ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG
ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG
5th Edition
ISBN: 9781260701128
Author: SMITH
Publisher: MCG
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Chapter 4, Problem 4.41P
Interpretation Introduction

(a)

Interpretation: The explanation corresponding to the incorrect IUPAC name 2,2dimethyl4ethylheptane is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing structural formula from IUPAC are:

1. First identify the word root for the given compound.

2. The suffix used in the compound like –ene.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

Expert Solution
Check Mark

Answer to Problem 4.41P

The naming of substituents attached to the longest carbon chain is not in alphabetical order. The correct IUPAC name is 4ethyl2,2dimethylheptane.

Explanation of Solution

The given IUPAC name is 2,2dimethyl4ethylheptane.

The structure corresponding to the given IUPAC name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  1

Figure 1

Rules for writing IUPAC name from structural formula are:

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

The given name is 2,2dimethyl4ethylheptane. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. In the given name, the naming of substituent is not in alphabetical order. Therefore, the correct IUPAC name is 4ethyl2,2dimethylheptane.

Conclusion

The naming of substituents attached to the longest carbon chain is not in alphabetical order. The correct IUPAC name is 4ethyl2,2dimethylheptane.

Interpretation Introduction

(b)

Interpretation: The explanation corresponding to the incorrect IUPAC name 5ethyl2methylhexane is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing structural formula from IUPAC are:

1. First identify the word root for the given compound.

2. The suffix used in the compound like –ene.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

Expert Solution
Check Mark

Answer to Problem 4.41P

The longest carbon chain in the given IUPAC name contains seven carbon atoms instead of six carbon atoms. The correct IUPAC name is 2,5dimethylheptane.

Explanation of Solution

The given IUPAC name is 5ethyl2methylhexane.

The structure corresponding to the given IUPAC name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  2

Figure 2

According to the given IUPAC name, the structure contains six carbon atoms.

Rules for writing IUPAC name from structural formula are:

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

Thus, the correct structure for the given name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  3

Figure 3

The longest carbon chain in the given IUPAC name contains seven carbon atoms instead of six carbon atoms. Thus, the correct IUPAC name is 2,5dimethylheptane.

Conclusion

The longest carbon chain in the given IUPAC name contains seven carbon atoms instead of six carbon atoms., the correct IUPAC name is 2,5dimethylheptane.

Interpretation Introduction

(c)

Interpretation: The explanation corresponding to the given incorrect IUPAC name 2methyl2isopropylheptane is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing structural formula from IUPAC are:

1. First identify the word root for the given compound.

2. The suffix used in the compound like –ene.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

Expert Solution
Check Mark

Answer to Problem 4.41P

The longest carbon chain in the given IUPAC name contains eight carbon atoms instead of seven carbon atoms. The correct IUPAC name is 2,3,3trimethyloctane.

Explanation of Solution

The given IUPAC name is 2methyl2isopropylheptane.

The structure corresponding to the given IUPAC name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  4

Figure 4

According to the given IUPAC name, the structure contains seven carbon atoms.

Rules for writing IUPAC name from structural formula are:

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

Thus, the correct structure for the given name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  5

Figure 5

The longest carbon chain in the given IUPAC name contains eight carbon atoms instead of seven carbon atoms. Therefore, the correct IUPAC name is 2,3,3trimethyloctane.

Conclusion

The longest carbon chain in the given IUPAC name contains eight carbon atoms instead of seven carbon atoms. The correct IUPAC name is 2,3,3trimethyloctane.

Interpretation Introduction

(d)

Interpretation: The explanation corresponding to the given incorrect IUPAC name 1,5dimethylcyclohexane is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing structural formula from IUPAC are:

1. First identify the word root for the given compound.

2. The suffix used in the compound like –ene.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

Expert Solution
Check Mark

Answer to Problem 4.41P

The structure corresponding to the given name is incorrect because the numbering of substituents is wrong. The correct IUPAC name is 1,3dimethylcyclohexane.

Explanation of Solution

The given IUPAC name is 1,5dimethylcyclohexane.

The structure corresponding to the given IUPAC name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  6

Figure 6

Rules for writing IUPAC name from structural formula are:

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

The given name is 1,5dimethylcyclohexane. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order.

The structure corresponding to the given name is incorrect because higher number is assigned to the second methyl substituent.

Therefore, the correct structure is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  7

Figure 7

Thus, the correct IUPAC name is 1,3dimethylcyclohexane.

