Systematic Identification of Organic Compounds, Student Solutions Manual (eBook)
256 Seiten
Wiley (Verlag)
978-1-119-79992-4 (ISBN)
The Student Solutions Manual to accompany The Systematic Identification of Organic Compounds, 9th Edition is an essential resource for any student using the parent text in class. Providing complete solutions to all practice problems provided in the textbook, this book allows you to assess your understanding of difficult material and clarify complex topics. Fully aligned with the text, this book details structures, formulas, mechanisms, and more to help you pinpoint areas of difficulty and focus your study time for more efficient learning.
Preface vii
Chapter 4 Preliminary Examination, Physical Properties, and Elemental Analysis 1
Chapter 5 Classification of Organic Compounds by Solubility 5
Chapter 6 Separation of Mixtures 13
Chapter 7 Nuclear Magnetic Resonance Spectrometry 23
Chapter 8 Infrared Spectrometry 45
Chapter 9 Mass Spectrometry 51
Chapter 10 Chemical Tests for Functional Groups 55
Chapter 11 The Preparation of Derivatives 73
Chapter 13 Structural Problems 117
Problem Set 1 117
Problem Set 2 120
Problem Set 3 144
Problem Set 4 166
Problem Set 5 169
Problem Set 6 172
Problem Set 7 178
Problem Set 8 183
Problem Set 9 188
Problem Set 10 192
Problem Set 11 197
Problem Set 12 203
Problem Set 13 207
Problem Set 14 211
Problem Set 15 218
Problem Set 16 224
Problem Set 17 228
Problem Set 18 232
Problem Set 19 237
Problem Set 20 242
Chapter 5
Classification of Organic Compounds by Solubility
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- N – alcohols, aldehydes, ketones, esters with one functional group and more than five but fewer than nine carbons, ethers, epoxides, alkenes, alkynes, some aromatic compounds (especially those with activating groups).
- S1 – monofunctional alcohols, aldehydes, ketones, esters, nitriles, and amides with five carbons or fewer.
- A2 – weak organic acids; phenols, enols, oximes, imides, sulfonamides, thiophenols, all with more than five carbons; β‐diketones; nitro compounds with α‐hydrogens.
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- Insoluble in water, soluble in 5% sodium hydroxide solution, soluble in 5% sodium bicarbonate solution.
- Soluble in water and ether, litmus paper turned blue.
- Insoluble in water, 5% sodium hydroxide solution, and 5% hydrochloric acid solution, but soluble in 96% sulfuric acid solution.
- Soluble in water and ether; litmus paper is unchanged in color.
- Soluble in water and ether; litmus paper is unchanged in color.
- Insoluble in water and 5% sodium bicarbonate solution, but soluble in 5% sodium hydroxide solution.
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- A1
- SB
- N
- S1
- S1
- A2
- Both acyl halides and anhydrides react with water, so any results would be of the carboxylic acid that is formed from the hydrolysis of these compounds.
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- 1‐Propanol is more soluble in water than diethyl ether. 1‐Propanol can hydrogen bond with water, whereas diethyl ether does not hydrogen bond with water.
- Pentanedioic acid is more soluble in water than butanedioic acid. Odd carbon number of dioic acids have less intracrystalline forces than even carbon number of dioic acids.
- Methyl methacrylate is more soluble in water than poly(methyl methacrylate). Polymers are insoluble in water.
- Butanoic acid is more soluble in water than 2‐Bromobutanoic acid. The addition of halogens increases the molecular weight and decreases the solubility.
- 2‐Methylpropanoic acid is more soluble in water than butanoic acid. Branching lowers the boiling point and lowers intermolecular forces. Thus, a branched compound is more soluble in water than a straight chain molecule.
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- 1‐Chlorobutane is insoluble in water since it is an haloalkane. It is insoluble in 5% sodium hydroxide solution, 5% hydrochloric acid solution, and 96% sulfuric acid solution. Thus 1‐Chlorobutane is in solubility class I.
- 4‐Methylaniline is insoluble in water since it is an aniline. It is basic, due to the presence of the amino group, and therefore is insoluble in 5% sodium hydroxide solution, but soluble in 5% hydrochloric acid solution, and thus 4‐methylaniline is in solubility class B.
- 1‐Nitroethane is insoluble in water since it is a weak organic acid. It is soluble in 5% sodium hydroxide solution, but insoluble in 5% sodium bicarbonate solution, and thus 1‐nitroethane is in solubility class A2.
- Alanine is an amino acid, thus is amphoteric, and soluble in water. Alanine is insoluble in ether and thus in solubility class S2.
- Benzophenone is insoluble in water because it has more than five carbon atoms. Since it is a neutral compound, containing only carbon, hydrogen, and oxygen, it is insoluble in water, 5% sodium hydroxide solution, and 5% hydrochloric acid solution. It is soluble in 96% sulfuric acid solution. Therefore, benzophenone is in solubility class N.
- As a strong organic acid, benzoic acid is insoluble in water, soluble in 5% sodium hydroxide solution, and soluble in 5% sodium bicarbonate solution. Therefore, benzoic acid is in solubility class A1.
