Which of the following characteristics is common among chiral pool substrates? Question 4Select one: A. They have good leaving groups B. They are all achiral C. All have a multiplicity of chiral centres D. They have poor leaving groups
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Which of the following characteristics is common among chiral pool substrates?
Question 4Select one:
A.
They have good leaving groups
B.
They are all achiral
C.
All have a multiplicity of chiral centres
D.
They have poor leaving groups
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- What is the relationship between the molecules shown? HO. HO same molecules constitutional isomers diastereomers O enantiomers ......1. L-aspartic acid + phosgene (COCl2)= ? 2.Draw the (S)-enantiomer of two sweeteners intermediate 4 + intermediate 5 = two sweeteners intermediate 6. (Intermediate 4 is the image provided)+ (Intermediate 5 is the product of number 1)= Intermediate 62. Mark any chirality centers (asymmetric carbons) with a *. How many stereoisomers are possible? Br
- III. Consider the compound below. H. F HO- HO -HO- (Atomic number: H-1, C-6, O-8, F-9) a. How many chiral centers are in the molecule? b. How many stereoisomers are there for the compound? c. Draw the Fischer projection for each of the stereoisomer and determine the absolute configuration (R or S). Label each using I, II, etc. d. Which pairs are enantiomers? Which are diastereomers?arch Click Submit to complete this assessment. Question 13 What is the relationship between these two compounds ? x a. same compounds Ob. constitutional isomers c. Enantiomers d. Diastereomers Et P hpWhich of the following describes an atactic stereoisomer? Select one: a. All of the R groups are situated on the same side of the chain b. All of the R groups alternate sides of the chain c. The R groups are randomly positioned on sides of the chain O d. All of the R groups are in the trans structure
- QUESTION 7 Assign R or S configuration to each indicated chirality center (carbon A and B) in the following molecule (Erythronolide B). Which of the following assignments is correct? CH, . CH, B HO, "OH OH CH3 Erythronolide B A a. carbon A (R); carbon B (S) b. carbon A (R); carbon B (R) c. carbon A (S): carbon B (R) d. carbon A (S): carbon B (S)3. For each of the following molecules, label each stereogenic center as R or S. Label the molecules appropriately as chiral or meso. a. d. e. H₂N₂ NHMe 850 ketamine •NH₂ m OH HS OH NH₂ cysteine (amino acid)Moving to another question will save this response. uestion 5 Refer to the structure of (S)-(-)-Serine below and choose the correct answer from option (A - ) COH (SH-)-Serine H HOH,C NH O A. is dextrorotatory. B. rotates plane-polarized light in a clockwise direction. OC. is racemic. D.rotates plane-polarized light in a counterclockwise direction. E. is optically inactive A Moving to another question will save this response. O Type here to search
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