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in the monosaccharide A show in problem 7, identify carbon
number 2 by drawing an arrow...
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...
1) SHOW WORK STEP By STEP below is Figure 7-3 Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-...
1) SHOW WORK STEP By STEP
below is Figure 7-3
Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-allose, (b) D-gulose, and (c) D-ribose at C-2, C-3, and C-4. Answer Epimers differ by the configuration about only one carbon. (a) D-altrose (C-2), D-glucose (C-3), D-gulose (C-4) (b) D-idose (C-2), D-galactose (C-3), D-allose (C-4) (c) D-arabinose (C-2), D-xylose (C-3) (a) D-Aldoses Three carbons Four carbons Five carbons но не HO -OH н-с-он CH, OH D-Glyceraldehyde но-с-н H-C-OH снион D-Threose...
Part D Glucose can be classified as an aldohexose. Name the following monosaccharide to indicate its...
Part D Glucose can be classified as an aldohexose. Name the following monosaccharide to indicate its carbonyl group and the number of carbon atoms. но он он н -C- C-C-C-C OH HHHH Spell out the name of the monosaccharide, including the carbonyl group and the number of carbon atoms. View Available Hint(s) (3R 4R)-1,3,4,5-tetrahydroxyponta Submit Previous Answers X Incorrect; Try Again; 3 attempts remaining Part B Indicate the chiral carbon(s). Identify the appropriate atom by selecting each atom and assigning...
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...
Carbohydrates homework 1. Identify the sugars as aldose or ketose, Lor D, and determine the number...
Carbohydrates homework 1. Identify the sugars as aldose or ketose, Lor D, and determine the number of Chiral centers. Сон CHO к он СКО КО- { ой -Н НО Н и о ко ги но И. н 애 CHROM ch, Сон и D Сн оя ь, о H он и к ой ho И 10. И и — ой ch 20h CH₂oh 2. Identify the relation between the structures in each of the following pairs. СКО СКО Си0 Cheon И...
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....
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons...
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons...
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...
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...
Problem 7. Let U1,U2,... be independent random variables all uniformly distributed on the unit interval, and let N be the first integer n 2 2 such that Un > Un-1. Show that for each real number 0&...
Problem 7. Let U1,U2,... be independent random variables all uniformly distributed on the unit interval, and let N be the first integer n 2 2 such that Un > Un-1. Show that for each real number 0<u < 1 !-un . 1- e-". (a) P(Ui-u and N = n) = (b) PUI S u and N is even)
Problem 7. Let U1,U2,... be independent random variables all uniformly distributed on the unit interval, and let N be the first integer...
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...
1) SHOW WORK STEP By STEP
below is Figure 7-3
Recognizing Epimers Using Figure 7-3, identify the epimers of (a) D-allose, (b) D-gulose, and (c) D-ribose at C-2, C-3, and C-4. Answer Epimers differ by the configuration about only one carbon. (a) D-altrose (C-2), D-glucose (C-3), D-gulose (C-4) (b) D-idose (C-2), D-galactose (C-3), D-allose (C-4) (c) D-arabinose (C-2), D-xylose (C-3) (a) D-Aldoses Three carbons Four carbons Five carbons но не HO -OH н-с-он CH, OH D-Glyceraldehyde но-с-н H-C-OH снион D-Threose...
Part D Glucose can be classified as an aldohexose. Name the following monosaccharide to indicate its carbonyl group and the number of carbon atoms. но он он н -C- C-C-C-C OH HHHH Spell out the name of the monosaccharide, including the carbonyl group and the number of carbon atoms. View Available Hint(s) (3R 4R)-1,3,4,5-tetrahydroxyponta Submit Previous Answers X Incorrect; Try Again; 3 attempts remaining Part B Indicate the chiral carbon(s). Identify the appropriate atom by selecting each atom and assigning...
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...
Carbohydrates homework 1. Identify the sugars as aldose or ketose, Lor D, and determine the number of Chiral centers. Сон CHO к он СКО КО- { ой -Н НО Н и о ко ги но И. н 애 CHROM ch, Сон и D Сн оя ь, о H он и к ой ho И 10. И и — ой ch 20h CH₂oh 2. Identify the relation between the structures in each of the following pairs. СКО СКО Си0 Cheon И...
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....
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...
ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...
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...
Problem 7. Let U1,U2,... be independent random variables all uniformly distributed on the unit interval, and let N be the first integer n 2 2 such that Un > Un-1. Show that for each real number 0<u < 1 !-un . 1- e-". (a) P(Ui-u and N = n) = (b) PUI S u and N is even)
Problem 7. Let U1,U2,... be independent random variables all uniformly distributed on the unit interval, and let N be the first integer...
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