Conclusion

The structure corresponding to the given name is incorrect because higher number is assigned to the second substituent. The correct IUPAC name is 1,3dimethylcyclohexane.

Interpretation Introduction

(e)

Interpretation: The explanation corresponding to the incorrect IUPAC name 1ethyl2,6dimethylcycloheptane is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing structural formula from IUPAC are:

1. First identify the word root for the given compound.

2. The suffix used in the compound like –ene.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

Expert Solution
Check Mark

Answer to Problem 4.41P

The structure corresponding to the given name is incorrect because higher number is assigned to the second substituent. The correct IUPAC name is 2ethyl1,4dimethylcycloheptane.

Explanation of Solution

The given IUPAC name is 1ethyl2,6dimethylcycloheptane.

The structure corresponding to the given IUPAC name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  8

Figure 8

Rules for writing IUPAC name from structural formula are:

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

The given name is 1ethyl2,6dimethylcycloheptane. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order.

The structure corresponding to the given name is incorrect because higher number is assigned to the second substituent.

Therefore, the correct structure is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  9

Figure 9

Thus, the correct IUPAC name is 2ethyl1,4dimethylcycloheptane.

Conclusion

The structure corresponding to the given name is incorrect because higher number is assigned to the second substituent. The correct IUPAC name is 2ethyl1,4dimethylcycloheptane.

Interpretation Introduction

(f)

Interpretation: The explanation corresponding to the incorrect IUPAC name 5,5,6trimethyloctane is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing structural formula from IUPAC are:

1. First identify the word root for the given compound.

2. The suffix used in the compound like –ene.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

Expert Solution
Check Mark

Answer to Problem 4.41P

The structure corresponding to the given name is incorrect because the numbering of substituents is wrong. The correct IUPAC name is 3,4,4trimethyloctane.

Explanation of Solution

The given IUPAC name is 5,5,6trimethyloctane.

The structure corresponding to the given IUPAC name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  10

Figure 10

Rules for writing IUPAC name from structural formula are:

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

The given name is 5,5,6trimethyloctane. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order.

The structure corresponding to the given name is incorrect because substituents should get lowest locant number.

Therefore, the correct structure is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  11

Figure 11

Thus, the correct IUPAC name is 3,4,4trimethyloctane.

Conclusion

The structure corresponding to the given name is incorrect because higher number is assigned to the second substituent. The correct IUPAC name is 3,4,4trimethyloctane.

Interpretation Introduction

(g)

Interpretation: The explanation corresponding to the incorrect IUPAC name 3butyl2,2dimethylhexane is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing structural formula from IUPAC are:

1. First identify the word root for the given compound.

2. The suffix used in the compound like –ene.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

Expert Solution
Check Mark

Answer to Problem 4.41P

The structure corresponding to the given name is incorrect because the numbering of substituents is wrong. The correct IUPAC name is 4tertbutyloctane.

Explanation of Solution

The given IUPAC name is 3butyl2,2dimethylhexane.

The structure corresponding to the given IUPAC name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  12

Figure 12

Rules for writing IUPAC name from structural formula are:

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

The given name is 3butyl2,2dimethylhexane. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order.

Therefore, the correct structure is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  13

Figure 13

Thus, the correct IUPAC name is 4tertbutyloctane.

Conclusion

The structure corresponding to the given name is incorrect because higher number is assigned to the second substituent. The correct IUPAC name is 4tertbutyloctane.

Interpretation Introduction

(h)

Interpretation: The explanation corresponding to the incorrect IUPAC name 1,3dimethylbutane is to be stated.

Concept introduction: The systematic naming of organic compound is given by IUPAC nomenclature. The naming of organic compound is done such that the structure of organic compound is correctly interpreted from the name.

Rules for writing structural formula from IUPAC are:

4. First identify the word root for the given compound.

5. The suffix used in the compound like –ene.

6. Identify the position, location, and number of the substituent bonded to the carbon chain.

Expert Solution
Check Mark

Answer to Problem 4.41P

The structure corresponding to the given name is incorrect because higher number is assigned to the second substituent. The correct IUPAC name is 2methylpentane.

Explanation of Solution

The given IUPAC name is 1,3dimethylbutane.

The structure corresponding to the given IUPAC name is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  14

Figure 14

Rules for writing IUPAC name from structural formula are:

1. First identify the longest carbon chain.

2. The next step is to identify the groups attached to the longest chain.

3. Identify the position, location, and number of the substituent bonded to the carbon chain.

4. Use prefix di, tri, tetra if same type of substituent is present.

5. Name the substituents in alphabetical order.

The given name is 1,3dimethylbutane. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order.

