12.100 Convert each three-dimensional representation into a Fischer CH3 CHO projection OCH2CH3 a. CH3-CH b. HO-C-CH3...
Convert the Fischer representation shown below into a line-angle drawing with the proper stereochemistry. CHO HO H H ОН Br -H CH,COOH
12. Which Fischer projection corresponds with the following molecule? CHO CHO H- OH CHO Ho- Br HD--- H -- Et CH.CH CH₂ CH2 Brott CH₂ CH₃ al diIV e.v c III
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
10. Convert the following 3-dimensional molecule into a Fischer projection looking along the indicated line of sight. Assign an R or S designation for the absolute configuration to the chiral C. Is the molecule at the right the same or the enantiomer of the original molecule? NH2 NH2 HO CH3 OH HC H
A Fischer projection of a monosaccharide is shown below: CHO H- ОН HO -H CH2OH to forma ring. Note that the numbering of When this monosaccharide cyclizes, carbon bonds to the oxygen on carbon the carbons begins at the top of the Fischer projection. Submit Answer Retry Entire Group 6 more group attempts remaining [Review Toples [References A Fischer projection of a monosaccharide is shown below: CH2OH C=0 H- OH HO H CH2OH to form a ring. Note that the...
Convert the Fischer representation shown below into a line-angle drawing with proper stereochemistry. [File Response] CHO HO H H OH Br -Н CH2COOH ait oly not alonla alvejad erial woled benutului de
6.5 poin Convert the Fischer representation shown below into a Ine-angle drawing with the proper stereochemistry. CHO HO H H H CH,COOH Attach File Browse My Computer Browse Content Collection Browse Dropbox
12.36 Draw Fischer projections for each of the following dash-wedge structures: a. CHO b. CHO C. CHO с но : Br CH OH Ho : н СН,ОН н : ОН СН,ОН
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
9) Idose can be both oxidized and reduced. Draw the Fischer projection of both products CHO HO HO -H CH OH Reduction Product D-isomer Oxidation Product L-isomer 12) If you have type AB blood, which of the following statements would be true? -a. You would have type A antigens -b. You would have type A and type B antibodies c. You would have no antibodies d. You would have type A and type B antigens