12.36 Draw Fischer projections for each of the following dash-wedge structures: a. CHO b. CHO C. CHO с но : Br...
Draw the Haworth projection structures for the B- anomer for these Fischer projections. raw Haworth projection structures for the B-anomer for these Fisch ojections CHO CHO ОН НО -Н H Н -ОН НО -Н Н -ОН CH2OH (D)-idose НО-НН НО-НН ньон снон (D)-galactose
draw fisher projections for both the D and L isomers of the following 12 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CHO b. a. CH,OH C=O он HOH HOH но CH,OH CH,OH 3 Draw Fischer projections for both the D and L isomers of the following a. 2,3-dihydroxypropanoic acid b. 2-chloro-3-hydroxypropanoic acid Draw Fischer projections for both the D and L somers of the following amino acids:...
2a. Draw the dash-wedge structures and Fischer projections of the following molecules. R-1-bromoethanol (2S, 3R) - 2-chloro-3-iodobutan-1-ol (HOCH-CHCICHBCH) .. Draw a diastereomer for (2S, 3R) - 2-chloro-3-iodobutan-1-ol.
Give the structures using both the dash-and-wedge (3D or perspective) formula and Fischer projections for each of the following compounds. a) (3S,4R)-3-bromo-4-methylhexane b) (2R,3R,4S,5S)-2,4-dibromo-5-chloro-3-methylhexane
7.11 Identify each of the following as a D or an L form and draw the structural formula of the enantiomer: CH,OH a. CHO b. c=0 НО -Н - HO —н но- ннон CH,OH СН,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
QUESTION 4 Which of the following Fischer projections corresponds to the compound shown below? НОН H,C, X Br CHz CH; CH3 сн; CH, НЕОН н—ОН НОЁН НОНН H-HBr Br-н H-Br BrEH Сн, сн, ён, CH, А) В) CH -
2. Draw Fischer projections of the open chain tautomer of each of the monosaccharides shown below, and indicate whether the compound is: i. an aldose or a ketose; ii. a D- or an L-sugar; iii. a triose, tetrose, pentose or hexose OH OH HO HO HO OH OH HO OH OH HO H OH 3. Draw Fischer projections of L-arabinose, D-fucose, and L-mannoheptulose given the structures below OH CHO CHO HOH HOH HOHH H-OH HOH H OH H OH OH...
Question 12 Which Fischer projection corresponds with the following molecule? Br OH CHO CHO CHO CHO CHO H ОН HO -H HO- Br HO -H -H H- -Br HE -Br Br -H Br -H CH2CH, CH,CH, CH2CH3 CH2CH3 снясно II III IV y ΟΙ O II O III O IV V
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....