Be sure to answer all parts. Complete the Fisher projection on the right, by labeling the...
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
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...
Convert the Fischer projection to the Haworth projection of the B-pyranose form by moving the substituents to the appropriate positions. The anomeric carbon is shown. EK Cyclization } CH2OH Answer Bank CH,OH OH H
Question 2 (1 point) The Fisher projection below is equivalent to which Haworth structure if the anomer formed is beta? CHO HO— 1 th 우 HI CH2OH CH OH OHA OH Он O2) CH2OH —о о ОН 3) CH,OH - О ОН ОН O4) CH OH ОН ОН ОН ОН
please help!! switching to all online is so hard 50. When the following Fischer projection closes, which is the alpha Haworth form? CH2OH EO A 7 Но он se a cozycy A) a CH2OH a on B) HONE LOH HO CH₂ OH HO C2 C3°" cho CH2OH Lornoon E) Two of these are correct 51. What is the correct relationship between the 2 compounds? CH₂OH сом C=O 40 - OH HOH CH₂OH A) diastereomers B) epimers C) enantionmers and H0+...
Complete the Haworth projection of -D-galactose by placing labels on the pyranose ring. Labels may be used more than once. Note, there are two different hydroxy labels-make sure the oxygen is next to the bond. Answer Bank HO OH H СН2ОН
Be sure to answer all parts. Complete the stepwise mechanism for the following reaction by ordering the choices below. H2SO4 & HO ОН + H20 HÖH Co-H HO: :ÖH H-OsOH HÖSOH HSO4 HO :O-H O: + HSO4 H2O + ta А B HO: OH HO::OH 20: II -ö-H HÖSOSH HO tutorstas 0: -OSO3H + HSO4 E F Step [1]: B Step [2]: A Step [3]: C Step [4]: E Step [5]: D Step [6]: F
3) Draw the disaccharide that is formed when the following two mon joined by a B (1-3) glycosidic linkage. (2 pts) two monosaccharides are CH₂OH онон - он снон, 9 w OH 3 OH CH, OH OH OH OR 0 Y 4) Consider the disaccharide sophorose, a product of the caramelization of glucose, answer the following questions: CH,OH Мон OH ОН a) Classify the glycosidic linkage as a or B, and use the numbers to designate its location. (1 pt)...
answer all Question 1. Redraw the following Newman projection as a Fisher project. Part of the Fisher projection is drawn as follow: 5-60-5 CIH Question 2. Answer the follow questions based on the energy diagram as shown below: Free Energy (G) Reaction Coordinate a. Identify the reactants and products on the following energy diagram Reactant product b. Identify B and C, and determine whether the reaction is endergonic or exergonic as drawn. c. Identify the position of transition state on...
3 attempts left Check my work Be sure to answer all parts. Draw the organic products formed when the monosaccharide is treated with each of the following reagents: [1] H2, Pd; [2] Cu2+, OH. CHO H2 HO с -H C+2 < Pd H с OH OH draw structure ... CH2OH draw structure ... Ask your instructor question