- As a saturated hydrocarbon, hexane is insoluble in water, 5% sodium hydroxide solution, 5% hydrochloric acid solution, and 95% sulfuric acid. Hexane is in solubility class I.
- 4‐Methylbenzyl alcohol is insoluble in water since it has more than five carbon atoms. It is a neutral compound with only carbon, hydrogen, and oxygen. It is insoluble in water, 5% sodium hydroxide solution and 5% hydrochloric acid solution. However, 4‐methylbenzyl alcohol is soluble in 96% sulfuric acid and thus in solubility class N.
- As an amine with less than six carbons, ethylmethylamine is soluble in water. It is soluble in ether and its aqueous solutions turn litmus paper blue, therefore it is basic. Ethylmethylamine is in solubility class SB.
- Propoxybenzene is insoluble in water because it has more than five carbon atoms. It is a neutral compound with only carbon, hydrogen, and oxygen and is insoluble in 5% sodium hydroxide solution, and 5% hydrochloric acid solution. However, propoxybenzene is soluble in 96% sulfuric acid solution and in solubility class N.
- Propanal is soluble in water because it has less than five carbons. As a neutral compound, it is soluble in ether and its aqueous solutions do not change the color of litmus paper. Propanal is in solubility class S1.
- As an aryl halide, 1,3‐Dibromobenzene is insoluble in water, 5% sodium hydroxide solution, 5% hydrochloric acid solution, and 96% sulfuric acid. 1,3‐Dibromobenzene is in solubility class I.
- Propanoic acid is soluble in water because it contains less than five carbon atoms. It is soluble in ether, but its aqueous solutions turn litmus paper red. Propanoic acid is in solubility class SA.
- As a weak organic acid, benzenesulfonamide is insoluble in water. It is soluble in 5% sodium hydroxide solution but insoluble in 5% sodium bicarbonate solution. Benzenesulfonamide is in solubility class A2.
- 1‐Butanol is soluble in water because it contains less than five carbon atoms. It is soluble in ether and its aqueous solutions do not change the color of litmus. 1‐Butanol is in solubility class S1.
- Methyl propanoate is soluble in water since it contains less than five carbon atoms. It is soluble in ether and its aqueous solutions do not change the color of litmus. Methyl propanoate is in solubility class S1.
- 4‐Methylcyclohexanone is insoluble in water since it contains more than five carbon atoms. It is also insoluble in 5% sodium hydroxide solution and 5% hydrochloric acid solution, but soluble in 96% sulfuric acid. Therefore, 4‐methylcyclohexanone is in solubility class N.
- Since 4‐Aminobiphenyl is an aniline, it is insoluble in water. It is insoluble in 5% sodium hydroxide solution, but soluble in 5% hydrochloric acid solution. 4‐Aminobiphenyl is in solubility class B.
- Since 4‐Methylacetophenone contains more than five carbon atoms, it is insoluble in water. It is also insoluble in 5% sodium hydroxide solution and 5% hydrochloric acid solution, but soluble in 96% sulfuric acid. Therefore, 4‐methylacetophenone is in solubility class N.
- Naphthalene is insoluble in water since it contains more than five carbon atoms. It is insoluble in 5% sodium hydroxide solution and 5% hydrochloric acid solution. However, naphthalene is soluble in 96% sulfuric acid, and therefore in solubility class N.
- Phenylalanine is an amino acid, thus is amphoteric, and soluble in water. Phenylalanine is insoluble in ether and thus in solubility class S2.
- Benzoin is insoluble in water since it has more than five carbon atoms. It is insoluble in water, 5% sodium hydroxide solution, and 5% hydrochloric acid solution. However, benzoin is soluble in 96% sulfuric acid, and therefore in solubility class N.
- As a strong organic acid, 4‐hydroxybenzenesulfonic acid is insoluble in water. However, it is soluble in 5% sodium hydroxide solution and 5% sodium bicarbonate solution. 4‐Hydroxybenzenesulfonic acid is in solubility class A1.
- Listed in order from least basic to most basic (see next question).
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Benzanilide Solubility class N Pentylamine Solubility class SB Diphenylamine Solubility class N Benzylamine Solubility class SB 4‐Methylaniline Solubility class B Butanamide Solubility class S1 - Listed in order from least soluble to most soluble in water.
- Smaller alcohols are more soluble.
- More hydroxyl groups increase solubility.
- Branching increases solubility.
- N < S1–N < SB < S2
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Methanol Solubility class S1 Isopropyl alcohol Solubility class S1 Ethanol Solubility class S1 1‐Butanol Solubility class S1 -
Butane Solubility class I 1,4‐Butanediol Solubility class S2 1‐Butanol Solubility class S1 - ...
1‐Butanol Solubility class S1
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Erscheint lt. Verlag | 13.3.2023 |
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Sprache | englisch |
Themenwelt | Naturwissenschaften ► Chemie ► Organische Chemie |
Schlagworte | Analytical Chemistry • Analytische Chemie • Chemie • Chemistry • Organic Chemistry • Organische Chemie • Organische Verbindungen |
ISBN-10 | 1-119-79992-9 / 1119799929 |
ISBN-13 | 978-1-119-79992-4 / 9781119799924 |
Haben Sie eine Frage zum Produkt? |
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