Organic Chemistry - With Access (Custom)
Organic Chemistry - With Access (Custom)
4th Edition
ISBN: 9781259147760
Author: OHIO UNIV.
Publisher: MCG
bartleby

Videos

Textbook Question
Book Icon
Chapter 10, Problem 10.40P

Give the IUPAC name for each compound.

a. CH 2 = CHCH 2 CH ( CH 3 ) CH 2 CH 3 c. Chapter 10, Problem 10.40P, Give the IUPAC name for each compound. a. CH2=CHCH2CH(CH3)CH2CH3 c. e. b.  d. f. , example  1 e.Chapter 10, Problem 10.40P, Give the IUPAC name for each compound. a. CH2=CHCH2CH(CH3)CH2CH3 c. e. b.  d. f. , example  2

b. Chapter 10, Problem 10.40P, Give the IUPAC name for each compound. a. CH2=CHCH2CH(CH3)CH2CH3 c. e. b.  d. f. , example  3 d. Chapter 10, Problem 10.40P, Give the IUPAC name for each compound. a. CH2=CHCH2CH(CH3)CH2CH3 c. e. b.  d. f. , example  4f.Chapter 10, Problem 10.40P, Give the IUPAC name for each compound. a. CH2=CHCH2CH(CH3)CH2CH3 c. e. b.  d. f. , example  5

Expert Solution
Check Mark
Interpretation Introduction

(a)

Interpretation: The IUPAC name for the given compound 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 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.

Answer to Problem 10.40P

The IUPAC name for the given compound is 4methylhex1ene.

Explanation of Solution

The given compound is CH2=CHCH2CH(CH3)CH2CH3.

The numbering of carbon atoms present in the longest carbon chain is shown below.

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  1

Figure 1

The longest carbon chain has six carbon atoms. The root word used for six carbon atoms is hex and the suffix used for C=C linkage is –ene. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. One methyl substituents is attached to the fourth carbon atom The double bond is present between first and second carbon atom. Thus, the IUPAC name of the given structure is 4methylhex1ene.

Conclusion

The IUPAC name for the given compound is 4methylhex1ene.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The IUPAC name for the given compound 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 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.

Answer to Problem 10.40P

The IUPAC name for the given compound is 5ethyl2methyloct2ene.

Explanation of Solution

The given compound is,

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  2

Figure 2

The numbering of carbon atoms present in longest chain of the given compound is shown below.

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  3

Figure 3

The longest carbon-carbon chain has eight carbon atoms. The root word used for eight carbon atoms is oct and the suffix used for C=C linkage is –ene. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. One methyl substituent is attached to the second carbon atom and one ethyl substituent is attached to the fifth carbon atom. The double bond is present between second and third carbon atom. Thus, the IUPAC name of the given structure is 5ethyl2methyloct2ene.

Conclusion

The IUPAC name for the given compound is 5ethyl2methyloct2ene.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation: The IUPAC name for the given compound 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 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.

Answer to Problem 10.40P

The IUPAC name for the given compound is 2isopropyl4methylpent1ene.

Explanation of Solution

The given compound is,

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  4

Figure 4

The numbering of carbon atoms present in longest chain of the given compound is shown below.

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  5

Figure 5

The longest carbon-carbon chain has five carbon atoms. The root word used for five carbon atoms is pent and the suffix used for C=C linkage is –ene. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. One isopropyl substituent is attached to the second carbon atom and one methyl substituent is attached to the fourth carbon atom. The double bond is present between first and second carbon atom. Thus, the IUPAC name of the given structure is 2isopropyl4methylpent1ene.

Conclusion

The IUPAC name for the given compound is 2isopropyl4methylpent1ene.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation: The IUPAC name for the given compound is to be stated.

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

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.

Answer to Problem 10.40P

The IUPAC name for the given compound is 1ethyl5isopropylcyclohex1ene.

Explanation of Solution

The given compound is,

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  6

Figure 6

The numbering of carbon atoms present in longest carbon chain of the given compound is shown below.

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  7

Figure 7

The longest carbon chain has six carbon atoms. The root word used for six carbon atoms is hex and the suffix used for C=C linkage is –ene. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. One ethyl substituents is attached to the first carbon atom and one isopropyl substituent is attached to the fifth carbon atom. The double bond is present between first and second carbon atom. Thus, the IUPAC name of the given structure is 1ethyl5isopropylcyclohex1ene.

Conclusion

The IUPAC name for the given compound is 1ethyl5isopropylcyclohex1ene.

Expert Solution
Check Mark
Interpretation Introduction

(e)

Interpretation: The IUPAC name for the given compound 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 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.

Answer to Problem 10.40P

The IUPAC name for the given compound is 4isopropylhept4ene3ol

Explanation of Solution

The given compound is,

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  8

Figure 8

The numbering of carbon atoms present in longest carbon chain of the given compound is shown below.

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  9

Figure 9

The longest carbon chain has seven carbon atoms. The root word used for seven carbon atoms is hept and the suffix used for C=C linkage is –ene. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. One isopropyl substituents is attached to the fourth carbon atom. The double bond is present between fourth and fifth carbon atom. Another functional group present in the given structure is alcohol (OH). The suffix used for alcohol is –ol. Thus, the IUPAC name of the given structure is 4isopropylhept4ene3ol.

