Organic Chemistry-Package(Custom)
Organic Chemistry-Package(Custom)
4th Edition
ISBN: 9781259141089
Author: SMITH
Publisher: MCG
bartleby

Concept explainers

Question
Book Icon
Chapter 12, Problem 12.35P
Interpretation Introduction

(a)

Interpretation: The number of rings and number of pi bonds in A is to be determined. And one possible structure is to be drawn.

Concept introduction: Degree of unsaturation is used to determine the total number of rings and pi bonds present in compound by just looking at the molecular formula. It does not specify the total number of rings and total number of pi bonds individually.

Expert Solution
Check Mark

Answer to Problem 12.35P

The number of pi bonds and number of rings in A is one. The possible structure is given in Figure 1.

Explanation of Solution

For compound A:

Before hydrogenation, the molecular formula is C5H8.

The maximum number of H's possible for nC's is 2n+2.

The maximum number of H's possible for 5C's is 2(5)+2=12.

The number of H's fewer than the maximum is calculated by formula,

FewerthanmaximumH's=MaximumH'sActualH's

Substitute the values of maximum number of H's possible and actual H's in the above formula.

FewerthanmaximumH's=12H's8H's=4H's

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation=42=2

Hence, the degree of unsaturation before hydrogenation is two.

After hydrogenation, the molecular formula is C5H10.

The maximum number of H's possible for nC's is 2n+2.

The maximum number of H's possible for 5C's is 2(5)+2=12.

The number H's fewer than the maximum is calculated by formula,

MaximumH'sActualH's=FewerthanmaximumH's

Substitute the values of maximum number of H's possible and actual H's in the above formula.

FewerthanmaximumH's=12H's10H's=2H's

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation=22=1

Hence, the degree of unsaturation after hydrogenation is one.

The number of pi bonds in A is calculated by the formula,

Numberofπbonds=(DegreeofunsaturationbeforehydrogenationDegreeofunsaturationafterhydrogenation)

Substitute the values of degree of unsaturation before hydrogenation and degree of unsaturation after hydrogenation in the above formula.

Numberofπbonds=21=1

Hence, the number of pi bonds is one.

Number of rings is calculated by the formula,

Degreeofunsaturation=Numberofπbonds+Numberofrings

Substitute the values of degree of unsaturation and number of pi bonds in the above formula.

2=1+NumberofringsNumberofrings=21=1

Hence, the number of rings is one.

The possible structure for A is,

Organic Chemistry-Package(Custom), Chapter 12, Problem 12.35P , additional homework tip  1

Figure 1

Conclusion

The number of pi bonds and number of rings in A is one. The possible structure is given in Figure 1.

Interpretation Introduction

(b)

Interpretation: The number of rings and number of pi bonds in B is to be determined. And one possible structure is to be drawn.

Concept introduction: Degree of unsaturation is used to determine the total number of rings and pi bonds present in compound by just looking at the molecular formula. It does not specify the total number of rings and total number of pi bonds individually.

Expert Solution
Check Mark

Answer to Problem 12.35P

The number of pi bonds and number of rings in B is one and two respectively. The possible structure is given in Figure 2.

Explanation of Solution

For compound B:

Before hydrogenation, the molecular formula is C10H16.

The maximum number of H's possible for nC's is 2n+2.

The maximum number of H's possible for 10C's is 2(10)+2=22.

The number of H's fewer than the maximum is calculated by formula,

FewerthanmaximumH's=MaximumH'sActualH's

Substitute the values of maximum number of H's possible and actual H's in the above formula.

FewerthanmaximumH's=22H's16H's=6H's

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation=62=3

Hence, the degree of unsaturation before hydrogenation is three.

After hydrogenation, the molecular formula is C10H18.

The maximum number of H's possible for nC's is 2n+2.

The maximum number of H's possible for 10C's is 2(10)+2=22.

The number H's fewer than the maximum is calculated by formula,

MaximumH'sActualH's=FewerthanmaximumH's

Substitute the values of maximum number of H's possible and actual H's in the above formula.

FewerthanmaximumH's=22H's18H's=4H's

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation=42=2

Hence, the degree of unsaturation after hydrogenation is two.

The number of pi bonds in A is calculated by the formula,

Numberofπbonds=(DegreeofunsaturationbeforehydrogenationDegreeofunsaturationafterhydrogenation)

Substitute the values of degree of unsaturation before hydrogenation and degree of unsaturation after hydrogenation in the above formula.

Numberofπbonds=32=1

Hence, the number of pi bonds is one.

Number of rings is calculated by the formula,

Degreeofunsaturation=Numberofπbonds+Numberofrings

Substitute the values of degree of unsaturation and number of pi bonds in the above formula.

3=1+NumberofringsNumberofrings=31=2

Hence, the number of rings is two.

The possible structure for B is,

Organic Chemistry-Package(Custom), Chapter 12, Problem 12.35P , additional homework tip  2

Figure 2

Conclusion

The number of pi bonds and number of rings in B is one and two respectively. The possible structure is given in Figure 2.

Interpretation Introduction

(c)

Interpretation: The number of rings and number of pi bonds in B is to be determined. And one possible structure is to be drawn.

Concept introduction: Degree of unsaturation is used to determine the total number of rings and pi bonds present in compound by just looking at the molecular formula. It does not specify the total number of rings and total number of pi bonds individually.

Expert Solution
Check Mark

Answer to Problem 12.35P

The number of pi bonds and number of rings in C is four and one respectively. The possible structure is given in Figure 3.

Explanation of Solution

For compound C:

Before hydrogenation, the molecular formula is C8H8.

The maximum number of H's possible for nC's is 2n+2.

