Organic And Biological Chemistry
Organic And Biological Chemistry
7th Edition
ISBN: 9781305081079
Author: STOKER, H. Stephen (howard Stephen)
Publisher: Cengage Learning,
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Chapter 1, Problem 1.144EP

(a)

Interpretation Introduction

Interpretation:

The member of the given pair which is expected to have high boiling point has to be identified.

Concept Introduction:

The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane.  If the same is present in cycloalkane, then it is known as halogenated cycloalkane.  They are product of reaction between alkane/cycloalkane with halogens.

Physical properties of halogenated alkanes:

Boiling point of halogenated hydrocarbon is usually higher than the corresponding hydrocarbon.  This is because, there is a polarity difference between carbon and halogen atom.  This result in increased dipole‑dipole interactions.

General trend considering the boiling point and melting point of halogenated hydrocarbon are,

  • Melting and boiling points increase with the increase in size of alkyl groups that is present.  Due to the increasing intermolecular forces, the melting and boiling point increases.
  • As the size of halogen atom increases, the melting point and boiling point also increases.

Halogenated hydrocarbons do not possess hydrogen bonding capability.  Therefore, solubility of halogenated hydrocarbon is limited.

(b)

Interpretation Introduction

Interpretation:

The member of the given pair which is expected to have high boiling point has to be identified.

Concept Introduction:

The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane.  If the same is present in cycloalkane, then it is known as halogenated cycloalkane.  They are product of reaction between alkane/cycloalkane with halogens.

Physical properties of halogenated alkanes:

Boiling point of halogenated hydrocarbon is usually higher than the corresponding hydrocarbon.  This is because, there is a polarity difference between carbon and halogen atom.  This result in increased dipole‑dipole interactions.

General trend considering the boiling point and melting point of halogenated hydrocarbon are,

  • Melting and boiling points increase with the increase in size of alkyl groups that is present.  Due to the increasing intermolecular forces, the melting and boiling point increases.
  • As the size of halogen atom increases, the melting point and boiling point also increases.

Halogenated hydrocarbons do not possess hydrogen bonding capability.  Therefore, solubility of halogenated hydrocarbon is limited.

(c)

Interpretation Introduction

Interpretation:

The member of the given pair which is expected to have high boiling point has to be identified.

Concept Introduction:

The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane.  If the same is present in cycloalkane, then it is known as halogenated cycloalkane.  They are product of reaction between alkane/cycloalkane with halogens.

Physical properties of halogenated alkanes:

Boiling point of halogenated hydrocarbon is usually higher than the corresponding hydrocarbon.  This is because, there is a polarity difference between carbon and halogen atom.  This result in increased dipole‑dipole interactions.

General trend considering the boiling point and melting point of halogenated hydrocarbon are,

  • Melting and boiling points increase with the increase in size of alkyl groups that is present.  Due to the increasing intermolecular forces, the melting and boiling point increases.
  • As the size of halogen atom increases, the melting point and boiling point also increases.

Halogenated hydrocarbons do not possess hydrogen bonding capability.  Therefore, solubility of halogenated hydrocarbon is limited.

(d)

Interpretation Introduction

Interpretation:

The member of the given pair which is expected to have high boiling point has to be identified.

Concept Introduction:

The derivative of alkane with halogen instead of one or more hydrogen atoms is known as halogenated alkane.  If the same is present in cycloalkane, then it is known as halogenated cycloalkane.  They are product of reaction between alkane/cycloalkane with halogens.

Physical properties of halogenated alkanes:

Boiling point of halogenated hydrocarbon is usually higher than the corresponding hydrocarbon.  This is because, there is a polarity difference between carbon and halogen atom.  This result in increased dipole‑dipole interactions.

General trend considering the boiling point and melting point of halogenated hydrocarbon are,

  • Melting and boiling points increase with the increase in size of alkyl groups that is present.  Due to the increasing intermolecular forces, the melting and boiling point increases.
  • As the size of halogen atom increases, the melting point and boiling point also increases.

Halogenated hydrocarbons do not possess hydrogen bonding capability.  Therefore, solubility of halogenated hydrocarbon is limited.

