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What is the best way to physically separate enantiomers in the lab?
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- Use the figure below to answer the following questions. CI Cl CI Molecule 1 Molecule 2 Molecule 3 Molecule 4 Molecule 5 a. Which molecule(s) is/are enantiomers of Molecule 1? b. Which molecules(s) is/are diastereomers of Molecule 1? c. Which molecule is identical to Molecule 1? d. How many different stereoisomers are there for 1-chloro- 3-methylcyclopentanel? e. Which of the following molecules DO NOT rotate light?Consider a solution made up of 90% R and 10% S. What is the enantiomeric excess (ee%) of the R enantiomer?Please help with row 3 highlighted in yellow (column 1 and column 2); the instructions for the specific column in row 3 are above row 1: Follow the instructions in each column. Hint for the last column: draw it with a wedge and again with adash – which gives the correct configuration?
- Draw the mirror image enantiomers of 3-methylhexane1a. How many stereogenic centers are present 1c. Draw a three-dimensional structure of a in the structure below? Indicate them with asterisk(s). How many stereoisomers stereoisomers are possible? chiral compound with the molecular formula of C4H4Cl₂ that does not have a stereogenic carbon. In addition, draw the enantiomer of this compound. Number of stereogenic centers: Number of stereoisomers possible: 1b. Draw one of the two most stable stereoisomers of the compound in 1a using a planar structure with wedges and dashes. Now draw it in its preferred chair conformation. 1d. Draw two meso compounds with the molecular formula of C7H14.Using Enantiomeric Excess to Calculate the Amount of Each Enantiomer If the enantiomeric excess is 95%, how much of each enantiomer is present?
- Please just explain why these are the correct answers, thanks!What is the percent enantiomeric excess (ee) of a mixture that has 86% of one enantiomer and 14% of the other? 100% 43% 4% O 14% O 72% 614%Identify the type of configurational isomerism that exist for each double bond or chiral carbon in the structure. Use E-Z system for A and R and S system for B.
- Please ASAPExplain the difference between an enantiomer and an epimer. a. Enantiomers are non-superimposable mirror image structures. Epimers are diastereomers that differ only in the orientation of one chiral center. b. Epimers are non-superimposable mirror image structures. Enantiomers are diastereomers that differ only in the orientation of one chiral center.Draw the enantiomers of 2-methyloxirane