The maximum number of H's possible for 8C's is 2(8)+2=18.

The number of H's fewer than the maximum is calculated by formula,

FewerthanmaximumH's=MaximumH'sActualH's

Substitute the values of maximum number of H's possible and actual H's in the above formula.

FewerthanmaximumH's=18H's8H's=10H's

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation=102=5

Hence, the degree of unsaturation before hydrogenation is five.

After hydrogenation, the molecular formula is C8H16.

The maximum number of H's possible for nC's is 2n+2.

The maximum number of H's possible for 8C's is 2(8)+2=18.

The number H's fewer than the maximum is calculated by formula,

MaximumH'sActualH's=FewerthanmaximumH's

Substitute the values of maximum number of H's possible and actual H's in the above formula.

FewerthanmaximumH's=18H's16H's=2H's

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation=22=1

Hence, the degree of unsaturation after hydrogenation is one.

The number of pi bonds in A is calculated by the formula,

Numberofπbonds=(DegreeofunsaturationbeforehydrogenationDegreeofunsaturationafterhydrogenation)

Substitute the values of degree of unsaturation before hydrogenation and degree of unsaturation after hydrogenation in the above formula.

Numberofπbonds=51=4

Hence, the number of pi bonds is four.

Number of rings is calculated by the formula,

Degreeofunsaturation=Numberofπbonds+Numberofrings

Substitute the values of degree of unsaturation and number of pi bonds in the above formula.

5=4+NumberofringsNumberofrings=54=1

Hence, the number of rings is one.

The possible structure for C is,

Organic Chemistry-Package(Custom), Chapter 12, Problem 12.35P , additional homework tip  3

Figure 3

Conclusion

The number of pi bonds and number of rings in C is four and one respectively. The possible structure is given in Figure 3.

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
Differentiate between single links and multicenter links.
I need help on my practice final, if you could explain how to solve this that would be extremely helpful for my final thursday. Please dumb it down chemistry is not my strong suit. If you could offer strategies as well to make my life easier that would be beneficial
None

Chapter 12 Solutions

Organic Chemistry-Package(Custom)

Ch. 12 - Problem 12.11 (a) Draw the structure of a compound...Ch. 12 - Prob. 12.12PCh. 12 - Prob. 12.13PCh. 12 - Prob. 12.14PCh. 12 - Prob. 12.15PCh. 12 - Prob. 12.16PCh. 12 - Prob. 12.17PCh. 12 - Problem 12.18 Draw the products formed when both...Ch. 12 - Prob. 12.19PCh. 12 - Prob. 12.20PCh. 12 - Prob. 12.21PCh. 12 - Prob. 12.22PCh. 12 - Prob. 12.23PCh. 12 - Problem 12.24 Draw the organic products in each of...Ch. 12 - Prob. 12.25PCh. 12 - Prob. 12.26PCh. 12 - Problem 12.27 Draw the products of each Sharpless...Ch. 12 - Prob. 12.28PCh. 12 - 12.29 Draw the products formed when A is treated...Ch. 12 - Prob. 12.30PCh. 12 - 12.31 Devise a synthesis of the following compound...Ch. 12 - Label each reaction as oxidation, reduction, or...Ch. 12 - Prob. 12.33PCh. 12 - Prob. 12.34PCh. 12 - Prob. 12.35PCh. 12 - Prob. 12.36PCh. 12 - 12.37 Stearidonic acid (C18H28O2) is an...Ch. 12 - Draw the organic products formed when cyclopentene...Ch. 12 - Prob. 12.39PCh. 12 - Draw the organic products formed when allylic...Ch. 12 - Draw the organic products formed in each reaction...Ch. 12 - Draw the organic products formed in each reaction....Ch. 12 - Prob. 12.43PCh. 12 - Prob. 12.44PCh. 12 - Prob. 12.45PCh. 12 - What alkene is needed to synthesize each 1,2-diol...Ch. 12 - Prob. 12.47PCh. 12 - Draw the products formed after Steps 1 and 2 in...Ch. 12 - Prob. 12.49PCh. 12 - Prob. 12.50PCh. 12 - Prob. 12.51PCh. 12 - What alkyne gives each set of products after...Ch. 12 - Prob. 12.53PCh. 12 - Prob. 12.54PCh. 12 - Prob. 12.55PCh. 12 - 12.54 An unknown compound A of molecular formula ...Ch. 12 - 12.55 DHA is a fatty acid derived from fish oil...Ch. 12 - Prob. 12.58PCh. 12 - Prob. 12.59PCh. 12 - 12.58 Epoxidation of the following allylic alcohol...Ch. 12 - What allylic alcohol and DET isomer are needed to...Ch. 12 - Devise a synthesis of each hydrocarbon from...Ch. 12 - Prob. 12.63PCh. 12 - 12.62 It is sometimes necessary to isomerize a cis...Ch. 12 - Prob. 12.65PCh. 12 - Prob. 12.66PCh. 12 - Prob. 12.67PCh. 12 - Prob. 12.68PCh. 12 - Devise a synthesis of each compound from the...Ch. 12 - Devise a synthesis of each compound from acetylene...Ch. 12 - Prob. 12.71PCh. 12 - Prob. 12.72PCh. 12 - Prob. 12.73PCh. 12 - Prob. 12.74PCh. 12 - Prob. 12.75PCh. 12 - Prob. 12.76PCh. 12 - 12.72 Draw a stepwise mechanism for the following...Ch. 12 - Prob. 12.78PCh. 12 - Prob. 12.79PCh. 12 - Prob. 12.80PCh. 12 - 12.75 Sharpless epoxidation of allylic alcohol X...
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.
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning