Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 5, Problem 5.30P
Interpretation Introduction
Interpretation:
Measured angle of rotation for penicillin V is to be calculated.
Concept introduction:
Measured angle of rotation is the angle by which, “the chiral compound rotates the plane-polarized light”. The formula for it is:
Where
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
The specific rotation, [a], for (-)-pseudoephedrine is -52. What is the observed rotation for a solution of 0.70 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 1.2 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?
The specific rotation of vitamin C ( using the D line of sodium, at 20°C) is +24. Predict what the observed rotation would be for a solution containing 0.100 g of vitamin C dissolved in 10.0 ml of ethanol and placed in a sample cell with a length of 1dm.
2. The observed rotation of a compound, X (14.0g dissolved in water to make 100ml. of solution) in a polarimeter
tube of length 30cm is +10.5°. What is the specific rotation of X?
Chapter 5 Solutions
Organic Chemistry: Principles and Mechanisms (Second Edition)
Ch. 5 - Prob. 5.1PCh. 5 - Prob. 5.2PCh. 5 - Prob. 5.3PCh. 5 - Prob. 5.4PCh. 5 - Prob. 5.5PCh. 5 - Prob. 5.6PCh. 5 - Prob. 5.7PCh. 5 - Prob. 5.8PCh. 5 - Prob. 5.9PCh. 5 - Prob. 5.10P
Ch. 5 - Prob. 5.11PCh. 5 - Prob. 5.12PCh. 5 - Prob. 5.13PCh. 5 - Prob. 5.14PCh. 5 - Prob. 5.15PCh. 5 - Prob. 5.16PCh. 5 - Prob. 5.17PCh. 5 - Prob. 5.18PCh. 5 - Prob. 5.19PCh. 5 - Prob. 5.20PCh. 5 - Prob. 5.21PCh. 5 - Prob. 5.22PCh. 5 - Prob. 5.23PCh. 5 - Prob. 5.24PCh. 5 - Prob. 5.25PCh. 5 - Prob. 5.26PCh. 5 - Prob. 5.27PCh. 5 - Prob. 5.28PCh. 5 - Prob. 5.29PCh. 5 - Prob. 5.30PCh. 5 - Prob. 5.31PCh. 5 - Prob. 5.32PCh. 5 - Prob. 5.33PCh. 5 - Prob. 5.34PCh. 5 - Prob. 5.35PCh. 5 - Prob. 5.36PCh. 5 - Prob. 5.37PCh. 5 - Prob. 5.38PCh. 5 - Prob. 5.39PCh. 5 - Prob. 5.40PCh. 5 - Prob. 5.41PCh. 5 - Prob. 5.42PCh. 5 - Prob. 5.43PCh. 5 - Prob. 5.44PCh. 5 - Prob. 5.45PCh. 5 - Prob. 5.46PCh. 5 - Prob. 5.47PCh. 5 - Prob. 5.48PCh. 5 - Prob. 5.49PCh. 5 - Prob. 5.50PCh. 5 - Prob. 5.51PCh. 5 - Prob. 5.52PCh. 5 - Prob. 5.53PCh. 5 - Prob. 5.54PCh. 5 - Prob. 5.55PCh. 5 - Prob. 5.56PCh. 5 - Prob. 5.57PCh. 5 - Prob. 5.58PCh. 5 - Prob. 5.59PCh. 5 - Prob. 5.60PCh. 5 - Prob. 5.61PCh. 5 - Prob. 5.62PCh. 5 - Prob. 5.63PCh. 5 - Prob. 5.64PCh. 5 - Prob. 5.65PCh. 5 - Prob. 5.66PCh. 5 - Prob. 5.67PCh. 5 - Prob. 5.68PCh. 5 - Prob. 5.69PCh. 5 - Prob. 5.70PCh. 5 - Prob. 5.71PCh. 5 - Prob. 5.72PCh. 5 - Prob. 5.73PCh. 5 - Prob. 5.74PCh. 5 - Prob. 5.75PCh. 5 - Prob. 5.76PCh. 5 - Prob. 5.77PCh. 5 - Prob. 5.78PCh. 5 - Prob. 5.79PCh. 5 - Prob. 5.1YTCh. 5 - Prob. 5.2YTCh. 5 - Prob. 5.3YTCh. 5 - Prob. 5.4YTCh. 5 - Prob. 5.5YTCh. 5 - Prob. 5.6YTCh. 5 - Prob. 5.7YTCh. 5 - Prob. 5.8YTCh. 5 - Prob. 5.9YTCh. 5 - Prob. 5.10YTCh. 5 - Prob. 5.11YTCh. 5 - Prob. 5.12YTCh. 5 - Prob. 5.13YTCh. 5 - Prob. 5.14YTCh. 5 - Prob. 5.15YTCh. 5 - Prob. 5.16YTCh. 5 - Prob. 5.17YT
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.Similar questions
- 1. When 0.247 g of monosodium glutamate (MSG) is dissolved in 10.0 mL of water and placed in a sample cell 10.0 cm in length, the observed rotation at 20°(using the D line of sodium) is +0.632°. Calculate the specific rotation of MSG. 2. When 0.095 g of cholesterol is dissolved in 1.00 mL of ether and placed in a sample cell 10.0 cm in length, the observed rotation at 20°C (using the D line of sodium) is -0.299°.Calculate the specific rotation of cholesterol.3. The specific rotation of L-dopa in water (at 15°C) is -39.5. A chemist prepared a mixture of L-dopa and its enantiomer, and this mixture had a specific rotation of -34. Calculate the % ee of this mixture. 