General, Organic, and Biological Chemistry
General, Organic, and Biological Chemistry
7th Edition
ISBN: 9781285853918
Author: H. Stephen Stoker
Publisher: Cengage Learning
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Chapter 12, Problem 12.124EP

(a)

Interpretation Introduction

Interpretation:

The member that has higher boiling point in the given pair has to be identified.

Concept Introduction:

Organic compounds are represented shortly by the molecular formula and structural formula.  Each and every compound has its own molecular formula.  Compounds can have same molecular formula but not same structural formula.

Alkanes are linear chain saturated hydrocarbons and cycloalkanes are cyclic carbon chain saturated hydrocarbons.  They both occur naturally.

Alkanes and cycloalkanes are hydrocarbons.  They are nonpolar molecules.  Water is a polar molecule.  Therefore, alkanes and cycloalkanes do not get solubilized in water.  In other words, alkanes and cycloalkanes are insoluble in water.

Regarding density, alkanes and cycloalkanes have density lower than water.  When alkanes and cycloalkanes are mixed with water, two layers are formed which is a result of insolubility.  Alkanes and cycloalkanes are present on top of water layer which is due to lesser density.

Boiling point of alkanes and cycloalkanes increase with an increase in carbon‑chain length or the ring size.  When considering the continuous‑chain alkanes, the boiling point of alkanes increases about 30°C for every carbon atom that is added to the chain.  The continuous alkanes which contain one to four carbon atoms are gases at room temperature.  The continuous chain alkanes that contain five to seventeen carbon atoms are liquids at room temperature.  The continuous chain alkanes that contain more than eighteen carbon atoms are solids at room temperature.

When branching happens in the carbon chain, it lowers the boiling point of alkanes.  In simple words, unbranched alkanes have more boiling point than branched alkanes with the same number of carbon atoms.

Cycloalkanes have higher boiling point compared to noncyclic alkanes with the same number of carbon atoms.  This is due to the more rigid and more symmetrical structures that occur in cyclic systems.  Cyclopropane and cyclobutane are gases at room temperature.  Cyclopentane to cyclooctane are liquids at room temperature.

(b)

Interpretation Introduction

Interpretation:

The member that has higher boiling point in the given pair has to be identified.

Concept Introduction:

Organic compounds are represented shortly by the molecular formula and structural formula.  Each and every compound has its own molecular formula.  Compounds can have same molecular formula but not same structural formula.

Alkanes are linear chain saturated hydrocarbons and cycloalkanes are cyclic carbon chain saturated hydrocarbons.  They both occur naturally.

Alkanes and cycloalkanes are hydrocarbons.  They are nonpolar molecules.  Water is a polar molecule.  Therefore, alkanes and cycloalkanes do not get solubilized in water.  In other words, alkanes and cycloalkanes are insoluble in water.

Regarding density, alkanes and cycloalkanes have density lower than water.  When alkanes and cycloalkanes are mixed with water, two layers are formed which is a result of insolubility.  Alkanes and cycloalkanes are present on top of water layer which is due to lesser density.

Boiling point of alkanes and cycloalkanes increase with an increase in carbon‑chain length or the ring size.  When considering the continuous‑chain alkanes, the boiling point of alkanes increases about 30°C for every carbon atom that is added to the chain.  The continuous alkanes which contain one to four carbon atoms are gases at room temperature.  The continuous chain alkanes that contain five to seventeen carbon atoms are liquids at room temperature.  The continuous chain alkanes that contain more than eighteen carbon atoms are solids at room temperature.

When branching happens in the carbon chain, it lowers the boiling point of alkanes.  In simple words, unbranched alkanes have more boiling point than branched alkanes with the same number of carbon atoms.

Cycloalkanes have higher boiling point compared to noncyclic alkanes with the same number of carbon atoms.  This is due to the more rigid and more symmetrical structures that occur in cyclic systems.  Cyclopropane and cyclobutane are gases at room temperature.  Cyclopentane to cyclooctane are liquids at room temperature.

(c)

Interpretation Introduction

Interpretation:

The member that has higher boiling point in the given pair has to be identified.

