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Chapter 10, Problem 10.39P
Interpretation Introduction

(a)

Interpretation: The structure corresponding to the given (E)4ethylhept3ene is to be drawn.

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.

The use of prefix E and Z depends upon the location of the higher priority groups. When two higher priority groups are present on the opposite side then it is an E isomer, whereas when two higher priority groups are present on the same side then it is a Z isomer. The priority order depends upon the atomic number of the elements.

Expert Solution
Check Mark

Answer to Problem 10.39P

The structure corresponding to (E)4ethylhept3ene is shown in Figure 1.

Explanation of Solution

The given IUPAC name is (E)4ethylhept3ene.

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.

The use of prefix E and Z depends upon the location of the higher priority groups. When two higher priority groups are present on the opposite side then it is an E isomer, whereas when two higher priority groups are present on the same side then it is a Z isomer.

The given name is (E)4ethylhept3ene. The word root used in this is hept. It means structure contains seven carbon atoms. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. Therefore, the name suggests that one ethyl substituents is attached to the fourth carbon atom. The double bond is present between third and fourth carbon atom. In the given IPUAC name, the prefix used is E.

Thus, the correct structure of (E)4ethylhept3ene is shown below.

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card, Chapter 10, Problem 10.39P , additional homework tip  1

Figure 1

Conclusion

The structure corresponding to (E)4ethylhept3ene is rightfully stated.

Interpretation Introduction

(b)

Interpretation: The structure corresponding to the given 3,3dimethylcyclopentene is to be drawn.

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 10.39P

The structure corresponding to 3,3dimethylcyclopentene is shown in Figure 2.

Explanation of Solution

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.

The given name is 3,3dimethylcyclopentene. The word root used in this is pent. It means structure contains five carbon atoms in a cyclic ring. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. Therefore, the name suggests that two methyl substituents are attached to the third carbon atom. The double bond is present between first and sedcond carbon atom.

Thus, the correct structure of 3,3dimethylcyclopentene is shown below.

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card, Chapter 10, Problem 10.39P , additional homework tip  2

Figure 2

Conclusion

The structure corresponding to 3,3dimethylcyclopentene is rightfully stated.

Interpretation Introduction

(c)

Interpretation: The structure corresponding to 4vinylcyclopentene is to be drawn.

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 10.39P

The structure corresponding to 4vinylcyclopentene is shown in Figure 3.

Explanation of Solution

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.

The given name is 4vinylcyclopentene. The word root used in this is pent. It means structure contains five carbon atoms in a cyclic ring. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. Therefore, the name suggests that one vinyl substituents is attached to the fourth carbon atom. The double bond is present between first and second carbon atom.

Thus, the correct structure of 4vinylcyclopentene is shown below.

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card, Chapter 10, Problem 10.39P , additional homework tip  3

Figure 3

Conclusion

The structure corresponding to 4vinylcyclopentene is rightfully stated.

Interpretation Introduction

(d)

Interpretation: The structure corresponding to (Z)3isopropylhept2ene is to be drawn.

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.

The use of prefix E and Z depends upon the location of the higher priority groups. When two higher priority groups are present on the opposite side then it is an E isomer, whereas when two higher priority groups are present on the same side then it is a Z isomer. The priority order depends upon the atomic number of the elements.

Expert Solution
Check Mark

Answer to Problem 10.39P

The structure corresponding to (Z)3isopropylhept2ene is shown in Figure 4.

Explanation of Solution

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.

The use of prefix E and Z depends upon the location of the higher priority groups. When two higher priority groups are present on the opposite side then it is an E isomer, whereas when two higher priority groups are present on the same side then it is a Z isomer. The priority order depends upon the atomic number of the elements.

The given name is (Z)3isopropylhept2ene. The word root used in this is hept. It means structure contains seven carbon atoms. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. Therefore, the name suggests that one isopropyl substituent is attached to the third carbon atom. The double bond is present between second and third carbon atom. In the given IPUAC name, the prefix used is Z.

Thus, the correct structure of (Z)3isopropylhept2ene is shown below.

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card, Chapter 10, Problem 10.39P , additional homework tip  4

Figure 4

Conclusion

The structure corresponding to (Z)3isopropylhept2ene is rightfully stated.

Interpretation Introduction

(e)

Interpretation: The structure corresponding to cis3,4dimethylcyclopentene is to be drawn.

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 10.39P

The structure corresponding to cis3,4dimethylcyclopentene is shown in Figure 5.

Explanation of Solution

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.

The given name is cis3,4dimethylcyclopentene. The word root used in this is pent. It means structure contains five carbon atoms in a cyclic ring. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. Therefore, the name suggests that one methyl substituents is attached to the third and fourth carbon atom. The double bond is present between first and second carbon atom. The prefix cis indicates that the two methyl groups are present on same side. They can be represented either in wedge or dashed bonds.

Thus, the two correct structure of cis3,4dimethylcyclopentene is shown below.

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card, Chapter 10, Problem 10.39P , additional homework tip  5

Figure 5

Conclusion

The structure corresponding to cis3,4dimethylcyclopentene is rightfully stated.

Interpretation Introduction

(f)

Interpretation: The structure corresponding to 1isopropyl4propylcyclohexene is to be drawn.

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 10.39P

The structure corresponding to 1isopropyl4propylcyclohexene is shown in Figure 6.

Explanation of Solution

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.

The given name is 1isopropyl4propylcyclohexene. The word root used in this is hex. It means structure contains six carbon atoms in a cyclic ring. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. Therefore, the name suggests that one isopropyl substituents is attached to the first carbon atom and one propyl substituents is attached to the fourth carbon atom The double bond is present between first and second carbon atom.

