Homework Answers
- Option D , Enantiomer pair will have same optical rotation but opposite sign of rotation.
- Enantiomers are optical isomers and are non super impossable mirror images of each other .
- The optical rotation of both the isomers will be same in magnitude. But have opposite sign of rotation. One isomer rotates palne polarized light clockwise and other rotates anticlockwise.
- So the optical rotation of one isomer of enantiomer pair is -109.8o , the optical rotation of the other enantiomer would be +109.8o
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optical activity problems.. please show all steps i dont
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A 0.110 M solution of an enantiomerically pure chiral compound D has an observed rotation of +0.24° in a 1-dm sample container. The molar mass of the compound is 144.0 g/mol. (a) What is the specific rotation of D? (b) What is the observed rotation if this solution is mixed with an equal volume of a solution that is 0.110 M in L, the enantiomer of D? Number deg mL Number g dm deg (c) What is the observed rotation...
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1) Suppose that a pure compound has a specific rotation of +49°. In the laboratory a solution in which the compound is mixed with its enantiomer is found to have a specific rotation of +12. What is the %ee of the mixture? What percent of the mixture is (+) enantiomer and what percent is (-) enantiomer? 2) Give the structure of 3,3-Dimethylpetane. How many monochlorinated product can be formed from this compound reacting with Cl? Give the structure of each...
2) Natural epinephrine (with a specific rotation of -50°) is used medicinally. Its enantiomer is medically worthless and is, in fact, toxic. You, a pharmacist, are given a solution said to contain epinephrine, but the optical purity is not mentioned. You place it in a polarimeter and get an observed optical rotation of -150. What is the enantiomeric excess of natural epinephrine? How much of each enantiomer is in the mixture? You must show your work to get credit.
optical activity problems.. please show all steps i dont
understand
You have a sample (Sample X) which is a mixture of +/- Carvone. The solution was made by dissolving 4.50 g of the sample in enough methanol to bring the volume of solution to 10,0 ml. Some of the solution is placed in a 100 cm polarimeter cell and its optical rotation is measured at 25°C using light of the sodium D line wavelength (589.6 nm). The observed rotation is...
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