Conclusion

The IUPAC name for the given compound is 4isopropylhept4ene3ol.

Expert Solution
Check Mark
Interpretation Introduction

(f)

Interpretation: The IUPAC name for the given compound is to be stated.

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

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.

Answer to Problem 10.40P

The IUPAC name for the given compound is 5(secbutyl)cyclohex-2-ene1ol.

Explanation of Solution

The given compound is,

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  10

Figure 10

The numbering of carbon atoms present in longest carbon chain of the given compound is shown below.

Organic Chemistry - With Access (Custom), Chapter 10, Problem 10.40P , additional homework tip  11

Figure 11

The longest carbon chain has six carbon atoms. The root word used for six carbon atoms is hex and the suffix used for C=C linkage is –ene. The hydrocarbons that are attached to the longest chain are called substituents and they are written as prefix in alphabetical order. One secondary butyl substituent is attached to the fifth carbon atom. The double bond is present between first and second carbon atom. Another functional group present in the given structure is alcohol (OH). The suffix used for alcohol is –ol. Thus, the IUPAC name of the given structure is 5(secbutyl)cyclohex-2-ene1ol.

Conclusion

The IUPAC name of the given structure is 5(secbutyl)cyclohex-2-ene1ol.

Want to see more full solutions like this?

Subscribe now to access step-by-step solutions to millions of textbook problems written by subject matter experts!
Students have asked these similar questions
ALCOHOLS 1. WHY IS ETHANOL MORE SOLUBLE IN WATER THAN 1-HEXANOL? 2. WHAT IS DENATURED ALCOHOL? AND WHY IS ALCOHOL DENATURED?   ETHER 1. WHY DOES DIETHYL ETHER HAVE MUCH LOWER BOILING POINT THAN 1-BUTANOL?
What alkenes are formed when attached alcohol is dehydrated with TsOH?Label the major product when a mixture results
Give the IUPAC name for each alkene.

Chapter 10 Solutions

Organic Chemistry - With Access (Custom)

Ch. 10 - Linolenic acidTable 10.2 and stearidonic acid are...Ch. 10 - Prob. 10.12PCh. 10 - Prob. 10.13PCh. 10 - Prob. 10.14PCh. 10 - Prob. 10.15PCh. 10 - Prob. 10.16PCh. 10 - Prob. 10.17PCh. 10 - Prob. 10.18PCh. 10 - Prob. 10.19PCh. 10 - Which compounds A-D in Figure 10.12 are formed by...Ch. 10 - What two alkenes give rise to each alcohol as the...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 - Prob. 10.26PCh. 10 - Borane is sold for laboratory use as a complex...Ch. 10 - What alkylborane is formed from hydroboration of...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. 10.31PCh. 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. 10.36PCh. 10 - Calculate the number of degrees of unsaturation f...Ch. 10 - Prob. 10.38PCh. 10 - The fertility drug clomiphene trade name Clomid is...Ch. 10 - Give the IUPAC name for each compound. a....Ch. 10 - Give the structure corresponding to each name. a....Ch. 10 - 10.40 (a) Draw all possible stereoisomers of, and...Ch. 10 - Prob. 10.43PCh. 10 - 10.42 Now that you have learned how to name...Ch. 10 - Prob. 10.45PCh. 10 - Prob. 10.46PCh. 10 - Prob. 10.47PCh. 10 - Prob. 10.48PCh. 10 - By using the bond dissociation energies in...Ch. 10 - Prob. 10.50PCh. 10 - Repeat Problem 10.50 with CH32C=CH2 as the...Ch. 10 - What alkene can be used to prepare each alkyl...Ch. 10 - Prob. 10.53PCh. 10 - Draw the constitutional isomer formed in each...Ch. 10 - Prob. 10.55PCh. 10 - Draw all stereoisomers formed in each reaction....Ch. 10 - Prob. 10.57PCh. 10 - Prob. 10.58PCh. 10 - Prob. 10.59PCh. 10 - Draw a stepwise mechanism for the following...Ch. 10 - Draw a stepwise mechanism for each reaction. a.b.Ch. 10 - Draw a stepwise mechanism that shows how all three...Ch. 10 - Less stable alkenes can be isomerized to more...Ch. 10 - Prob. 10.64PCh. 10 - Prob. 10.65PCh. 10 - Bromoetherification, the addition of the elements...Ch. 10 - Devise a synthesis of each product from the given...Ch. 10 - Prob. 10.68PCh. 10 - Prob. 10.69PCh. 10 - Prob. 10.70PCh. 10 - 10.66 Explain why A is a stable compound but B is...Ch. 10 - Prob. 10.72PCh. 10 - Prob. 10.73PCh. 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...
Knowledge Booster
Background pattern image
Chemistry
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
Text book image
Chemistry: Principles and Practice
Chemistry
ISBN:9780534420123
Author:Daniel L. Reger, Scott R. Goode, David W. Ball, Edward Mercer
Publisher:Cengage Learning
07 Physical Properties of Organic Compounds; Author: Mindset;https://www.youtube.com/watch?v=UjlSgwq4w6U;License: Standard YouTube License, CC-BY