Thus, the correct structure of 1isopropyl4propylcyclohexene is shown below.

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card, Chapter 10, Problem 10.39P , additional homework tip  6

Figure 6

Conclusion

The structure corresponding to 1isopropyl4propylcyclohexene is rightfully stated.

Interpretation Introduction

(g)

Interpretation: The structure corresponding to 3,4dimethylcyclohex2enol is to be drawn.

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 10.39P

The structure corresponding to 3,4dimethylcyclohex2enol is shown in Figure 7.

Explanation of Solution

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.

The given name is 3,4dimethylcyclohex2enol. The word root used in this is hex. It means structure contains hex carbon atoms in a cyclic ring. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. Therefore, the name suggests that one methyl substituents is attached to the third and fourth carbon atom. The double bond is present between second and third carbon atom. Another functional group present in the given name is alcohol (OH).

Thus, the correct structure of 3,4dimethylcyclohex2enol is shown below.

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card, Chapter 10, Problem 10.39P , additional homework tip  7

Figure 7

Conclusion

The structure corresponding to 3,4dimethylcyclohex2enol is rightfully stated.

Interpretation Introduction

(h)

Interpretation: The structure corresponding to 3,5diethylcyclohex5en3ol is to be drawn.

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 10.39P

The structure corresponding to 3,5diethylhex5en3ol is shown in Figure 8.

Explanation of Solution

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.

The given name is 3,5diethylhex5en3ol. The word root used in this is hex. It means structure contains six carbon atoms in a cyclic ring. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. Therefore, the name suggests that one ethyl substituents is attached to the third and fifth carbon atom. The double bond is present between fifth and sixth carbon atom. Another functional group present in the given name is alcohol (OH).

Thus, the correct structure of 3,5diethylhex5en3ol is shown below.

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card, Chapter 10, Problem 10.39P , additional homework tip  8

Figure 8

Conclusion

The structure corresponding to 3,5diethylhex5en3ol is rightfully stated.

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Chapter 10 Solutions

Package: Loose Leaf for Organic Chemistry with Biological Topics with Connect Access Card

Ch. 10 - Linolenic acidTable 10.2 and stearidonic acid are...Ch. 10 - Prob. 10.12PCh. 10 - Problem 10.13 What product is formed when each...Ch. 10 - Prob. 10.14PCh. 10 - Problem 10.15 Draw the products formed when each...Ch. 10 - Prob. 10.16PCh. 10 - Prob. 10.17PCh. 10 - Addition of HBr to which of the following alkenes...Ch. 10 - Problem 10.19 Draw the products, including...Ch. 10 - Prob. 10.20PCh. 10 - Problem 10.21 What two alkenes give rise to each...Ch. 10 - Prob. 10.22PCh. 10 - Problem 10.23 Draw the products of each reaction,...Ch. 10 - Problem 10.24 Draw all stereoisomers formed in...Ch. 10 - Prob. 10.25PCh. 10 - Problem 10.26 What alkylborane is formed from...Ch. 10 - Draw the products formed when each alkene is...Ch. 10 - What alkene can be used to prepare each alcohol as...Ch. 10 - Prob. 10.29PCh. 10 - Draw the products of each reaction using the two...Ch. 10 - Problem 10.31 Devise a synthesis of each compound...Ch. 10 - Give the IUPAC name for each compound. a.b.Ch. 10 - a Label the carbon-carbon double bond in A as E or...Ch. 10 - Prob. 10.34PCh. 10 - 10.35 Calculate the number of degrees of...Ch. 10 - Prob. 10.36PCh. 10 - Label the alkene in each drug as E or Z....Ch. 10 - Give the IUPAC name for each compound. a. c. e. b....Ch. 10 - Prob. 10.39PCh. 10 - 10.40 (a) Draw all possible stereoisomers of, and...Ch. 10 - Prob. 10.41PCh. 10 - 10.42 Now that you have learned how to name...Ch. 10 - Prob. 10.43PCh. 10 - Prob. 10.44PCh. 10 - Prob. 10.45PCh. 10 - Draw the products formed when (CH3)2C=CH2 is...Ch. 10 - What alkene can be used to prepare each alkyl...Ch. 10 - Prob. 10.48PCh. 10 - Draw the constitutional isomer formed in each...Ch. 10 - Prob. 10.50PCh. 10 - Draw all stereoisomers formed in each reaction. a....Ch. 10 - Draw the products of each reaction, including...Ch. 10 - Prob. 10.53PCh. 10 - Prob. 10.54PCh. 10 - Prob. 10.55PCh. 10 - 10.56 Draw a stepwise mechanism for the following...Ch. 10 - Prob. 10.57PCh. 10 - Draw a stepwise mechanism for the conversion of...Ch. 10 - Draw a stepwise mechanism that shows how all three...Ch. 10 - Less stable alkenes can be isomerized to more...Ch. 10 - Prob. 10.61PCh. 10 - Prob. 10.62PCh. 10 - Bromoetherification, the addition of the elements...Ch. 10 - Devise a synthesis of each product from the given...Ch. 10 - 10.65 Draw a synthesis of each compound from...Ch. 10 - 10.66 Explain why A is a stable compound but B is...Ch. 10 - Prob. 10.67PCh. 10 - Prob. 10.68PCh. 10 - 10.69 Lactones, cyclic esters such as compound A,...Ch. 10 - 10.70 Draw a stepwise mechanism for the following...Ch. 10 - 10.71 Like other electrophiles, carbocations add...Ch. 10 - 10.72 Draw a stepwise mechanism for the...
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