Therefore, the correct structure is shown below.

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG, Chapter 4, Problem 4.41P , additional homework tip  15

Figure 15

The longest carbon chain contains five carbon atoms instead of four carbon atoms.

Thus, the correct IUPAC name is 2methylpentane.

Conclusion

The structure corresponding to the given name is incorrect because higher number is assigned to the second substituent. The correct IUPAC name is 2methylpentane.

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Chapter 4 Solutions

ORG.CHEMISTRY W/ACCESS+MODEL KIT PKG

Ch. 4 - Give the IUPAC name for each compound.Ch. 4 - Give the structure corresponding to each IUPAC...Ch. 4 - Arrange the following compounds in order of...Ch. 4 - Problem 4.14 Draw the staggered and eclipsed...Ch. 4 - Prob. 4.15PCh. 4 - Prob. 4.16PCh. 4 - Problem 4.17 a. Draw the three staggered and...Ch. 4 - Problem 4.18 Rank the following conformations in...Ch. 4 - Problem 4.19 Consider rotation around the...Ch. 4 - Calculate the destabilization present in each...Ch. 4 - Problem 4.21 Classify the ring carbons as up or...Ch. 4 - Problem 4.22 Using the cyclohexane with the C’s...Ch. 4 - Draw a second chair conformation for each...Ch. 4 - Problem 4.24 Draw both conformations for and...Ch. 4 - Problem 4.25 Draw the structure for each compound...Ch. 4 - For cis-1, 3-diethylcyclobutane, draw a a...Ch. 4 - Prob. 4.27PCh. 4 - Problem 4.28 Consider . Draw structures f or the...Ch. 4 - Problem 4.29 Draw a chair conformation of...Ch. 4 - Prob. 4.30PCh. 4 - Draw the products of each combustion reaction.Ch. 4 - Explain why beeswax is insoluble in H2O, slightly...Ch. 4 - Prob. 4.33PCh. 4 - Name each alkane using the ball-and-stick model,...Ch. 4 - Consider the substituted cyclohexane shown in the...Ch. 4 - Prob. 4.36PCh. 4 - Prob. 4.37PCh. 4 - 4.38 Give the IUPAC name for each compound. a. c....Ch. 4 - 4.39 Give the structure and IUPAC name for each of...Ch. 4 - 4.40 Draw the structure corresponding to each...Ch. 4 - Prob. 4.41PCh. 4 - 4.42 Give the IUPAC name for each compound. a....Ch. 4 - Prob. 4.43PCh. 4 - Prob. 4.44PCh. 4 - 4.45 Which conformation in each pair is higher in...Ch. 4 - 4.46 Considering rotation around the bond...Ch. 4 - Prob. 4.47PCh. 4 - 4.48 (a) Using Newman projections, draw all...Ch. 4 - 4.49 Label the sites of torsional and steric...Ch. 4 - 4.50 Calculate the barrier to rotation for each...Ch. 4 - 4.51 The eclipsed conformation of is less...Ch. 4 - (a) Draw the anti and gauche conformations for...Ch. 4 - For each compound drawn below: a.Label each OH,Br...Ch. 4 - Draw the two possible chair conformations for...Ch. 4 - For each compound drawn below: a. Draw...Ch. 4 - 4.56 Convert each of the following structures into...Ch. 4 - Prob. 4.57PCh. 4 - Prob. 4.58PCh. 4 - 4.59 Classify each pair of compounds as...Ch. 4 - Classify each pair of compounds as constitutional...Ch. 4 - Prob. 4.61PCh. 4 - 4.62 Draw the three constitutional isomers having...Ch. 4 - Prob. 4.63PCh. 4 - 4.64 Draw the products of combustion of each...Ch. 4 - 4.65 Hydrocarbons like benzene are metabolized in...Ch. 4 - Prob. 4.66PCh. 4 - Prob. 4.67PCh. 4 - Cyclopropane and cyclobutane have similar strain...Ch. 4 - Prob. 4.69PCh. 4 - Haloethanes (CH3CH2X,X=Cl,Br,I) have similar...Ch. 4 - Prob. 4.71PCh. 4 - Prob. 4.72PCh. 4 - Consider the tricyclic structure B (a) Label each...Ch. 4 - Read Appendix B on naming branched alkyl...Ch. 4 - Read Appendix B on naming bicyclic compounds. Then...
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