General, Organic, & Biological Chemistry
General, Organic, & Biological Chemistry
2nd Edition
ISBN: 9780073402789
Author: Janice Gorzynski Smith
Publisher: McGraw-Hill Education
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Chapter 10, Problem 10.36UKC

Answer the questions in Problem 10.35 for the alkane drawn below.

Chapter 10, Problem 10.36UKC, Answer the questions in Problem 10.35 for the alkane drawn below. Answer the following questions , example  1

Answer the following questions about the alkane drawn below.

Chapter 10, Problem 10.36UKC, Answer the questions in Problem 10.35 for the alkane drawn below. Answer the following questions , example  2

  1. a. Give the IUPAC name.
  2. b. Draw one constitutional isomer.
  3. c. Predict the solubility in water.
  4. d. Predict the solubility in an organic solvent.
  5. e. Write a balanced equation for complete combustion.

a.

Expert Solution
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Interpretation Introduction

Interpretation:

The IUPAC name of given compound has to be identified.

General, Organic, & Biological Chemistry, Chapter 10, Problem 10.36UKC , additional homework tip  1

Concept Introduction:

IUPAC Nomenclature:

The IUPAC Nomenclature is a systematic writing name for organic compounds.  The full form of IUPAC is known as International Union of Pure and Applied Chemistry.

There are some rules followed for writing IUPAC Nomenclature for alkane compound is given below,

  • The longest chain in the compound is known as parent name which represent the number of carbon atom present in the continuous carbon chain.  The root name for alkane compound is –ane.  The single bonds are formed in alkane compounds.
  • The suffix group denotes the functional group present in a molecule. The prefix group indicates the identity, location and number of substituents attached to the carbon compound.
  • Then name and number the substituents present in compounds.  Then use prefix di-to represent two groups, tri- refers to three groups and so on.
  • Then numbers has to be separated by using commas and the letters from numbers has to be separated by using dashes.

Explanation of Solution

In this compound, the longest continuous chain has seven carbon atoms; so the parent name can be given as hept- and add suffix name –ane for alkane molecule.  The parent name of given compound is heptane.  Then number the substituents in alphabetical order.  The ethyl group (CH2CH3) is present at third and fourth carbon.  The methyl groups (CH3) are present at third carbon position in chain.  Then add the prefix name di- to indicate two ethyl substituents (CH2CH3) present in the compound.  Hence the given compound can be named as 3,4-diethyl-3-methylheptane.

The IUPAC name of compound is given below,

General, Organic, & Biological Chemistry, Chapter 10, Problem 10.36UKC , additional homework tip  2

b.

Expert Solution
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Interpretation Introduction

Interpretation

The constitutional isomer of 3, 4-diethyl-3-methylheptane has to be explained.

General, Organic, & Biological Chemistry, Chapter 10, Problem 10.36UKC , additional homework tip  3

Concept Introduction:

Isomers:

Isomers contain two or more compounds in which the molecular formula of compounds is same but the atoms are arranged in different order. The arrangement of atoms will be in different manner.

Constitutional isomer:

The compounds have the same molecular formula but atoms are arranged in different connectivity is known as constitutional isomer.

Explanation of Solution

The isomer 3,4-diethyl-3-methylheptane has seven carbon atoms present in the longest chain. The two substituents ethyl groups (C2H5)2 are attached to chain at different positions.  The methyl groups (CH3) are attached to third carbon in chain.  The ethyl group (C2H5)2 is attached to third and fifth carbon position in chain.  The constitutional isomers have same molecular formula but the atoms are arranged in different positions.  The molecular formula is given as C12H26.  The compounds have same molecular formula but the position of substituents methyl group (CH3) is different. The possible position of substituent ethyl groups (C2H5)2 group in third and fifth carbon.  Hence the isomer can be named as 3, 5-diethyl-3-methylheptane.

The constitutional isomers of 3,4-diethyl-3-methylheptane is given below,

General, Organic, & Biological Chemistry, Chapter 10, Problem 10.36UKC , additional homework tip  4

c.

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Interpretation Introduction

Interpretation:

The solubility of given compound in water has to be predicted.

General, Organic, & Biological Chemistry, Chapter 10, Problem 10.36UKC , additional homework tip  5

Concept Introduction:

Solubility:

The solubility is defined as the solid or liquid or gaseous substance which dissolves in suitable solvent.  The nonpolar molecule has no separate positive and negative charge.  Polar molecules have separate positive and negative charges.

Explanation of Solution

The compound 3,4-diethyl-3-methylheptane is insoluble in water.  The water molecule is said to be polar molecules.  It has both positive and negative charge.  The given compound is a nonpolar alkane.  The nonpolar alkanes cannot soluble in water molecule.  Hence the given compound 3,4-diethyl-3-methylheptane is insoluble in water.

d.

Expert Solution
Check Mark
Interpretation Introduction

Interpretation:

The solubility of given compound in organic compound has to be predicted.

General, Organic, & Biological Chemistry, Chapter 10, Problem 10.36UKC , additional homework tip  6

Concept Introduction:

Solubility:

The solubility is defined as the solid or liquid or gaseous substance which dissolves in suitable solvent.  The nonpolar molecule has no separate positive and negative charge.  The Polar molecules have separate positive and negative charges.

Explanation of Solution

The given compound 3,4-diethyl-3-methylheptane is soluble in organic solvent. The reason for the solubility of the given compound, it belongs to nonpolar molecule.  Nonpolar molecules cannot soluble in polar molecule.  The nonpolar molecule has no separate charges.  Hence given molecule 3,4-diethyl-3-methylheptane is soluble in organic solvent.

e.

Expert Solution
Check Mark
Interpretation Introduction

Interpretation:

The balanced equation for complete combustion of given compound has to be written.

General, Organic, & Biological Chemistry, Chapter 10, Problem 10.36UKC , additional homework tip  7

Concept Introduction:

Combustion reaction:

The hydrocarbon compound reacts with oxygen to form carbon dioxide and water as product is known as hydrocarbon combustion reaction.  It is an exothermic reaction.  The hydrocarbon compounds are generally organic compounds contain carbon and hydrogen element.  The compounds such as alkanes, alkenes, alkynes and aromatic compounds.

The general equation is given as,

  CxHy+N(O2)x(CO2)+y2(H2O)

Where,

  • x represents the number of carbon atoms present in the hydrocarbon
  • y represents the number of carbon atoms present in the hydrocarbon
  • N represents the number of oxygen atoms requires in the hydrocarbon combustion reaction

Chemical equation:

In chemical equation, the substance reacts (reactant) to give products.  The number of atoms present in reactant side should be equal to the number of atom present in the product side.

Explanation of Solution

The compound 3,4-diethyl-3-methylheptane (C12H26) undergoes combustion in presence of flame and oxygen molecule and the product formed will be carbon di oxide and water, heat energy.

The chemical reaction for complete combustion of ethane is given below,

  2C12H26+37O2CO2+ H2O+Energy

In reactant side, it has twenty four carbon atoms and fifty two hydrogen and seventy four atoms oxygen atoms is present.  In product side there are twenty four carbon atoms and forty eight oxygen atoms present in carbon dioxide.  The fifty six hydrogen atoms and twenty six oxygen atoms are present in water molecule.  In this reaction the molecule (C12H26) reacts with sufficient oxygen to forms carbon dioxide (CO2) and water as product.

The balanced equation for complete combustion reaction of 3-ethyl-4,4-dimethylheptane is given below,

  2C12H26+37O224CO2+26H2O+Energy

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Chapter 10 Solutions

General, Organic, & Biological Chemistry

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