ORGANIC CHEMISTRY
ORGANIC CHEMISTRY
5th Edition
ISBN: 9781259977596
Author: SMITH
Publisher: MCG
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Chapter 13, Problem 13.37P

Propose a structure consistent with each set of data.

a. a compound that contains a benzene ring and has a molecular ion at m / z = 107

b. a hydrocarbon that contains only s p 3 hybridized carbons and a molecular ion at m / z = 84

c. a compound that contains a carbonyl group and gives a molecular ion at m / z = 114 .

d. a compound that contains C, H, N and O and has an exact mass for the molecular ion at 101.0841 .

Expert Solution
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Interpretation Introduction

(a)

Interpretation: The structure of a compound that contains a benzene ring and has a molecular ion at m/z=107 is to be proposed.

Concept introduction: Molecular mass is the sum of the atomic weights of each constituent element multiplied by the number of atoms of that element.

Answer to Problem 13.37P

The structure of the compound that contains a benzene ring and has a molecular ion at m/z=107 is,

ORGANIC CHEMISTRY, Chapter 13, Problem 13.37P , additional homework tip  1

Explanation of Solution

The molecular ion peak of a compound is observed at m/z=107.

Possible hydrocarbons are calculated as,

• Divide 107 by 12 (mass of one carbon atom). This gives the maximum number of carbon atoms.

10712=8 Carbon atoms (remainder-11)

Thus, the possible molecular formula is C8H11.

The molecular ion has odd mass. Thus, the compound may contain C, H and N atoms.

Possible compounds with C, H and N is calculated as,

• Substitute 1 N for CH2.

C8H11+1 NCH2C7H9N.

Thus, the possible molecular formula is C7H9N.

The molecular mass of C7H9N is 107. Thus, it will show molecular ion peak at m/z=107.

Hence, the structure of a compound that contains a benzene ring and has a molecular ion at m/z=107 is shown below.

ORGANIC CHEMISTRY, Chapter 13, Problem 13.37P , additional homework tip  2

Figure 1

Conclusion

The structure of a compound (C7H9N) that has a molecular ion at m/z=107 is shown in Figure 1.

Expert Solution
Check Mark
Interpretation Introduction

(b)

Interpretation: The structure of a hydrocarbon that contains only sp3 hybridized carbons and a molecular ion at m/z=84 is to be proposed.

Concept introduction: Molecular mass is the sum of the atomic weights of each constituent element multiplied by the number of atoms of that element.

Answer to Problem 13.37P

The structure of a hydrocarbon (C6H12) that contains only sp3 hybridized carbons and a molecular ion at m/z=84 is,

ORGANIC CHEMISTRY, Chapter 13, Problem 13.37P , additional homework tip  3

Explanation of Solution

The molecular ion peak of a compound is observed at m/z=84.

Possible hydrocarbons are calculated as,

• Divide 84 by 12 (mass of one carbon atom). This gives the maximum number of carbon atoms.

8412=7 Carbon atoms C7

• Replace one carbon by 12 hydrogen atoms for another possible molecular formula.

C7+12H's1CC6H12

Thus, the possible molecular formula is C6H12.

The molecular mass of C6H12 is 84. Thus, it will show molecular ion peak at m/z=84.

Hence, the structure of a hydrocarbon that contains only sp3 hybridized carbons and a molecular ion at m/z=84 is shown below.

ORGANIC CHEMISTRY, Chapter 13, Problem 13.37P , additional homework tip  4

Figure 2

Conclusion

The structure of a hydrocarbon (C6H12) that contains only sp3 hybridized carbons and a molecular ion at m/z=84 is shown in Figure 2.

Expert Solution
Check Mark
Interpretation Introduction

(c)

Interpretation: The structure of a compound that contains a carbonyl group and gives a molecular ion at m/z=114 is to be proposed.

Concept introduction: Molecular mass is the sum of the atomic weights of each constituent element multiplied by the number of atoms of that element.

Answer to Problem 13.37P

The structure of a compound (C7H14O) that gives a molecular ion at m/z=114 is,

ORGANIC CHEMISTRY, Chapter 13, Problem 13.37P , additional homework tip  5

Explanation of Solution

The molecular ion peak of a compound is observed at m/z=114.

Possible hydrocarbons are calculated as,

• Divide 114 by 12 (mass of one carbon atom). This gives the maximum number of carbon atoms.

11412=9 Carbon atoms (remainder =6)C9H6

• Replace one carbon by 12 hydrogen atoms for another possible molecular formula.

C9H6+12H's1CC8H18

The compound that contain C, H and O atoms always have a molecular ion with even mass.

Possible compounds with C, H and O is calculated as,

• Substitute 1 O for CH4.

C8H18+1 OCH4C7H14O.

Thus, the possible molecular formula is C7H14O.

Hence, the structure of a compound that contains a carbonyl group and gives a molecular ion at m/z=114 is shown below.

ORGANIC CHEMISTRY, Chapter 13, Problem 13.37P , additional homework tip  6

Figure 3

Conclusion

The structure of a compound (C7H14O) that gives a molecular ion at m/z=114 is shown in Figure 3.

