EBK EXPERIMENTAL ORGANIC CHEMISTRY: A M
6th Edition
ISBN: 9781305687875
Author: Gilbert
Publisher: CENGAGE LEARNING - CONSIGNMENT
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 3.2, Problem 18E
Interpretation Introduction
Interpretation:Separation of mixture of sand and benzoic acid to have pure benzoic acid should be explained.
Concept introduction:Recrystallization is technique that is used for purification of organic compounds. This process includes dissolution of solid in specific solvent at high temperature and then crystals are made again by process of cooling. Temperature of crystals is decreased to allow impurities to remain in solution only.
Expert Solution & Answer
Trending nowThis is a popular solution!
Students have asked these similar questions
What is the solubility of benzoic acid in water at 10 degrees celcius?
Explain the difference in the solubility of benzoic acid and sodium benzoate in water.Which of the two would you predict to be more soluble in CHCl3? Explain.
Compare the three main purification methods (recrystallization, distillation, and extraction) by stating whateach one is best for.
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
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
- What is the difference in the solubility of benzoic acid and sodium benzoate in water and explain which of them will be more soluble in chloroform.arrow_forward3 ways to separate alcohol to a liquid mixture and its step by step procedurearrow_forwardYou have a mixture of an aryl halide and a carboxylic acid that you wish to separate (both are solids). Both are soluble in diethyl ether. Explain ALL the steps you would take to obtain the two compounds in pure form from your sample.arrow_forward
- You have a mixture of an aryl halide and a carboxylic acid that you wish to separate(both are solids). Both are soluble in diethyl ether. Explain ALL the steps you would take to obtain the two compounds in pure form from your sample.arrow_forward16-18 Choose the letter of the correct answer.arrow_forward1-propanol, 2-propanol, and 1-butanol all have boiling too close together to be separated using the simple distillation column. What equipment be used to separate a mixture of these three?arrow_forward
- 1. What boiling point of the following mixture of compounds. Then, which would boil first? And Finally, indicate what type of distillation will you use to separate them.arrow_forwardWhy is benzoic acid insoluble in sulfuric acid? Explain the conceptarrow_forwardThe mixture contains benzoic acid, 2-napthol, and naphthalene. Dissolve the mixture in the polar solvent ether. When you react the mixture with 10% NaHCO3(sodium bicarbonatea weak base in aqueous solution) reacts with benzoic acid and forms sodium benzoate an ionic compound (similar to NaCl) that dissolves in aqueous solution (heavier than ether in density) and goes to the bottom of the centrifuge tube or to the bottom of the separatory funnel forming two layers. Then remove the bottom aqueous layer and collect in a beaker labeled as bicarbonate extract. Acidify the bicarbonate extract in the beaker to give benzoic acid. The top ethereal layer contains in the centrifuge tube or separatory funnel 2-napthol and naphthalene. To this top layer add 10% NaOH (sodium hydroxideis a strong base in aqueous solution reacts with only 2-napthol, a weak acid forming 2-napthoxide an ionic compound soluble in aqueous solution (similar to NaCl) that goes to the bottom of the centrifuge tube or to…arrow_forward
- Draw a scheme to show how one would separate a mixture of naphthalene and aniline (Hint: aniline is an organic base that reacts with HCl(aq) to form a salt).arrow_forwardTable 1. Solubility Tests. Functional Group Observations (specify type if any) Sample in concentrated (+/-) H2SO4 Color orange Hydroxyl group Hydroxyl group Hydroxyl group 1-butanol Color orange 2-butanol Color orange diisopropyl ether Look at the structures of compounds tested for solubility in concentrated H2SO4. What generalization can be made for a substance to be soluble in concentrated H2SO4 ?arrow_forwarda) Succinimide is an organic compound used in manysyntheses as a building block and is related to a class of drugs known asanticonvulsants. Given the following solubility of succinimide in water andmethanol, which would be a better solvent for recrystallizing succinimide?Solubility data: 1 gram of succinimide is soluble in 5 mL of cold water, 3 mL ofwater at room temperature and 0.7 mL of boiling water. 1 gram of succinimide issoluble in 30 mL of cold methanol, 24 mL of room temperature methanol and 5mL of hot methanol. Show calculations.b) A researcher wanted to purify 0.4 grams of crude succinimide viarecrystallization using only 2 mL of solvent. Decide the best solvent to use (water or methanol) to show the maximum % recovery of the researcher. The best solvent chosen here, may differ from the one chosen in part a. PLEASE show calculations for both parts as proof.arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
EBK A SMALL SCALE APPROACH TO ORGANIC LChemistryISBN:9781305446021Author:LampmanPublisher:CENGAGE LEARNING - CONSIGNMENT
Chemistry: Matter and ChangeChemistryISBN:9780078746376Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl WistromPublisher:Glencoe/McGraw-Hill School Pub Co
Chemistry: The Molecular ScienceChemistryISBN:9781285199047Author:John W. Moore, Conrad L. StanitskiPublisher:Cengage Learning
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
EBK A SMALL SCALE APPROACH TO ORGANIC L
Chemistry
ISBN:9781305446021
Author:Lampman
Publisher:CENGAGE LEARNING - CONSIGNMENT
Chemistry: Matter and Change
Chemistry
ISBN:9780078746376
Author:Dinah Zike, Laurel Dingrando, Nicholas Hainen, Cheryl Wistrom
Publisher:Glencoe/McGraw-Hill School Pub Co
Chemistry: The Molecular Science
Chemistry
ISBN:9781285199047
Author:John W. Moore, Conrad L. Stanitski
Publisher:Cengage Learning
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning