Organic Chemistry Question
Calculate the optical activity of a sample if it has 34% R, and 76% S-glutamic acid with a specific rotation of (-)8.9° for the R isomer.
Organic Chemistry Question Calculate the optical activity of a sample if it has 34% R, and...
2. The optical activity, measured by specific rotation, of pure (R-malic acid is [a]20D-+27% What is the specific rotation of a mixture of 50% and 50% of (R)-malic acid and (S)-malic acid? What is enantiomeric excess of a sample of malic acid containing both enantiomers that has a [al20D -0% [a]20D-27"; [a]20D-_ 13.5": [a]20D-+ 13.5°
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...
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...
repared a limonene sample with a concentration of 0.044 g/mL and measured an optical rotation of a=8.78 degrees using a 20 cm polarimeter tube. Calculate the specific rotation () of the students limonene sample and write your answer in the box. (review Example 1 in the procedure for how to do this) 6. If a mixture of (R) and (S)-Limonene Acid gives a %ee of 80.35% favoring the R enantiomer, use this to calculate the ratio of R to S...
If a pure R isomer has a specific rotation of – 106.0°, and a sample contains 79.0% of the R isomer and 21.0% of its enantiomer, what is the observed specific rotation of the mixture? Number [a] = 10
If a pure R isomer has a specific rotation of –136.0°, and a sample contains 65.0% of the R isomer and 35.0% of its enantiomer, what is the observed specific rotation of the mixture?
if a pure R isomer has a specific rotation of -106.0, and a sample contains 70.0% of the R isomer and 30.0% of it's enantiomer, what is the observed specific rotation of the mixture
(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
A sample of limonene has a specific rotation of +71.3 R-(+)-limonene [dD = + 125.6" and, S-(-)-limonene [a]D--1 22. 1 ®. What is the % ee? Number %ee What is the molecular composition of this same sample? Number s isomer = 1 % 1Somer Number R isomer-
1. Percent Enantiomerie Excess (ee) is given by the equation if in moless (The difference between Rand S isomers/sum of R & S isomer) - 100. Thus, the sample prepared by Dr. Z. Evans in the PSB 340 Lab contained 12.8 moles of isomer and 3.2 moles of the S isomer. a. Which isomer is in excess in Dr. Evans product? 3.2 moles b. By how much: 12.8 - 3.2 x100 c. What is the percent ce? 2. Enantiomeric Excess...