Concept Introduction:

Organic compounds are represented shortly by the molecular formula and structural formula.  Each and every compound has its own molecular formula.  Compounds can have same molecular formula but not same structural formula.

Alkanes are linear chain saturated hydrocarbons and cycloalkanes are cyclic carbon chain saturated hydrocarbons.  They both occur naturally.

Alkanes and cycloalkanes are hydrocarbons.  They are nonpolar molecules.  Water is a polar molecule.  Therefore, alkanes and cycloalkanes do not get solubilized in water.  In other words, alkanes and cycloalkanes are insoluble in water.

Regarding density, alkanes and cycloalkanes have density lower than water.  When alkanes and cycloalkanes are mixed with water, two layers are formed which is a result of insolubility.  Alkanes and cycloalkanes are present on top of water layer which is due to lesser density.

Boiling point of alkanes and cycloalkanes increase with an increase in carbon‑chain length or the ring size.  When considering the continuous‑chain alkanes, the boiling point of alkanes increases about 30°C for every carbon atom that is added to the chain.  The continuous alkanes which contain one to four carbon atoms are gases at room temperature.  The continuous chain alkanes that contain five to seventeen carbon atoms are liquids at room temperature.  The continuous chain alkanes that contain more than eighteen carbon atoms are solids at room temperature.

When branching happens in the carbon chain, it lowers the boiling point of alkanes.  In simple words, unbranched alkanes have more boiling point than branched alkanes with the same number of carbon atoms.

Cycloalkanes have higher boiling point compared to noncyclic alkanes with the same number of carbon atoms.  This is due to the more rigid and more symmetrical structures that occur in cyclic systems.  Cyclopropane and cyclobutane are gases at room temperature.  Cyclopentane to cyclooctane are liquids at room temperature.

(d)

Interpretation Introduction

Interpretation:

The member that has higher boiling point in the given pair has to be identified.

Concept Introduction:

Organic compounds are represented shortly by the molecular formula and structural formula.  Each and every compound has its own molecular formula.  Compounds can have same molecular formula but not same structural formula.

Alkanes are linear chain saturated hydrocarbons and cycloalkanes are cyclic carbon chain saturated hydrocarbons.  They both occur naturally.

Alkanes and cycloalkanes are hydrocarbons.  They are nonpolar molecules.  Water is a polar molecule.  Therefore, alkanes and cycloalkanes do not get solubilized in water.  In other words, alkanes and cycloalkanes are insoluble in water.

Regarding density, alkanes and cycloalkanes have density lower than water.  When alkanes and cycloalkanes are mixed with water, two layers are formed which is a result of insolubility.  Alkanes and cycloalkanes are present on top of water layer which is due to lesser density.

Boiling point of alkanes and cycloalkanes increase with an increase in carbon‑chain length or the ring size.  When considering the continuous‑chain alkanes, the boiling point of alkanes increases about 30°C for every carbon atom that is added to the chain.  The continuous alkanes which contain one to four carbon atoms are gases at room temperature.  The continuous chain alkanes that contain five to seventeen carbon atoms are liquids at room temperature.  The continuous chain alkanes that contain more than eighteen carbon atoms are solids at room temperature.

When branching happens in the carbon chain, it lowers the boiling point of alkanes.  In simple words, unbranched alkanes have more boiling point than branched alkanes with the same number of carbon atoms.

Cycloalkanes have higher boiling point compared to noncyclic alkanes with the same number of carbon atoms.  This is due to the more rigid and more symmetrical structures that occur in cyclic systems.  Cyclopropane and cyclobutane are gases at room temperature.  Cyclopentane to cyclooctane are liquids at room temperature.

