EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
6th Edition
ISBN: 9781305687875
Author: Gilbert
Publisher: CENGAGE LEARNING - CONSIGNMENT
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Question
Chapter 3.2, Problem 17E
Interpretation Introduction
Interpretation:Solvents or mixture of solvents that can be considered for recrystallization of solids A and b should be explained.
Concept introduction:Criteria mentioned below should be used to select solvent for recrystallization.
1. Solvent should be able to dissolve desired compound in itself at high temperatures but insoluble at low temperatures. In short, solvent with favorable temperature coefficient should be used for particular solute.
2. Solvent should be chosen in such way that impurities are either insoluble in it or remain moderately soluble in it at low temperatures.
3. Boiling point of desired solvent should be low so that it gets separated from crystals easily.
4. Boiling point of solvent should be less than melting point of solid under consideration.
5. There should be no reaction between solvent and substance that needs to be purified.
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Students have asked these similar questions
2. When performing the recrystallization of an impure solid, why is it advised to use the minimal amount of solvent possible?
Group of answer choices
To minimize the amount of pure solid lost due to its solubility.
To minimize the cost of the recrystallization.
To reduce the time needed to filter the pure solid from the solvent after recrystallization.
To minimize the amount of hazardous materials used.
Just because there appears to be a good match between solubility characteristics between solute and solvent doesn’t mean you’ve found a good system. For example, benzyl alcohol appears to have favorable solubility characteristics with fluorenol, but it is a poor choice of solvent. Explain why this might be.
It is important that the correct solution is used for rinsing volumetric glassware. Discuss how your results would be affected if you had used the wrong solutions to rinse the glassware. Briefly explain your answers.
Chapter 3 Solutions
EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
Ch. 3.2 - Prob. 1ECh. 3.2 - Prob. 2ECh. 3.2 - Prob. 3ECh. 3.2 - Prob. 4ECh. 3.2 - Prob. 5ECh. 3.2 - Prob. 6ECh. 3.2 - Prob. 7ECh. 3.2 - Prob. 8ECh. 3.2 - Prob. 9ECh. 3.2 - Prob. 10E
Ch. 3.2 - Prob. 11ECh. 3.2 - Prob. 12ECh. 3.2 - Prob. 13ECh. 3.2 - Prob. 14ECh. 3.2 - Prob. 15ECh. 3.2 - Prob. 16ECh. 3.2 - Prob. 17ECh. 3.2 - Prob. 18ECh. 3.2 - Prob. 19ECh. 3.2 - Prob. 20ECh. 3.2 - Prob. 21ECh. 3.2 - Prob. 22ECh. 3.2 - Prob. 23ECh. 3.2 - Prob. 24ECh. 3.2 - Prob. 25ECh. 3.2 - Prob. 26ECh. 3.2 - Prob. 27ECh. 3.2 - Prob. 28ECh. 3.2 - Prob. 29ECh. 3.2 - Prob. 30ECh. 3.2 - Prob. 31ECh. 3.2 - Prob. 32ECh. 3.2 - Prob. 34ECh. 3.3 - Prob. 1ECh. 3.3 - Prob. 2ECh. 3.3 - Prob. 3ECh. 3.3 - Prob. 4ECh. 3.3 - Prob. 5ECh. 3.3 - Prob. 6ECh. 3.3 - Prob. 7ECh. 3.3 - Prob. 8ECh. 3.3 - Prob. 10ECh. 3.3 - Prob. 11ECh. 3.3 - Prob. 12ECh. 3.3 - Prob. 13ECh. 3.3 - Prob. 14ECh. 3.3 - Prob. 15ECh. 3.3 - Prob. 16ECh. 3.3 - Prob. 17ECh. 3.3 - Prob. 18ECh. 3.3 - Prob. 19ECh. 3.3 - Prob. 21ECh. 3.3 - Prob. 22ECh. 3.3 - Prob. 23ECh. 3.3 - Prob. 24ECh. 3.3 - Prob. 25ECh. 3.3 - Prob. 26E
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