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For the monosaccharide shown on the right, answer the
following questions: A-E please
1. For the...
Disaccharides are joined by glycosidic bonds formed between the anomeric carbon on one monosaccharide and a...
Disaccharides are joined by glycosidic bonds formed between the
anomeric carbon on one monosaccharide and a hydroxyl (–OH) group of
another monosaccharide. Identify the types of linkages in each of
the following three disaccharides.
Identify the types of linkage.
100 12 13 14 15 16 17 95 Question 14 of EA Sapling Learning Disaccharides are joined by glycosidic bonds formed between the anomeric carbon on one monosaccharide and a hydroxyl (-OH) group of another monosaccharide. Identify the types of linkages...
PRELABORATORY EXERCISE 11 1 Provide a term that matches each description below. a Monosaccharides that contain...
PRELABORATORY EXERCISE 11 1 Provide a term that matches each description below. a Monosaccharides that contain a ketone functional group b Carbohydrate composed of many monosaccharide subunits c Reaction that involves the breaking of large molecules into smaller units d Generic term for a carbohydrate that can be oxidized with Cu?" e Carbohydrate composed of two monosaccharides linked through a glycosidic bond f Monosaccharides that contain an aldehyde functional group 2 Circle the anomeric carbon in each monosaccharide component of...
1) a. Please draw the structure of the intermediate in the process shown below. CH2OH CH2OH...
1) a. Please draw the structure of the intermediate in the process shown below. CH2OH CH2OH Кон о он КОН OH OH OH OH OH The process shown above is called: c. Please mark an anomeric carbon and designate the orientation of the hydroxyl group. d. Indicate the carbon that determines the D or L configuration in the glucopyranose above by number or with an X. e. Is this a reducing sugar? f. Can it react with another carbohydrate to...
1- Sucrose does not react with Fehling's reagent because A- Sucrose is not a reducing sugar....
1- Sucrose does not react with Fehling's reagent because A- Sucrose is not a reducing sugar. B) The anomeric carbon of glucose is involved in the glucose- fructose bond and hence is not free to form the aldehyde in solution. C) The monosaacharide constituents of sucrose no longer have an anomeric carbon with a free potential aldehyde or ketone group, and therefore no longer exhibits reducing properties. D) sucrose is a disaccharide of glucose and fructose in which the oxygen...
22. Which of the following features NOT red by W ares A Moscowrides betydrolyzed wpter carbohydrates...
22. Which of the following features NOT red by W ares A Moscowrides betydrolyzed wpter carbohydrates 11) Mochides will C Moncuccharides tuve i detyder skete D) Mononcerides centove or more alcohol group 26. Which of the following tyres of hohydrates can be hydrolyzed to give smaller molecules? 1. Monosaccharides 1 Disaccharides TIT. Oligosaccharides IV. Polysaccharides A) I only B) II and IV only C) III only D) I and II only E) II. HII and IV C) 4 27. The...
Question 5 (of 31 00 points Select the keyword or phrase that will best complete each...
Question 5 (of 31 00 points Select the keyword or phrase that will best complete each sentence. Key terms: is a carbohydrate that has the OH group on the chirality L a anomer center farthest from the carbonyl on the right. -glycoside A(n) is the cyclic form of a D-monosaccharide that contains a hemiacetal with the OH group drawn up, above the ring Banomer B-glycoside D-monosaccharide Ain) is a monosaccharide with the OR group on the anomeric carbon oriented below...
Sucralose, Part 2 5 of 7 Which group should you draw an arrow from and which group should you dra...
Sucralose, Part 2 5 of 7 Which group should you draw an arrow from and which group should you draw that arrow to on the Fischer projection shown below to indicate the nucleophilio attack that must occur to cyclize this monosaccharide to form the monomer structure shown on the right in the dissacharide A CH2CI 2 но-c он 3 он 4 CH2Cl Reset Help carbon D Arrow from to Part B Which of the following describes the ring on the...
PRELABORATORY EXERCISE 1 Provide a term that matches each description below. a Monosaccharides that contain a...
PRELABORATORY EXERCISE 1 Provide a term that matches each description below. a Monosaccharides that contain a ketone functional group b carbohydrate composed of many monosaccharide subunits c Reaction that involves the breaking of large molecules into smaller units d Generic term for a carbohydrate that can be oxidzed with cu e Carbohydrate composed of two monosaccharides inked through a gycosidic bond f Monosaccharides that contain an aldehyde functional group 2 circle the anomeric carbon in each monosaccharide component of the...
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....
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...
Disaccharides are joined by glycosidic bonds formed between the
anomeric carbon on one monosaccharide and a hydroxyl (–OH) group of
another monosaccharide. Identify the types of linkages in each of
the following three disaccharides.
Identify the types of linkage.
100 12 13 14 15 16 17 95 Question 14 of EA Sapling Learning Disaccharides are joined by glycosidic bonds formed between the anomeric carbon on one monosaccharide and a hydroxyl (-OH) group of another monosaccharide. Identify the types of linkages...
PRELABORATORY EXERCISE 11 1 Provide a term that matches each description below. a Monosaccharides that contain a ketone functional group b Carbohydrate composed of many monosaccharide subunits c Reaction that involves the breaking of large molecules into smaller units d Generic term for a carbohydrate that can be oxidized with Cu?" e Carbohydrate composed of two monosaccharides linked through a glycosidic bond f Monosaccharides that contain an aldehyde functional group 2 Circle the anomeric carbon in each monosaccharide component of...
1) a. Please draw the structure of the intermediate in the process shown below. CH2OH CH2OH Кон о он КОН OH OH OH OH OH The process shown above is called: c. Please mark an anomeric carbon and designate the orientation of the hydroxyl group. d. Indicate the carbon that determines the D or L configuration in the glucopyranose above by number or with an X. e. Is this a reducing sugar? f. Can it react with another carbohydrate to...
22. Which of the following features NOT red by W ares A Moscowrides betydrolyzed wpter carbohydrates 11) Mochides will C Moncuccharides tuve i detyder skete D) Mononcerides centove or more alcohol group 26. Which of the following tyres of hohydrates can be hydrolyzed to give smaller molecules? 1. Monosaccharides 1 Disaccharides TIT. Oligosaccharides IV. Polysaccharides A) I only B) II and IV only C) III only D) I and II only E) II. HII and IV C) 4 27. The...
Question 5 (of 31 00 points Select the keyword or phrase that will best complete each sentence. Key terms: is a carbohydrate that has the OH group on the chirality L a anomer center farthest from the carbonyl on the right. -glycoside A(n) is the cyclic form of a D-monosaccharide that contains a hemiacetal with the OH group drawn up, above the ring Banomer B-glycoside D-monosaccharide Ain) is a monosaccharide with the OR group on the anomeric carbon oriented below...
Sucralose, Part 2 5 of 7 Which group should you draw an arrow from and which group should you draw that arrow to on the Fischer projection shown below to indicate the nucleophilio attack that must occur to cyclize this monosaccharide to form the monomer structure shown on the right in the dissacharide A CH2CI 2 но-c он 3 он 4 CH2Cl Reset Help carbon D Arrow from to Part B Which of the following describes the ring on the...
PRELABORATORY EXERCISE 1 Provide a term that matches each description below. a Monosaccharides that contain a ketone functional group b carbohydrate composed of many monosaccharide subunits c Reaction that involves the breaking of large molecules into smaller units d Generic term for a carbohydrate that can be oxidzed with cu e Carbohydrate composed of two monosaccharides inked through a gycosidic bond f Monosaccharides that contain an aldehyde functional group 2 circle the anomeric carbon in each monosaccharide component of the...
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....
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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