нон нон н -он н -он І І CH OH Сн,он...
Culhydrates 1. Complete th Complete the table by classifying each sugar sugar (A, B, C, D) below based on carbonyl group and number of carbons (c.8. aldohexose, ketotriose, etc.). Classify them as an antiomer. Indicate the number of chiral carbons for each sugar. Sugar Classification based on carbonyl group and number of carbons Lor D enantiomer Number of chiral carbons н-с-он HO-6-H. н-с-он ін,он CH,OH C=0 HO-C-H н-с-он HO-C-H. ён,он снон c=0 | HO-C-H ін,он H-C-OH CH, OH CD 2....
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