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Chapter 12, Problem 12.7P
Compound Molecular formula before hydrogenation Molecular formula after hydrogenation Number of rings Number of pi bonds
A C 10 H 12 C 10 H 16 ? ?
B ? C 4 H 10 0 1
C C 6 H 8 ? 1 ?

Complete the missing information for compounds A, B, and C, each subjected to hydrogenation.

The number of rings and π bonds refers to the reactant (A, B, or C) prior to hydrogenation.

Expert Solution & Answer
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Interpretation Introduction

Interpretation: The missing information in the given table is to be completed.

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.

Answer to Problem 12.7P

The missing information about compounds A, B and C is completed in the table given below.

Compound Molecular formula before hydrogenation Molecular formula after hydrogenation Number of rings Number of pi bonds
A C10H12 C10H16 2 3
B C4H8 C4H10 0 1
C C6H8 C6H12 1 2

Explanation of Solution

For compound A:

Before hydrogenation, the molecular formula is C10H12.

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's12H'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 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 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's16H's=6H's

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation=62=3

Hence, the degree of unsaturation after hydrogenation is three.

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=53=2

Hence, the number of pi bonds is two.

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=2+NumberofringsNumberofrings=52=3

Hence, the number of rings is three.

For compound B:

After hydrogenation, the molecular formula is C4H10.

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

The maximum number of H's possible for 4C's is 2(4)+2=10.

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

FewerthanmaximumH's=MaximumH'sActualH's

Since both maximum number of H's possible and actual H's are same. The number of H's fewer than the maximum is zero.

Hence, the degree of unsaturation after hydrogenation is zero.

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

Numberofπbonds=(DegreeofunsaturationbeforehydrogenationDegreeofunsaturationafterhydrogenation)

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

Degreeofunsaturationbefore hydrogenation=0+1=1

Hence, degree of unsaturation before hydrogenation is one.

Before hydrogenation,

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

The maximum number of H's possible for 4C's is 2(4)+2=10.

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation1=H'sfewerthanthemaximum2H'sfewerthanthemaximum=2

Hence, the number of H's fewer than the maximum is two.

The number 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 H's fewer than the maximum in the above formula.

ActualH's=10H's2H's=8H's

Hence, the molecular formula before hydrogenation is C4H8.

For compound C:

Before hydrogenation, the molecular formula is C6H8

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(6)+2=14.

The number 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=14H's8H'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.

Number of rings is calculated by the formula,

Degreeofunsaturation=Numberofπbonds+Numberofrings

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

Numberofπbonds=31=2

Hence, the number of pi bonds is two.

The degree of unsaturation after hydrogenation is equal to the number of rings present in the compound. Hence, degree of unsaturation after hydrogenation is one.

After hydrogenation,

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(6)+2=14.

The degree of unsaturation is calculated by the formula,

Degreeofunsaturation=H'sfewerthanthemaximum2H'sremovedforeachdegreeofsaturation1=H'sfewerthanthemaximum2H'sfewerthanthemaximum=2

Hence, the number of H's fewer than the maximum is two.

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 H's fewer than the maximum in the above formula.

ActualH's=14H's2H's=12H's

Hence, the molecular formula before hydrogenation is C6H12.

The missing information about compounds A, B and C is completed in the table given below.

Compound Molecular formula before hydrogenation Molecular formula after hydrogenation Number of rings Number of pi bonds
A C10H12 C10H16 2 3
B C4H8 C4H10 0 1
C C6H8 C6H12 1 2

Table 1

Conclusion

The missing information about compounds A, B and C is completed in the table 1.

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Chapter 12 Solutions

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

Ch. 12 - Problem 12.11 (a) Draw the structure of a compound...Ch. 12 - Prob. 12.12PCh. 12 - Prob. 12.13PCh. 12 - Problem 12.14 Draw the products of each...Ch. 12 - Prob. 12.15PCh. 12 - Problem 12.16 Draw all stereoisomers formed when...Ch. 12 - Prob. 12.17PCh. 12 - Problem 12.18 Draw the products formed when both...Ch. 12 - Problem 12.19 Draw the products formed when each...Ch. 12 - Prob. 12.20PCh. 12 - Prob. 12.21PCh. 12 - Problem 12.22 Draw the products formed when each...Ch. 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 - Prob. 12.32PCh. 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 - Draw the organic products formed when allylic...Ch. 12 - Draw the organic products formed in each reaction....Ch. 12 - Prob. 12.41PCh. 12 - Prob. 12.42PCh. 12 - Prob. 12.43PCh. 12 - What alkene is needed to synthesize each 1,2-diol...Ch. 12 - Prob. 12.45PCh. 12 - 12.46 (a)What product is formed in Step [1] of the...Ch. 12 - Draw the products formed after Steps 1 and 2 in...Ch. 12 - 12.48 Draw the products formed in each oxidative...Ch. 12 - What alkene or alkyne yields each set of products...Ch. 12 - Prob. 12.50PCh. 12 - Prob. 12.51PCh. 12 - Prob. 12.52PCh. 12 - Prob. 12.53PCh. 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. 12.56PCh. 12 - 12.57 Draw the product of each asymmetric...Ch. 12 - 12.58 Epoxidation of the following allylic alcohol...Ch. 12 - Prob. 12.59PCh. 12 - 12.60 Identify A in the following reaction...Ch. 12 - Prob. 12.61PCh. 12 - 12.62 It is sometimes necessary to isomerize a cis...Ch. 12 - 12.63 Devise a synthesis of each compound from...Ch. 12 - Prob. 12.64PCh. 12 - Prob. 12.65PCh. 12 - 12.66 Devise a synthesis of each compound from the...Ch. 12 - Prob. 12.67PCh. 12 - Prob. 12.68PCh. 12 - 12.69 Devise a synthesis of each compound from as...Ch. 12 - Prob. 12.70PCh. 12 - Prob. 12.71PCh. 12 - 12.72 Draw a stepwise mechanism for the following...Ch. 12 - Prob. 12.73PCh. 12 - Prob. 12.74PCh. 12 - 12.75 Sharpless epoxidation of allylic alcohol X...
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