please help!! switching to all online is so hard 50. When the following Fischer projection closes,...
Convert the Fischer projection to the Haworth projection of the B-furanose form by moving the substituents to the appropriate positions. The anomeric carbon is shown. Convert the Fischer projection to the Haworth projection of the B-furanose form by moving the substituents to the appropriate positions. The anomeric carbon is shown. CH2OH =0 HO—C—H Cyclization H-¢-OH Answer Bank CH OH H—¢-OH CH,OH CH2OH
A Fischer projection of a monosaccharide is shown below: A Fischer projection of a monosaccharide is shown below: CHO H- -ОН HO -H HO -H I -OH CH2OH v to form ring. When this monosaccharide cyclizes, carbon v bonds to the oxygen on carbon Note that the numbering of the carbons begins at the top of the Fischer projection. furanose pyranose A Fischer projection of a monosaccharide is shown below: CH2OH C=0 H OH НО. -H CH OH v to...
Select all of the descriptions that are accurate for this molecule of glucose CH2OH н с— о, н VH С он н C OH но с H Он it is a hexose it is in the alpha form it is in the beta form it is a furanse it is a pyranose it is a Haworth projection It is a Fischer projection Select all of the descriptions that are accurate for this molecule. CH-он Он Он ОН It is a...
ÇI-lagl- (2 pts) Use the Fischer projection shown below for the sugar D-altrose to draw a Haworth projection of the beta- 2. pyranose form of this sugar. но -Н H- OH H- OH OH H- CH-ОН 1
1a. For this question, select the LETTER of the structure that corresponds to the given Fischer projection. Select "NONE" if none of the structures are correct. но -н но-Ен нон он сн он CH2OH ни он СН2ОН Они — он он на он ин н но Он на и он н нон нон 1- — о сн,он СН2ОН но он Онон ХОН н на но Он ни ин нон 1b. For this question, select the LETTER of the structure that...
22. Convert the following Fisher projection into a Haworth projection. Draw only the alpha anomer (12 points) 21. Are the following pairs of carbohydrates the same, completely different, constitutional isomers or stereoisomers? (12 points at 3 points each) CHO CHO CHO сњон он OH он он CH2OH он он он он он но он но но он он CH2OH CH2OH он CHO CHO CHO сњон он он он он он но он но но Ho но он но он OH...
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-
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН НО- ОН НО ОН о H н ОН HO н НО Н НО H OH О Н H ОН но H НО H Н ОН OH о H Н ОН
Question 57 Choose the Fischer projection for the open-chain form of the following cyclic monosaccharide. ОН НО- ОН НО ОН о H н ОН HO н НО Н НО H OH О Н H ОН но H НО H Н ОН OH о H Н ОН
rever; mbine - you 13.78 Identify the Fischer projection A to D that matches each of the following: (13.1, 13.3) a. the L enantiomer of mannose b. a ketopentose c. an aldopentose d. a ketohexose о но СН,ОН НЕОН CHOH С=0 НЕОН H- С=0 НЕ ОН НО -н НО-н Но Hн НО -Н НЕОН НО - H н -ОН НОН CHOH СН,ОН СН,ОН CH,OH -ОН dic D