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A: Option A is correct answer R.
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- If the sample of the pure R enantiomer of a molecule has a specific rotation of -40 degrees and your mixture of that molecule has an 82% ee S, what is the observed specific rotation of your sample?Assign R and S to all of the asymmetric centers in the following molecules.Which Carbons are chiral? What is the absolute (R/S) configuration of the chiral carbon that IS NOT also part of a ring? Is it an R or S configuration? Show the priorities the using the structure below that led to this answer.
- Name the following and include any E/Z stereochem in the name .a. The specific rotation for pure R is +5.0, what percentage of the mixture is R when the observed roation is -2.0. b. The rotation for pure S=-100. What is the observed rotation of a mixture that is 20%S and 80%R? I need an easy way to solve these kinds of problem, please!!For the molecules below, assign the stereocenter’s absolute configuration as R or S
- 1.What is the absolute configuration of this isomer of 2,3-dihydroxybutanal? pls explain.2. What is the absolute configuration of the enantiomer of the isomer?In each case, assign the correct configuration of R or S, 1 is highest priority, 4 is lowest priority.For bromochloromethanol that has R configuration Interchange any 2substituent, what is the absolute r/s configuration?
