the given compound we write in fischer projection based on absolute configuration R/S
we observe same configuration in wedg-dash and fischer projection
12. Which Fischer projection corresponds with the following molecule? CHO CHO H- OH CHO Ho- Br...
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
10. Which Fischer projection corresponds with the following molecule? Br CHO CHO CHO СНО CHO OHHO- HOH HOB HO- - Br H Br Br Br CH.CH CH2CHE CH2CH3 CH2CH) CH2CHE III IV TIT II d. IV e. V b.
Q: which structure beat represents the following disubstituted cuclohexane? Q: which fisher projection corresponds with the following molecule? 8. Whien structure best represents the foliowing disubstituted cyclohexane? Cн CHs H. нс нс CH CHs II d. I V a. b. III е. IV с. 9. Which of the following molecules has the highest melting point? но IV Ш I п d. II III a. e. b. IV I с. 10. Which Fischer projection corresponds with the following molecule? Br HO...
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...
8. Use the image to answer the questions that follow HO-CH HO-CH2 HO-CH2 CHO H₂o OH CHO CHO OCH CHOICH CH-OH CHCc CHOICH CH 10 | | CH-CH HỒ CH-CH CH-CH CH-CH CH-CH но он но HO он но OH OH HO A B C D Do not e How many carbons does each of the above sugars contain? Name to E n ipo Which sugars are aldoses and which are ketoses? Identify each sugar. Name the linkage for each...
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...
Draw fischer projection 1. (a) Draw the Fisher projection f H CH2SH OH Br CH2SH CH3 HSH2 CH3 Br CH SH OH
A Fischer projection of a monosaccharide is shown below: A Fischer projection of a monosaccharide is shown below: CHO H + -OH CH2OH Classify this monosaccharide (e.g., aldotriose) Does it have the D or L configuration? A Fischer projection of a monosaccharide is shown below: CH2OH Ç=0 H- -OH HO -H CH OH Classify this monosaccharide (e.g., aldotriose) Does it have the D or L configuration?
CH OH HO 100% Me CO-Et HB 2 H-O EtOH AcOH 68% Br T8 Me 77% CH 0H 2 10% HCI in MeCN 1) TsCllpy 2) Nal LDA H (cat.) Me Me 75% CH-OH CH2 Me (8 6 Draw wedge/dash drawing of the following Fischer projection scheme 1-8 and assign the stereocenter(s) R or S absolute configuration
consider this Fischer projection for a monosaccharide. the carbons are numbered for reference. which carbon is used to designate the enantiomer if the sugar Consider this Fischer projection for a monosaccharide. The carbons are numbered for reference. Which carbon is used to designate the enantiomer of the sugar? 1 CHO H HO 3 H H H -OH OH 4 -OH 5 CH,OHG