Expert Solution
Check Mark
Interpretation Introduction

(d)

Interpretation: The structure of a compound that contains C, H, N and O and has an exact mass for the molecular ion at 101.0841 is to be proposed.

Concept introduction: Molecular mass is the sum of the atomic weights of each constituent element multiplied by the number of atoms of that element.

Answer to Problem 13.37P

The structure of a compound (C5H11ON) that has an exact mass for the molecular ion at 101.0841 is,

ORGANIC CHEMISTRY, Chapter 13, Problem 13.37P , additional homework tip  7

Explanation of Solution

The molecular ion peak of a compound is observed at m/z=101.

Possible hydrocarbons are calculated as,

• Divide 101 by 12 (mass of one carbon atom). This gives the maximum number of carbon atoms.

10112=8 Carbon atoms (remainder=5 )C8H5

• Replace one carbon by 12 hydrogen atoms for another possible molecular formula.

C8H5+12H's1CC7H17

The given compound contains C, H, N and O.

Possible compounds with C, H, N and O are calculated as,

• Substitute 1 O for CH4.

C7H17+1 OCH4C6H13O.

• Substitute 1 N for CH2.

C6H13O+1 NCH2C5H11ON.

Thus, the possible molecular formula is C5H11ON and exact mass of C5H11ON is 101.0841.

Hence, the structure of a compound that contains C, H, N and O and has an exact mass for the molecular ion at 101.0841 is shown below.

ORGANIC CHEMISTRY, Chapter 13, Problem 13.37P , additional homework tip  8

Figure 4

Conclusion

The structure of a compound (C5H11ON) that has an exact mass for the molecular ion at 101.0841 is shown in Figure 4.

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Chapter 13 Solutions

ORGANIC CHEMISTRY

Ch. 13 - Benzene, toluene, and p-xylene BTX are often added...Ch. 13 - Prob. 13.12PCh. 13 - Prob. 13.13PCh. 13 - Prob. 13.14PCh. 13 - Prob. 13.15PCh. 13 - How do the IR spectra of the isomers cyclopentane...Ch. 13 - Problem 13.17 How do the three isomers of...Ch. 13 - Problem 13.18 What functional groups are...Ch. 13 - Problem-13.19 What are the major IR absorptions in...Ch. 13 - Problem-13.20 What are the major IR absorptions in...Ch. 13 - Problem-13.21 Which of the following possible...Ch. 13 - Problem-13.22 Propose structures consistent with...Ch. 13 - 13.23 What major IR absorptions are present above ...Ch. 13 - Problem-13.24 The mass spectrum of the following...Ch. 13 - Prob. 13.25PCh. 13 - Which compound gives a molecular ion at m/z= 122,...Ch. 13 - Propose two molecular formulas for each molecular...Ch. 13 - Propose four possible structures for a hydrocarbon...Ch. 13 - Problem-13.29 What is the molecular formula for...Ch. 13 - Problem-13.30 Propose a molecular formula for rose...Ch. 13 - 13.31 Match each structure to its mass spectrum Ch. 13 - 13.32 Propose two possible structures for a...Ch. 13 - 13.33 What cations are formed in the mass...Ch. 13 - 13.34 and have the same molecular ion in the...Ch. 13 - 13.35 For each compound, assign likely...Ch. 13 - Prob. 13.36PCh. 13 - 13.37 Propose a structure consistent with each...Ch. 13 - 13.38 A low-resolution mass spectrum of the...Ch. 13 - 13.39 Primary alcohols often show a peak in their...Ch. 13 - 13.40 Like alcohols, ethers undergo α cleavage by...Ch. 13 - 13.41 Which of the highlighted bonds absorbs at...Ch. 13 - 13.42 What major IR absorptions are present above ...Ch. 13 - 13.43 How would each of the following pairs of...Ch. 13 - 13.44 Morphine, heroin, and oxycodone are three...Ch. 13 - 13.45 Reduction of cyclohex-2-enone can yield...Ch. 13 - Prob. 13.46PCh. 13 - 13.47 Match each compound to its IR spectrum Ch. 13 - 13.48 Propose possible structures consistent with...Ch. 13 - A chiral hydrocarbon X exhibits a molecular ion at...Ch. 13 - 13.50 A chiral compound has a strong absorption...Ch. 13 - 13.51 Treatment of benzoic acid with followed by...Ch. 13 - 13.52 Treatment of benzaldehyde with in aqueous ...Ch. 13 - Prob. 13.53PCh. 13 - 13.54 Reaction of 2-methylpropanoic acid with ...Ch. 13 - 13.55 Reaction of pentanoyl chloride with lithium...Ch. 13 - Prob. 13.56PCh. 13 - 13.57 Treatment of anisole with and forms P,...Ch. 13 - 13.58 Reaction of with forms compound ,...Ch. 13 - Problem-13.59 The carbonyl absorption of an amide...Ch. 13 - Prob. 13.60PCh. 13 - Problem-13.61 Explain why a ketone carbonyl...Ch. 13 - 13.62 Oxidation of citronellol, a constituent of...
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