4. The specific rotation of vitamin B7 in water (at 22°C) is +92. A chemist prepared a mixture of vitamin B7 and its enantiomer, and this mixture had a specific rotation of +18. Calculate the % ee of this mixture.arrow_forwardPlease answer the question in the picture that is attached. thank you so much :)arrow_forwardConsider a solution that contains 74.0% R isomer and 26.0% S isomer. If the observed specific rotation of the mixture is -45.0°, what is the specific rotation of the pure R isomer? [a] =arrow_forward
- stereochemistry question: Calculate the specific rotations of the following samples taken at 25 °C using the sodium D line. (a) 1.00 g of sample is dissolved in 20.0 mL of ethanol. Then 5.00 mL of this solution is placed in a 20.0-cm polarimeter tube. The observed rotation is 1.25° counterclockwise. (b) 0.050 g of sample is dissolved in 2.0 mL of ethanol, and this solution is placed in a 2.0-cm polarimeter tube. The observed rotation is clockwise 0.043°. refer to the question belowarrow_forwardHow can we decide whether an observed rotation of a solution of an optically active compound is +170° and not actually -190°?arrow_forwardThe 4th problemarrow_forward
- Question2 Show all Steps Assume that the following measurements are made in 10cm. polarimeter Sample containers: (1) A 10ml Solution of 0.49 of optically active 2-butanol in water displays an optical rotation of -0.56. What is its specific rotation? (ii) A Solution of pure (S) 2-bromobutane in ethanol is found to have an observed rotation α= 57-3°, if [cc) for (S) 2-bromobutane is +23-1, what is the concentration of the Solution?arrow_forwarde) Acetaminophen Exp: -NH2 Ноarrow_forwarda) Draw structural formulas for the two monosaccharides that result when structure III istreated as shown below. (b) Draw the monosaccharide that results when product A from the previous step (Q1a) istreated with Br2/H2O. (c) Draw the monosaccharide that results when product A from the previous step (Q1a) istreated with 1.NaBH4 / 2. H2O.arrow_forward
- R Question) Draw the following by the Chemdraw and write the Molar Mass? 1-Amino-3-bromonaphthalene (3-bromo-a-naphthylamine) 8-Aminoquinoline 2-Nitroaniline 3,4-Diaminotriphenylmethane 4-Chloroaniline 4-Aminophenylurethanearrow_forwardIV) Biomolecules - Below are examples of three classes of biomolecules we will not discuss in this class: OH What is the R/S configuration of the indicated carbon? H. Circle one: More soluble in. Water Нехane HO Circle the most acidic proton (if it is not shown, draw it in and circle it). estrogen (lipid) NH2 How many stereocenters does this tripeptide have? Circle one: Is the circled functional group aromatic? YES NO H2N What is the Index of Hydrogen Deficiency of this peptide? NH A tripeptide (three amino acids) Name the circled functional group: What is the hybridization of the indicated oxygen? (CH2)16CH3 Circle one: Is this triacylglyceride optically active? YES NO H3C(H2C)16' Circle one: More soluble in... Water Oil -(CH2)16CH3 Explain why the triacylglyceride is more soluble in your choice above: a triacylglyceridearrow_forwardThe figure can rotate the plane of polarized light by 4.52 counterclockwise, 1. what is its configuration based on optical activity, 2. what is the absolute and relative configuration of the figure and 3. what is the angle of rotation of the plane-polarized light of its ENANTIOMERarrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning