Essential Organic Chemistry, Global Edition
3rd Edition
ISBN: 9781292089034
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Question
Chapter 4.8, Problem 24P
(a)
Interpretation Introduction
Interpretation:
The rotation of R-lactic acid has to be predicted.
Concept introduction:
Enantiomer has asymmetric centers, so it shows optical activity.
If Enantiomer that rotates plane polarized light in counterclockwise direction, then it is called levorotatory.
If Enantiomer that rotates plane polarized light in clockwise direction, then it is called dextrorotatory.
Pair of enantiomers has different optical activity, which means if one will show levorotatory then the other will show dextrorotatory.
(b)
Interpretation Introduction
Interpretation:
The rotation of R-sodium lactate has to be predicted.
Concept introduction:
Enantiomer has asymmetric centers, so it shows optical activity.
If Enantiomer that rotates plane polarized light in counterclockwise direction, then it is called levorotatory.
If Enantiomer that rotates plane polarized light in clockwise direction, then it is called dextrorotatory.
Pair of enantiomers has different optical activity, which means if one will show levorotatory then the other will show dextrorotatory.
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1. This experiment is more about understanding the colligative properties of a solution rather than the determination of
the molar mass of a solid.
a. Define colligative properties.
b. Which of the following solutes has the greatest effect on the colligative properties for a given mass of pure water?
Explain.
(i) 0.01 mol of CaCl2
(ii) 0.01 mol of KNO3
(iii) 0.01 mol of CO(NH2)2
(an electrolyte)
(an electrolyte)
(a nonelectrolyte)
5. b. For Trials 2 and 3, the molar mass of the solute was 151 g/mol and 143 g/mol respectively.
a. What is the average molar mass of the solute ?
b. What are the standard deviation and the relative standard deviation (%RSD) for the molar mass of the solute ?
Show work. Don't give Ai generated solution
Chapter 4 Solutions
Essential Organic Chemistry, Global Edition
Ch. 4.1 - Draw the cis and trans isomers for the following:...Ch. 4.1 - Prob. 4PCh. 4.1 - Prob. 5PCh. 4.1 - Prob. 6PCh. 4.2 - Prob. 7PCh. 4.2 - Tamoxifen slows the growth of some breast tumors...Ch. 4.2 - Draw and label the E and Z isomers for each of the...Ch. 4.2 - Prob. 10PCh. 4.2 - Name each of the following:Ch. 4.2 - Draw the structure of (Z)-2,3-dimethyl-3-heptene.
Ch. 4.3 - Prob. 13PCh. 4.4 - Prob. 14PCh. 4.5 - Prob. 16PCh. 4.6 - Prob. 17PCh. 4.7 - Assign relative priorities to the groups or atoms...Ch. 4.7 - Name the following:Ch. 4.7 - Prob. 22PCh. 4.7 - Draw a perspective formula for each of the...Ch. 4.8 - Prob. 24PCh. 4.8 - Prob. 27PCh. 4.9 - Prob. 28PCh. 4.9 - Prob. 29PCh. 4.9 - Prob. 30PCh. 4.10 - Prob. 31PCh. 4.10 - Prob. 32PCh. 4.10 - Prob. 33PCh. 4.11 - Prob. 34PCh. 4.11 - a. Draw the stereoisomers of...Ch. 4.11 - Prob. 37PCh. 4.11 - Prob. 38PCh. 4.12 - Which of the following compounds has a...Ch. 4.12 - Draw all the stereoisomers for each of the...Ch. 4.12 - Limonene exists as two different stereoisomers....Ch. 4 - a. Draw three constitutional isomers with...Ch. 4 - Which of the following have an asymmetric center?...Ch. 4 - Prob. 45PCh. 4 - Prob. 46PCh. 4 - Of all the possible cyclooctanes that have one...Ch. 4 - Prob. 48PCh. 4 - Prob. 49PCh. 4 - Prob. 50PCh. 4 - Prob. 51PCh. 4 - Prob. 52PCh. 4 - Draw the stereoisomers of 2,4-dichlorohexane....Ch. 4 - Prob. 54PCh. 4 - Prob. 55PCh. 4 - Prob. 56PCh. 4 - Prob. 57PCh. 4 - Prob. 58PCh. 4 - Prob. 59PCh. 4 - Prob. 60PCh. 4 - Prob. 61PCh. 4 - Prob. 62PCh. 4 - Draw structures for each of the following: a....Ch. 4 - Prob. 64PCh. 4 - a. Draw all the isomers with molecular formula...Ch. 4 - Prob. 66PCh. 4 - Prob. 67PCh. 4 - Prob. 68PCh. 4 - Chloramphenicol is a broad-spectrum antibiotic...
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