12-27 Explain why each name is incorrect and then write a correct name. 2-Ethyl-l-propene 5-lsopropylcyclohexene 4-Methyl-4-hexene 2-sec-Butyl-l-butene 6,6-Dimethylcyclohexene 2-Ethyl-2-hexene

Question

Want to see more full solutions like this?

Answer 1

Textbook Question

Chapter 12, Problem 17P

12-27 Explain why each name is incorrect and then write a correct name.

2-Ethyl-l-propene
5-lsopropylcyclohexene
4-Methyl-4-hexene
2-sec-Butyl-l-butene
6,6-Dimethylcyclohexene
2-Ethyl-2-hexene

Expert Solution

Interpretation Introduction

(a)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 1

2-Methyl-but-1-ene.

Explanation of Solution

2-Ethyl-1-propene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 2

Error- longest chain not correctly located.

Correct name-

2-Methyl-but-1-ene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 3

Expert Solution

Interpretation Introduction

(b)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 4

4-Isopropylcyclohexene.

Explanation of Solution

5-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 5

Error- position of the substituent not correctly mentioned.

Correct name-

4-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 6

Expert Solution

Interpretation Introduction

(c)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 7

3-Methyl-2-hexene.

Explanation of Solution

4-Methyl-4-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 8

Error- position of the double bond not correctly mentioned.

Correct name-

3-Methyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 9

Expert Solution

Interpretation Introduction

(d)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 10

2-Ethyl-3-methyl -1-pentene.

Explanation of Solution

2-sec-butyl-1-butene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 11

Error- longest chain not correctly determined.

Correct name-

2-Ethyl-3-methyl -1-pentene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 12

Expert Solution

Interpretation Introduction

(e)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 13

3,3-Dimethylcyclohexene.

Explanation of Solution

6,6-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 14

Error- position of substituents not correctly determined.

Correct name-

3,3-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 15

Expert Solution

Interpretation Introduction

(f)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 16

3-Methyl-3-Heptene.

Explanation of Solution

2-Ethyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 17

Error- longest chain not correctly determined.

Correct name-

3-Methyl-3-Heptene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 18

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

Show work. Don't give Ai generated solution

In the video, we looked at the absorbance of a certain substance and how it varies depending on what wavelength of light we are looking at. Below is a similar scan of a different substance. What color BEST describes how this substance will appear? Absorbance (AU) Violet Blue Green Orange 1.2 1.0- 0.8- 0.6- 0.4- 0.2 0.0 450 500 550 600 650 700 Wavelength (nm) violet indigo blue green yellow orange red Red O Cannot tell from this information In the above graph, what causes -450 nm wavelength of light to have a higher absorbance than light with a -550 nm wavelength? Check all that are true. The distance the light travels is different The different data points are for different substances The concentration is different at different times in the experiment Epsilon (molar absortivity) is different at different wavelengths

5. a. Data were collected for Trial 1 to determine the molar mass of a nonvolatile solid solute when dissolved in cyclo- hexane. Complete the table for the analysis (See Report Sheet). Record calculated values with the correct number of significant figures. B. Freezing Point of Cyclohexane plus Calculation Zone Unknown Solute 2. Mass of cyclohexane (g) 10.14 Part C.4 3. Mass of added solute (g) 0.255 C. Calculations 1. k; for cyclohexane (°C⚫ kg/mol) 20.0 2. Freezing point change, AT, (°C) 3.04 Part C.6 3. Mass of cyclohexane in solution (kg) 4. Moles of solute, total (mol) Show calculation. 5. Mass of solute in solution, total (g) 6. Molar mass of solute (g/mol) Show calculation.

Answer 2

Textbook Question

Chapter 12, Problem 17P

12-27 Explain why each name is incorrect and then write a correct name.

2-Ethyl-l-propene
5-lsopropylcyclohexene
4-Methyl-4-hexene
2-sec-Butyl-l-butene
6,6-Dimethylcyclohexene
2-Ethyl-2-hexene

Expert Solution

Interpretation Introduction

(a)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 1

2-Methyl-but-1-ene.

Explanation of Solution

2-Ethyl-1-propene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 2

Error- longest chain not correctly located.

Correct name-

2-Methyl-but-1-ene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 3

Expert Solution

Interpretation Introduction

(b)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 4

4-Isopropylcyclohexene.

Explanation of Solution

5-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 5

Error- position of the substituent not correctly mentioned.

Correct name-

4-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 6

Expert Solution

Interpretation Introduction

(c)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 7

3-Methyl-2-hexene.

Explanation of Solution

4-Methyl-4-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 8

Error- position of the double bond not correctly mentioned.

Correct name-

3-Methyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 9

Expert Solution

Interpretation Introduction

(d)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 10

2-Ethyl-3-methyl -1-pentene.

Explanation of Solution

2-sec-butyl-1-butene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 11

Error- longest chain not correctly determined.