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Chapter 12 Solutions

General, Organic, and Biological Chemistry

Ch. 12.5 - Prob. 2QQCh. 12.5 - Prob. 3QQCh. 12.6 - Prob. 1QQCh. 12.6 - Prob. 2QQCh. 12.6 - Prob. 3QQCh. 12.6 - Prob. 4QQCh. 12.7 - Prob. 1QQCh. 12.7 - Prob. 2QQCh. 12.8 - Prob. 1QQCh. 12.8 - Prob. 2QQCh. 12.8 - Prob. 3QQCh. 12.8 - Prob. 4QQCh. 12.8 - Prob. 5QQCh. 12.8 - Prob. 6QQCh. 12.8 - Prob. 7QQCh. 12.9 - Prob. 1QQCh. 12.9 - Prob. 2QQCh. 12.10 - Prob. 1QQCh. 12.10 - Prob. 2QQCh. 12.11 - Prob. 1QQCh. 12.11 - Prob. 2QQCh. 12.11 - Prob. 3QQCh. 12.12 - Prob. 1QQCh. 12.12 - Prob. 2QQCh. 12.12 - Prob. 3QQCh. 12.13 - Prob. 1QQCh. 12.13 - Prob. 2QQCh. 12.13 - Prob. 3QQCh. 12.14 - Prob. 1QQCh. 12.14 - Prob. 2QQCh. 12.14 - Prob. 3QQCh. 12.15 - Prob. 1QQCh. 12.15 - Prob. 2QQCh. 12.16 - Prob. 1QQCh. 12.16 - Prob. 2QQCh. 12.16 - Prob. 3QQCh. 12.17 - Prob. 1QQCh. 12.17 - Prob. 2QQCh. 12.17 - Prob. 3QQCh. 12.17 - Prob. 4QQCh. 12.18 - Prob. 1QQCh. 12.18 - Prob. 2QQCh. 12.18 - Prob. 3QQCh. 12.18 - Prob. 4QQCh. 12 - Prob. 12.1EPCh. 12 - Prob. 12.2EPCh. 12 - Prob. 12.3EPCh. 12 - Prob. 12.4EPCh. 12 - Indicate whether each of the following situations...Ch. 12 - Indicate whether each of the following situations...Ch. 12 - Prob. 12.7EPCh. 12 - Prob. 12.8EPCh. 12 - What is the difference between a saturated...Ch. 12 - Prob. 12.10EPCh. 12 - Prob. 12.11EPCh. 12 - Prob. 12.12EPCh. 12 - Prob. 12.13EPCh. 12 - Prob. 12.14EPCh. 12 - Prob. 12.15EPCh. 12 - Prob. 12.16EPCh. 12 - Prob. 12.17EPCh. 12 - Prob. 12.18EPCh. 12 - Convert the expanded structural formulas in...Ch. 12 - Prob. 12.20EPCh. 12 - Prob. 12.21EPCh. 12 - Prob. 12.22EPCh. 12 - Prob. 12.23EPCh. 12 - Prob. 12.24EPCh. 12 - Prob. 12.25EPCh. 12 - Prob. 12.26EPCh. 12 - Indicate whether each of the following would be...Ch. 12 - Indicate whether each of the following would be...Ch. 12 - Prob. 12.29EPCh. 12 - Prob. 12.30EPCh. 12 - Prob. 12.31EPCh. 12 - Prob. 12.32EPCh. 12 - Prob. 12.33EPCh. 12 - How many of the numerous seven-carbon alkane...Ch. 12 - Prob. 12.35EPCh. 12 - For each of the following pairs of structures,...Ch. 12 - Prob. 12.37EPCh. 12 - Prob. 12.38EPCh. 12 - Prob. 12.39EPCh. 12 - Prob. 12.40EPCh. 12 - Prob. 12.41EPCh. 12 - What is the name of the IUPAC prefix associated...Ch. 12 - What is the IUPAC name for each of the following...Ch. 12 - What is the IUPAC name for each of the following...Ch. 12 - Prob. 12.45EPCh. 12 - What is the chemical formula for each of the...Ch. 12 - Prob. 12.47EPCh. 12 - Prob. 12.48EPCh. 12 - Prob. 12.49EPCh. 12 - Prob. 12.50EPCh. 12 - Prob. 12.51EPCh. 12 - Prob. 12.52EPCh. 12 - Draw a condensed structural formula for each of...Ch. 12 - Draw a condensed structural formula for each of...Ch. 12 - Prob. 12.55EPCh. 12 - Prob. 12.56EPCh. 12 - Explain why the name given for each of the...Ch. 12 - Prob. 12.58EPCh. 12 - Indicate whether or not the two alkanes in each of...Ch. 12 - Prob. 12.60EPCh. 12 - How