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Chapter 1 Solutions

Organic And Biological Chemistry

Ch. 1.5 - Prob. 2QQCh. 1.5 - Prob. 3QQCh. 1.6 - Prob. 1QQCh. 1.6 - Prob. 2QQCh. 1.6 - Prob. 3QQCh. 1.6 - Prob. 4QQCh. 1.7 - Prob. 1QQCh. 1.7 - Prob. 2QQCh. 1.8 - Prob. 1QQCh. 1.8 - Prob. 2QQCh. 1.8 - Prob. 3QQCh. 1.8 - Prob. 4QQCh. 1.8 - Prob. 5QQCh. 1.8 - Prob. 6QQCh. 1.8 - Prob. 7QQCh. 1.9 - Prob. 1QQCh. 1.9 - Prob. 2QQCh. 1.10 - Prob. 1QQCh. 1.10 - Prob. 2QQCh. 1.11 - Prob. 1QQCh. 1.11 - Prob. 2QQCh. 1.11 - Prob. 3QQCh. 1.12 - Prob. 1QQCh. 1.12 - Prob. 2QQCh. 1.12 - Prob. 3QQCh. 1.13 - Prob. 1QQCh. 1.13 - Prob. 2QQCh. 1.13 - Prob. 3QQCh. 1.14 - Prob. 1QQCh. 1.14 - Prob. 2QQCh. 1.14 - Prob. 3QQCh. 1.15 - Prob. 1QQCh. 1.15 - Prob. 2QQCh. 1.16 - Prob. 1QQCh. 1.16 - Prob. 2QQCh. 1.16 - Prob. 3QQCh. 1.17 - Prob. 1QQCh. 1.17 - Prob. 2QQCh. 1.17 - Prob. 3QQCh. 1.17 - Prob. 4QQCh. 1.18 - Prob. 1QQCh. 1.18 - Prob. 2QQCh. 1.18 - Prob. 3QQCh. 1.18 - Prob. 4QQCh. 1 - Prob. 1.1EPCh. 1 - Prob. 1.2EPCh. 1 - Prob. 1.3EPCh. 1 - Prob. 1.4EPCh. 1 - Indicate whether each of the following situations...Ch. 1 - Indicate whether each of the following situations...Ch. 1 - Prob. 1.7EPCh. 1 - Prob. 1.8EPCh. 1 - What is the difference between a saturated...Ch. 1 - What structural feature is present in an...Ch. 1 - Prob. 1.11EPCh. 1 - Prob. 1.12EPCh. 1 - Prob. 1.13EPCh. 1 - Prob. 1.14EPCh. 1 - Prob. 1.15EPCh. 1 - Prob. 1.16EPCh. 1 - Convert the expanded structural formulas in...Ch. 1 - Prob. 1.18EPCh. 1 - Prob. 1.19EPCh. 1 - Prob. 1.20EPCh. 1 - Prob. 1.21EPCh. 1 - Prob. 1.22EPCh. 1 - Prob. 1.23EPCh. 1 - Prob. 1.24EPCh. 1 - Prob. 1.25EPCh. 1 - Prob. 1.26EPCh. 1 - Indicate whether each of the following would be...Ch. 1 - Indicate whether each of the following would be...Ch. 1 - Prob. 1.29EPCh. 1 - Explain why two different straight-chain alkanes...Ch. 1 - With the help of Table 12-1, indicate how many...Ch. 1 - Prob. 1.32EPCh. 1 - How many of the numerous eight-carbon alkane...Ch. 1 - How many of the numerous seven-carbon alkane...Ch. 1 - For each of the following pairs of structures,...Ch. 1 - For each of the following pairs of structures,...Ch. 1 - Convert each of the following linear condensed...Ch. 1 - Prob. 1.38EPCh. 1 - Prob. 1.39EPCh. 1 - Prob. 1.40EPCh. 1 - Prob. 1.41EPCh. 1 - Prob. 1.42EPCh. 1 - Prob. 1.43EPCh. 1 - Prob. 1.44EPCh. 1 - Prob. 1.45EPCh. 1 - Prob. 1.46EPCh. 1 - Prob. 1.47EPCh. 1 - Prob. 1.48EPCh. 1 - Prob. 1.49EPCh. 1 - Prob. 1.50EPCh. 1 - Prob. 1.51EPCh. 1 - Prob. 1.52EPCh. 1 - Draw a condensed structural formula for each of...Ch. 1 - Draw a condensed structural formula for each of...Ch. 1 - Prob. 1.55EPCh. 1 - For each of the alkanes in Problem 12-54,...Ch. 1 - Explain why the name given for each of the...Ch. 1 - Prob. 1.58EPCh. 1 - Indicate whether or not the two alkanes