Correct name-

2-Ethyl-3-methyl -1-pentene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 12

Expert Solution

Interpretation Introduction

(e)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 13

3,3-Dimethylcyclohexene.

Explanation of Solution

6,6-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 14

Error- position of substituents not correctly determined.

Correct name-

3,3-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 15

Expert Solution

Interpretation Introduction

(f)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 16

3-Methyl-3-Heptene.

Explanation of Solution

2-Ethyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 17

Error- longest chain not correctly determined.

Correct name-

3-Methyl-3-Heptene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 18

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!

Answer 3

Textbook Question

Chapter 12, Problem 17P

12-27 Explain why each name is incorrect and then write a correct name.

2-Ethyl-l-propene
5-lsopropylcyclohexene
4-Methyl-4-hexene
2-sec-Butyl-l-butene
6,6-Dimethylcyclohexene
2-Ethyl-2-hexene

Expert Solution

Interpretation Introduction

(a)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 1

2-Methyl-but-1-ene.

Explanation of Solution

2-Ethyl-1-propene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 2

Error- longest chain not correctly located.

Correct name-

2-Methyl-but-1-ene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 3

Expert Solution

Interpretation Introduction

(b)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 4

4-Isopropylcyclohexene.

Explanation of Solution

5-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 5

Error- position of the substituent not correctly mentioned.

Correct name-

4-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 6

Expert Solution

Interpretation Introduction

(c)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 7

3-Methyl-2-hexene.

Explanation of Solution

4-Methyl-4-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 8

Error- position of the double bond not correctly mentioned.

Correct name-

3-Methyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 9

Expert Solution

Interpretation Introduction

(d)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 10

2-Ethyl-3-methyl -1-pentene.

Explanation of Solution

2-sec-butyl-1-butene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 11

Error- longest chain not correctly determined.

Correct name-

2-Ethyl-3-methyl -1-pentene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 12

Expert Solution

Interpretation Introduction

(e)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 13

3,3-Dimethylcyclohexene.

Explanation of Solution

6,6-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 14

Error- position of substituents not correctly determined.

Correct name-

3,3-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 15

Expert Solution

Interpretation Introduction

(f)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 16

3-Methyl-3-Heptene.

Explanation of Solution

2-Ethyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 17

Error- longest chain not correctly determined.

Correct name-

3-Methyl-3-Heptene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 18

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!

Answer 4

Textbook Question

Chapter 12, Problem 17P

12-27 Explain why each name is incorrect and then write a correct name.

2-Ethyl-l-propene
5-lsopropylcyclohexene
4-Methyl-4-hexene
2-sec-Butyl-l-butene
6,6-Dimethylcyclohexene
2-Ethyl-2-hexene

Expert Solution

Interpretation Introduction

(a)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 1

2-Methyl-but-1-ene.

Explanation of Solution

2-Ethyl-1-propene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 2

Error- longest chain not correctly located.

Correct name-

2-Methyl-but-1-ene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 3

Expert Solution

Interpretation Introduction

(b)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 4

4-Isopropylcyclohexene.

Explanation of Solution

5-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 5

Error- position of the substituent not correctly mentioned.

Correct name-

4-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 6

Expert Solution

Interpretation Introduction

(c)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 7

3-Methyl-2-hexene.

Explanation of Solution

4-Methyl-4-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 8

Error- position of the double bond not correctly mentioned.

Correct name-

3-Methyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 9

Expert Solution

Interpretation Introduction

(d)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 10

2-Ethyl-3-methyl -1-pentene.

Explanation of Solution

2-sec-butyl-1-butene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 11

Error- longest chain not correctly determined.

Correct name-

2-Ethyl-3-methyl -1-pentene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 12

Expert Solution

Interpretation Introduction

(e)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 13

3,3-Dimethylcyclohexene.

Explanation of Solution

6,6-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 14

Error- position of substituents not correctly determined.

Correct name-

3,3-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 15

Expert Solution

Interpretation Introduction

(f)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 16

3-Methyl-3-Heptene.

Explanation of Solution

2-Ethyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 17

Error- longest chain not correctly determined.

Correct name-

3-Methyl-3-Heptene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 18

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!

Answer 5

Textbook Question

Answer 6

Textbook Question

Answer 7

Expert Solution

Interpretation Introduction

(a)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 1

2-Methyl-but-1-ene.

Explanation of Solution

2-Ethyl-1-propene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 2

Error- longest chain not correctly located.

Correct name-

2-Methyl-but-1-ene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 3

Expert Solution

Interpretation Introduction

(b)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 4

4-Isopropylcyclohexene.

Explanation of Solution

5-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 5

Error- position of the substituent not correctly mentioned.

Correct name-

4-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 6

Expert Solution

Interpretation Introduction

(c)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 7

3-Methyl-2-hexene.

Explanation of Solution

4-Methyl-4-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 8

Error- position of the double bond not correctly mentioned.

Correct name-

3-Methyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 9

Expert Solution

Interpretation Introduction

(d)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 10

2-Ethyl-3-methyl -1-pentene.

