are all of these identical? 4. Determine if each of the following structures i) contain chiral centers. Label Chical...
4. Put an asterisk (*) next to each chiral center in the structure of erythronolide B, a metabone precursor to the commercial antibiotic, erythromycin. H3C .CH OH CH3 нс, Toi Erythronolide R Нас Анас OH 5. Determine whether the chirality centers in the following molecules have Rors configuration. (a) H (b) OCH2CH3 (c) OH NO-C-OH HC-CH3 H₃C-C-CH₂OH (a) HOH (b) c) HOCHZ HOCH2 CO2H 6. Are the following molecules chiral or achiral? If they are chiral, put an asterisk next...
2. For each of the pairs of compounds, indicate if they are identical, enantiomers, diastereomers, constitutional isomers or different compounds. Z-bromopropaneitrite Br CN constitutional isomers H2CH... CN CH3 CH3 COH Hanc HC HEN HS o n diastereomers MMCH₂CH₃ CH3 3. Identify the chiral centers in the diastereomers below and label each as Ror S. CHE
I 17 points shown below is the lipid lowering drue simvastatin, which contains soven chical centers stereogeni centers incle all the stereocenter Points will be deducted for incorrecta mente HO ICH HC Simvastatin (Lipid-lowering agent) 2.14 points) Give the complete IUPAC names, including Ror Sconfiguration for the following molecules IUPAC name (include Ror S) IUPAC name (include Ror S) 3. (4 points) Using dashed wedge representations, give the structures of the following molecules (5)-2-Bromopentane (R)-2-Pentanol Questions 4 & 5 relate...
4 Identily all the chiral centers with an asterisk () in each molecule and determine the absolute configuration as R or 5. See McMurry, sec. 5-5 and chap S PPT slides 16-22. NH h) Br
4. (26 points) Identify each chiral carbon in the molecules below with an asterisk (*) and assign R or s absolute configuration to each chiral carbon. Then, state (in the box provided) whether the molecules are enantiomers, identical, diastereomers, or not related. Hint: if it looks like a Fischer projection then it is a Fischer projection. ...1111 O піон аnd and .Ley O Era o C CHO CH,OH C. H oH and OHCH IH Сн,он
Extra Credit Worksheet NMU ID 1) Label all the chiral molecules with a circle. Label all meso compounds with a square (3 ps) OH OH 2) Determine the relationship of the following pairs of compounds. Are they identical, enantiomers, diastereomers, constitutional isomers or non-Isomeric different compounds? (4 ps) H internetu papra H-CH-CH Br+H CHE (d) 3) Draw the structures for the following compounds: (3 ps) (R. Z)-4-Ethyl-2-methylhept-5-en-3-one (S)-2-methyl-N-propylpentanamide 4) Give the IUPAC name corresponding to the following structure (Label the...
5. Consider the molecules shown below. (4 points) Identify all chiral centers in each molecule. • Determine whether each molecule is chiral or achiral. . If the achiral molecules are meso, classify them as such. OH ОН ОН
5. Consider the molecules shown below. (4 points) Identify all chiral centers in each molecule. • Determine whether each molecule is chiral or achiral. • If the achiral molecules are meso, classify them as such. он OH ОН
5. Consider the molecules shown below. (4 points) Identify all chiral centers in each molecule. Determine whether each molecule is chiral or achiral. If the achiral molecules are meso, classify them as such. ОН ОН он Cl Alacan.
3. For each of the following chiral molecules, indicate whether the enantiomer shown is the Ror Senantiomer. CH3 CH2-CHE чон NH, OH CH=CH2 4. A liquid mixture is comprised of a 50:50 mixture of the following two compounds. Which of the following statements is true? (Choose one) CH3 A) The liquid is a racemate. B) The liquid is a mixture of two constitutional isomers. C) The liquid is a mixture of two unrelated compounds. D) The compounds are identical; it...