many of the 18 C8 alkane constitutional...Ch. 12 - Prob. 12.62EPCh. 12 - Prob. 12.63EPCh. 12 - Prob. 12.64EPCh. 12 - Prob. 12.65EPCh. 12 - Prob. 12.66EPCh. 12 - Do the line-angle structural formulas in each of...Ch. 12 - Do the line-angle structural formulas in each of...Ch. 12 - Convert each of the condensed structural formulas...Ch. 12 - Convert each of the condensed structural formulas...Ch. 12 - Assign an IUPAC name to each of the compounds in...Ch. 12 - Prob. 12.72EPCh. 12 - Prob. 12.73EPCh. 12 - Prob. 12.74EPCh. 12 - For each of the alkane structures in Problem...Ch. 12 - Prob. 12.76EPCh. 12 - Prob. 12.77EPCh. 12 - Prob. 12.78EPCh. 12 - Prob. 12.79EPCh. 12 - Prob. 12.80EPCh. 12 - Prob. 12.81EPCh. 12 - Prob. 12.82EPCh. 12 - Draw condensed structural formulas for the...Ch. 12 - Draw condensed structural formulas for the...Ch. 12 - To which carbon atoms in a hexane molecule can...Ch. 12 - Prob. 12.86EPCh. 12 - Prob. 12.87EPCh. 12 - Prob. 12.88EPCh. 12 - Prob. 12.89EPCh. 12 - Prob. 12.90EPCh. 12 - Prob. 12.91EPCh. 12 - Prob. 12.92EPCh. 12 - Prob. 12.93EPCh. 12 - Using the general formula for a cycloalkane,...Ch. 12 - Prob. 12.95EPCh. 12 - Prob. 12.96EPCh. 12 - Prob. 12.97EPCh. 12 - Prob. 12.98EPCh. 12 - How many secondary carbon atoms are present in...Ch. 12 - Prob. 12.100EPCh. 12 - Prob. 12.101EPCh. 12 - Assign an IUPAC name to each of the following...Ch. 12 - Prob. 12.103EPCh. 12 - What is wrong with each of the following attempts...Ch. 12 - Draw line-angle structural formulas for the...Ch. 12 - Draw line-angle structural formulas for the...Ch. 12 - Prob. 12.107EPCh. 12 - Prob. 12.108EPCh. 12 - Prob. 12.109EPCh. 12 - Prob. 12.110EPCh. 12 - Determine the number of constitutional isomers...Ch. 12 - Determine the number of constitutional isomers...Ch. 12 - Prob. 12.113EPCh. 12 - Determine whether cistrans isomerism is possible...Ch. 12 - Prob. 12.115EPCh. 12 - Prob. 12.116EPCh. 12 - Prob. 12.117EPCh. 12 - Indicate whether the members of each of the...Ch. 12 - Prob. 12.119EPCh. 12 - Prob. 12.120EPCh. 12 - Prob. 12.121EPCh. 12 - Prob. 12.122EPCh. 12 - Which member in each of the following pairs of...Ch. 12 - Prob. 12.124EPCh. 12 - Prob. 12.125EPCh. 12 - Prob. 12.126EPCh. 12 - Answer the following questions about the...Ch. 12 - Prob. 12.128EPCh. 12 - Prob. 12.129EPCh. 12 - Prob. 12.130EPCh. 12 - Prob. 12.131EPCh. 12 - Prob. 12.132EPCh. 12 - Prob. 12.133EPCh. 12 - Write structural formulas for all the possible...Ch. 12 - Assign an IUPAC name to each of the following...Ch. 12 - Assign an IUPAC name to each of the following...Ch. 12 - Prob. 12.137EPCh. 12 - Prob. 12.138EPCh. 12 - Prob. 12.139EPCh. 12 - Draw structural formulas for the following...Ch. 12 - Prob. 12.141EPCh. 12 - Prob. 12.142EPCh. 12 - Prob. 12.143EPCh. 12 - Prob. 12.144EPCh. 12 - Prob. 12.145EPCh. 12 - Prob. 12.146EPCh. 12 - Prob. 12.147EPCh. 12 - Prob. 12.148EP
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