in each of...Ch. 1 - Prob. 1.60EPCh. 1 - How many of the 18 C8 alkane constitutional...Ch. 1 - How many of the nine C7 alkane constitutional...Ch. 1 - Prob. 1.63EPCh. 1 - Prob. 1.64EPCh. 1 - Prob. 1.65EPCh. 1 - Prob. 1.66EPCh. 1 - Do the line-angle structural formulas in each of...Ch. 1 - Do the line-angle structural formulas in each of...Ch. 1 - Convert each of the condensed structural formulas...Ch. 1 - Convert each of the condensed structural formulas...Ch. 1 - Assign an IUPAC name to each of the compounds in...Ch. 1 - Prob. 1.72EPCh. 1 - Prob. 1.73EPCh. 1 - Prob. 1.74EPCh. 1 - For each of the alkane structures in Problem...Ch. 1 - For each of the alkane structures in Problem...Ch. 1 - Prob. 1.77EPCh. 1 - Prob. 1.78EPCh. 1 - Prob. 1.79EPCh. 1 - Prob. 1.80EPCh. 1 - Prob. 1.81EPCh. 1 - Prob. 1.82EPCh. 1 - Draw condensed structural formulas for the...Ch. 1 - Draw condensed structural formulas for the...Ch. 1 - To which carbon atoms in a hexane molecule can...Ch. 1 - Prob. 1.86EPCh. 1 - Prob. 1.87EPCh. 1 - Prob. 1.88EPCh. 1 - Give an acceptable alternate name for each of the...Ch. 1 - Prob. 1.90EPCh. 1 - Prob. 1.91EPCh. 1 - Prob. 1.92EPCh. 1 - Prob. 1.93EPCh. 1 - Prob. 1.94EPCh. 1 - What is the molecular formula for each of the...Ch. 1 - Prob. 1.96EPCh. 1 - Prob. 1.97EPCh. 1 - Prob. 1.98EPCh. 1 - Prob. 1.99EPCh. 1 - How many secondary carbon atoms are present in...Ch. 1 - Assign an IUPAC name to each of the following...Ch. 1 - Assign an IUPAC name to each of the following...Ch. 1 - Prob. 1.103EPCh. 1 - Prob. 1.104EPCh. 1 - Prob. 1.105EPCh. 1 - Prob. 1.106EPCh. 1 - What is the molecular formula for each of the...Ch. 1 - Prob. 1.108EPCh. 1 - Prob. 1.109EPCh. 1 - Prob. 1.110EPCh. 1 - Prob. 1.111EPCh. 1 - Prob. 1.112EPCh. 1 - Determine whether cistrans isomerism is possible...Ch. 1 - Prob. 1.114EPCh. 1 - Prob. 1.115EPCh. 1 - Prob. 1.116EPCh. 1 - Prob. 1.117EPCh. 1 - Indicate whether the members of each of the...Ch. 1 - Prob. 1.119EPCh. 1 - Prob. 1.120EPCh. 1 - Prob. 1.121EPCh. 1 - Prob. 1.122EPCh. 1 - Prob. 1.123EPCh. 1 - Which member in each of the following pairs of...Ch. 1 - Prob. 1.125EPCh. 1 - Prob. 1.126EPCh. 1 - Answer the following questions about the...Ch. 1 - Prob. 1.128EPCh. 1 - Prob. 1.129EPCh. 1 - Prob. 1.130EPCh. 1 - Write molecular formulas for all the possible...Ch. 1 - Write molecular formulas for all the possible...Ch. 1 - Prob. 1.133EPCh. 1 - Prob. 1.134EPCh. 1 - Prob. 1.135EPCh. 1 - Assign an IUPAC name to each of the following...Ch. 1 - Prob. 1.137EPCh. 1 - Prob. 1.138EPCh. 1 - Prob. 1.139EPCh. 1 - Prob. 1.140EPCh. 1 - Prob. 1.141EPCh. 1 - Prob. 1.142EPCh. 1 - Prob. 1.143EPCh. 1 - Prob. 1.144EPCh. 1 - Prob. 1.145EPCh. 1 - Prob. 1.146EPCh. 1 - Give the IUPAC names for the eight isomeric...Ch. 1 - Prob. 1.148EP
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