Explanation of Solution

2-sec-butyl-1-butene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 11

Error- longest chain not correctly determined.

Correct name-

2-Ethyl-3-methyl -1-pentene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 12

Expert Solution

Interpretation Introduction

(e)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 13

3,3-Dimethylcyclohexene.

Explanation of Solution

6,6-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 14

Error- position of substituents not correctly determined.

Correct name-

3,3-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 15

Expert Solution

Interpretation Introduction

(f)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 16

3-Methyl-3-Heptene.

Explanation of Solution

2-Ethyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 17

Error- longest chain not correctly determined.

Correct name-

3-Methyl-3-Heptene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 18

Answer 8

Expert Solution

Interpretation Introduction

(a)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 1

2-Methyl-but-1-ene.

Explanation of Solution

2-Ethyl-1-propene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 2

Error- longest chain not correctly located.

Correct name-

2-Methyl-but-1-ene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 3

Answer 9

Expert Solution

Answer 10

Expert Solution

Answer 11

Expert Solution

Answer 12

Interpretation Introduction

(a)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer 13

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 1

2-Methyl-but-1-ene.

Answer 14

Explanation of Solution

2-Ethyl-1-propene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 2

Error- longest chain not correctly located.

Correct name-

2-Methyl-but-1-ene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 3

Answer 15

Expert Solution

Interpretation Introduction

(b)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 4

4-Isopropylcyclohexene.

Explanation of Solution

5-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 5

Error- position of the substituent not correctly mentioned.

Correct name-

4-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 6

Answer 16

Expert Solution

Answer 17

Expert Solution

Answer 18

Expert Solution

Answer 19

Interpretation Introduction

(b)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer 20

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 4

4-Isopropylcyclohexene.

Answer 21

Explanation of Solution

5-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 5

Error- position of the substituent not correctly mentioned.

Correct name-

4-Isopropylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 6

Answer 22

Expert Solution

Interpretation Introduction

(c)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 7

3-Methyl-2-hexene.

Explanation of Solution

4-Methyl-4-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 8

Error- position of the double bond not correctly mentioned.

Correct name-

3-Methyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 9

Answer 23

Expert Solution

Answer 24

Expert Solution

Answer 25

Expert Solution

Answer 26

Interpretation Introduction

(c)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer 27

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 7

3-Methyl-2-hexene.

Answer 28

Explanation of Solution

4-Methyl-4-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 8

Error- position of the double bond not correctly mentioned.

Correct name-

3-Methyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 9

Answer 29

Expert Solution

Interpretation Introduction

(d)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 10

2-Ethyl-3-methyl -1-pentene.

Explanation of Solution

2-sec-butyl-1-butene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 11

Error- longest chain not correctly determined.

Correct name-

2-Ethyl-3-methyl -1-pentene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 12

Answer 30

Expert Solution

Answer 31

Expert Solution

Answer 32

Expert Solution

Answer 33

Interpretation Introduction

(d)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer 34

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 10

2-Ethyl-3-methyl -1-pentene.

Answer 35

Explanation of Solution

2-sec-butyl-1-butene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 11

Error- longest chain not correctly determined.

Correct name-

2-Ethyl-3-methyl -1-pentene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 12

Answer 36

Expert Solution

Interpretation Introduction

(e)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 13

3,3-Dimethylcyclohexene.

Explanation of Solution

6,6-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 14

Error- position of substituents not correctly determined.

Correct name-

3,3-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 15

Answer 37

Expert Solution

Answer 38

Expert Solution

Answer 39

Expert Solution

Answer 40

Interpretation Introduction

(e)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer 41

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 13

3,3-Dimethylcyclohexene.

Answer 42

Explanation of Solution

6,6-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 14

Error- position of substituents not correctly determined.

Correct name-

3,3-Dimethylcyclohexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 15

Answer 43

Expert Solution

Interpretation Introduction

(f)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.

Answer to Problem 17P

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 16

3-Methyl-3-Heptene.

Explanation of Solution

2-Ethyl-2-hexene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 17

Error- longest chain not correctly determined.

Correct name-

3-Methyl-3-Heptene.

Introduction To General, Organic, And Biochemistry, Chapter 12, Problem 17P , additional homework tip 18

Answer 44

Expert Solution

Answer 45

Expert Solution

Answer 46

Expert Solution

Answer 47

Interpretation Introduction

(f)

Interpretation:

To identify the error in name of the given compound and write the correct IUPAC names.

Concept Introduction:

The rules to write the IUPAC names are as follows-

The longest carbon chain is identified, and the root name is given accordingly.
All the substituents attached to the root chain are determined.
The position of the substituents is so assigned that the sum of their positions comes to be the least of all possible positions.
The prefix di, tri, tetra is used if the same substituent is present two, three and four times respectively.
All the substituents in the name are written in alphabetical order.
For a cyclic hydrocarbon the prefix cyclo- is used.