Part of a stereochemistry and polarimetry lab
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Part of a stereochemistry and polarimetry lab 3. (4pts) (S)-2-bromobutane has a reported specific rotation of...
9. Specific rotation of enantiopure (R)-malic acid is -6. An unknown sample was found to have a specific rotation of -2 Which isomer is the major component in the unknown mixture? HO OH Malic Acid O OH Circle one: R S What is the enantiomeric excess of the mixture? Show your calculations. 9. Specific rotation of enantiopure (R)-malic acid is -6. An unknown sample was found to have a specific rotation of -2 Which isomer is the major component in...
(s)-7-chbrobota 3. (2 points) Consider that (S)-2-Chlorobutane has a specific rotation of +13.1 and (R)-2-Chlorobutane has a specific rotation of -13.1 °. Which isomer is dominant and what is the optical purity of the mixture of (R) and (S)-2- Chlorobutane, whose specific rotation was found to be -2.5°. What is the percent composition of the mixture? ile there iture La
11. (R)-2-bromooctane has a specific rotation of -34.25° and (S)-2-octanol has a specific fola +9.90*. If an 80/20 mixture of (R)-2-bromooctane and (S)-2-bromooctane undergoes DN HO", what will be the specific rotation of the product? Br ОН NaOH
3. Diastereomers and Meso Forms. When a molecule has two or more stereogenic centers, stereoisomers that are not mirror images can exist; these are called diastereoisomers. Within this general class, there are special types of stereoisomers that are always optically inactive and are called meso forms. Construct a model with four different colored balls about a carbon center. Construct another identical to the first and verify this by the superimposition test. Now remove the same colored balls, blue (C from...
Please help with pre-lab questions. Pre-Lab Questions: 1. A sample of 2-butanol has a specific rotation of +3.25. Determine the optical purity (%ee) and percent composition of this sample (see Mohrig section 17.4). The specific rotation of pure (+)-2-butanol is +13.0°. 2. The equation for the formation of the diastereomeric salts is shown in the background information (performed in Part A of the procedure). Write this chemical equation in your notebook, then ALSO write a balanced equation for the formation...