10. Which Fischer projection corresponds with the following molecule? Br CHO CHO CHO СНО CHO OHHO-...
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
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...
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
14. Consider some of the 16 different stereoisomers of the following sugar: CHO ÇHO сно CHO CHO H OH HOHH OHHO+ HH OH H-OH нон HO+H HOTH Антон H OH нон H +OHH OHHO+H H-OH H+OH Антон нон нтон снуон CH OH CHO CHOH CHOH D-allose D-aitrose D-glucose D-mannose D-gulose - 140 +33° +53 +14° -20° CHO HO+ HO+H HO+H HO- H CHOH L-allose CHO CHO сно CHO H+H HOH OH OH HO- H нон нон нонн HO+H Нонн нонн...
Question 32 Which structure is an enantiomer of structure B? CHO сно CHO CHO CHO CHO нь HO -он HOH H -он но- он H. HOH он H- Нанон HOCH Hнон HOH н-ном но Hн HOH Нон нон сон сон сон сон E F ОН HE D Снон B с сон А Structure E Structure A Structure D Structure C Structure Question 33
I need some help to answer these following questions. Thanks. 41. Which molecule(s) is/are aromatic? I1 IV (A) I only (C) I, III, and IV (B) I and IV (D) I, II, III, and IV OH OH 42. Which Fischer projection represents this structure? HO OH OH H CHO CHO (A) H-OH (B) HOH HOH CH2OH CH2OH CHO HOH CHO но -н CH2OH CH2OH 43. Which is a product of this ozonolysis reaction? 1.03 2. (CH3)2S H O I BHs/THF...
24. Which of the structures are of the D configuration? 1 CHO I. CHO | III. CHO IV. HO H-C-OH H-C-OH HOC_H НО-С-н H–C-OH HO_C_H H-C-OH HOC_H CH CH CH CH,OH a. b. c. d. e. I and IV I and III I and II II and III II and IV 25. A compound, CH, NO, is hydrolyzed by strong acid, followed by neutralization to give C,H,O, and C,H.N. The CHN compound reacts with HNO, to give nitrogen gas. The...
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-
1. Which of the following types of isomer differs only by the rotation about single bonds? a. d diastereomers constitutional b. configurational e enantiomers c conformational 2. The Newman projection looking down the indicated bond in the following species is best represented by which of the following (, I, I, IV, or V)? Br HC H. н. CI сн, Br нс HC Br IV I1 а. I b II e.v c. III 3. Which substituents are anti to each other?...
Indicate which Haworth projection corresponds to the beta-pyranose form of the Fischer projection below. Compound A Compound B Compound C Compound D Compound E Compound A Compound B Compound C Compound D Compound E