Draw a structural formula of the S configuration of the compound shown below.
The specific rotation, [α]D, for (-)-malic acid is -27. What is the observed rotation for a solution of 0.50 g of (-)-malic acid in 10 mL of water in a sample tube having a pathlength of 10 cm?
The observed rotation of a solution of 0.75 g of a compound in 10 mL of water is -4.6 degrees. If the pathlength is 10 cm, what is the specific rotation of the compound?
The observed rotation of a solution of 1.4 g of a compound in 10 mL of water is +1.3 degrees. If the pathlength is 10 cm, what is the specific rotation of the compound?
Draw a structural formula of the S configuration of the compound shown below. The specific rotation,...
The specific rotation, (a)p, for (+)-alanine is +8.5. What is the observed rotation for a solution of 1.7 g of (+)-alanine in 10 mL of water in a sample tube having a pathlength of 10 cm? degrees The observed rotation of a solution of 1.3 g of a compound in 10 mL of water is +8.2 degrees. If the pathlength is 10 cm, what is the specific rotation of the compound? The specific rotation, (a)p, for(-)-pseudoephedrine is - 52. What...
The specific rotation, [a]D, for (-)-pseudoephedrine is-52. What is the observed rotation for a solution of 0.50 g of (-)- pseudoephedrine in 10 mL of water in a sample tube having a pathlength of 10 cm? degrees The observed rotation of a solution of 1.7 g of a compound in 10 mL of water is +13 degrees. If the pathlength is 10 cm, what is the specific rotation of the compound? Submit Answer Retry Entire Group No more group attempts...
5.41 Predict the value for the specific rotation of the following compound. Explain your answer. -OH НО. 5.42 The specific rotation of (S)-2-butanol is +13.5. If 1.00 g of its enantiomer is dissolved in 10.0 mL of ethanol and placed in a sample cell with a length of 1.00 dm, what observed rotation do you expect? 5.43 The specific rotation of l-alanine in water (at 25°C) is +2.8. A chemist prepared a mixture of l- alanine and its enantiomer, and...
The specific rotation [α] of (1S, 2R)-ephedrine HCl salt in water is −32.5° at 22 °C (light source: sodium D line). What is the optical rotation α in degrees (°) of an aqueous solution containing 250 mg/mL (1R, 2S)-ephedrine HCl salt AND 50 mg/mL (1S, 2R)-ephedrine HCl salt measured using a 1.00-cm pathlength tube under the same condition?
Draw a structural formula of the S configuration of the compound shown below. Draw a structural formula of the S configuration of the compound shown below. Draw the products of the reaction shown. Electron flow is indicated with curved arrows. H2N NH2 -CH2C1 H₃C CH₂
Draw a structural formula of the RS configuration of the compound shown below. Draw a structural formula of the RS configuration of the compound shown below. OH HO OH CHCH,O ascorbic acid . Use the wedge/hash bond tools to indicate stereochemistry Include H atoms at chiral centers only If a group is achiral, do not use wedged or hashed bonds on it.
D Apure stereoisomer of a compound has a specific rotation Of - 39.00. A 100 ML solution of o.187 g ot an enantiomeric mixture of the compound has an Obschied rotation of -6.520 When placed in a polanmeter tube 10cm long. what is the percent of each enantiomer in the solution? Show all work." ort Answer: Answer each question to the best of your ability. Be sure to show your thought udget your time wisely - not all questions are...
? What is the enantiomeric excess of an adrenaline sample that has a specific rotation of - 47.7? pure adrenaline has a specific rotation of -53, 4 pts 0) The observed rotation of 4.0 grams of compound in a 40 ml of a solution in a polarimeter Tube 20 cm dong is + 14.40 What is the specific rotation of the compound. 4 pts. Idm = 100m [a] E d Сх
Draw a structural formula of the RR configuration of the compound shown below.Use the wedge/hash bond tools to indicate stereochemistry where it exists.Include H atoms at chiral centers only.If a group is achiral, do not use wedged or hashed bonds on it.Thanks
7 (7 pts) The specific rotation, (a), of an optically pure natural product 15 compound we made in the lab was prepared by diluting 12.55 grams of it in a 30.0 cm polarimeter tube. pure natural product is -65.0°. A sample of the same uuting 12.55 grams of it into 40.0 ml of ethanol and placed A) Our compound was found to have an "ee" of 80% - What was the specific totam % - What was the specific rotation...