The answer is A.
We use the CIP Rules to identify that the -OH group has the highest priority, followed by the -COOH group, -CH2OH group and finally the -H group. Now, since the -H (the group with the lowest preference) is not present at the lower vertical bond, we swap -H and -CH2OH. Since we must swap in pairs to ensure that the resulting compound is equivalent to the original, we swap the -OH and the -COOH groups as well. We can now check the direction in which the preference order 1 - 2 - 3 - 4 occurs. This gives us the R configuration (clockwise).
The configuration of R-(+)-glyceraldehyde is as follows: o II C-H H-I-OH CH2OH What is the configuration...
Drawings Instructor's approval of models L-glyceraldehyde Fischer: L-glyceraldehyde Fischer: D-glyceraldehyde H C Hico OH-c-H D-glyceraldehyde H-6-oh CH2OH CH2OH Fischer: L-glucose Fischer: D-glucose D-glucose Haworth: C-D-glucose Haworth: -D-glucose CE-D-glucose
Part I (15pts). Carbohydrates CH2OH H-C-OH H-C OH HO-C-H HO H-C-OH H-C-OH CH2OH H-C-OH H-C-OH CH2OH CH2OH Simple sugars have a molecular formula of Cn(120)n, what is the molecular formula for each sugar above. What is the name of each compound above-write it under the compound. Circle each chiral carbon in the molecules above. In what ways are the structures of D-glucose and D-galactose the same?
What is the chemical formula for this molecule? 6 CH2OH 5C, H H-C- 14 - O - I O-0-I H H 연애 HO OH IC 2] OH
Q1. Give R and S configuration to the following compounds (5 Marks) C2H5 i) H3C-C-H OH C2H5 ii) H2N-C-CH2-CH2-CH3 H ОН iii) H CH2-CH2-CI iv) HO-H2C-H2C-C-CH2-CH2-CH3 1 Н. C/ H2C H-C-CH3 CH2
QUESTION 9 In the Fischer projection of Glyceraldehyde shown below, CHO - H-C-OH - CH2OH The molecule is in the D-form The molecule in the L-form The-CHO group is facing forward The H group is facing backward, QUESTION 10 In O-linked and N-linked transmembrane glycoproteins, The side chains of amino acids present on the outside of the membrane are glycosylated The back-bone-NH and Co groups of amino acids present on the inside of the membrane are glycosylated. The side chains...
CH2OH O OH HO -H H OH CH2OH D-sorbose Name the two alditols formed when the above sugar undergoes reduction by NaBH4- Alditol 1: Alditol 2: Submit Answer Try Another Version 10 item attempts remaining
What metabolic pathway forms the following conversion OH I-O C=0 C=0 H-C-OH C=0 HO-C-H 2 4 H-CH H-C-OH H-C-OH H 1 CH2OH (A) Glycolysis (B) Kreb's Cycle (C) Chemiosmosis (D) Fermentation a.(a) Ob.(b) OC(C) d.(d) Moving to another question will save this response
designate R/S configuration
R-configuration configuration 15. ö lö H, OH CHE 18. 17. HECO HO Rco Nh-c Answer key correct but Error in movie for 16. s -cousuvachu H OH H CHI нон HEN2 19. I NH, NH2 Br., CHE 21. H 20, он Answer key correct but Error in movie for 20. нох | H NHÔ нсн. н. сня Η HO...IH 23. H₃C NH₂ H, CH, HO, CHE H, CH3 H., CHE нсна АН 26. HO CHE Hнсн,он HOYO...
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The missing product from the following reaction is OH NaOH + H20 COH Co Na* H A OrNa* A B C D Question 28 What is the name of the following ether compound? • Previous Which carbon is the alpha, a, carbon? I HO III II IV 11 III IV EXC o Na OH O" Na O Na OH Na Is this monosaccharide a Dor L sugar? CH2OH C=0 H ОН H ОН...
Question 7 Predict the major organic product of the reaction sequence, i. NH3, H20 M ii. dilute Ha, cold O O OH NH2 NH2 HO HO HN I II III H N HN IV V CA. V B. III C. 11 DIV E. I Question 8 Which of the following would be the strongest acid? NO2 COH COH COH ON ON "NO2 I II III COH COH NO2 ON "NO2 IV V A. IV B. III C. I D. II...