Organic Chemistry: Principles and Mechanisms (Second Edition)
Organic Chemistry: Principles and Mechanisms (Second Edition)
2nd Edition
ISBN: 9780393663556
Author: Joel Karty
Publisher: W. W. Norton & Company
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Chapter 14, Problem 14.33P
Interpretation Introduction

(a)

Interpretation:

The bond length of the indicated C - C single bond in hexa-1, 3, 5-triene is about 146 pm, which is considerably shorter than that in ethane, H3C-CH3. It is to be determined how much shorter it is.

Concept introduction:

Weak resonance contributors give some single-bond character to the two terminal C = C bonds, resulting in the lengthening of those bonds. Resonance contributors also give some double-bond character to the C - C bond adjacent to the C = C bond, resulting in the shortening of that bond.

Expert Solution
Check Mark

Answer to Problem 14.33P

In hexa-1, 3, 5-triene, the indicated C - C single bond is shortened by about 5%.

Explanation of Solution

The bond length of C - C single bond in hexa-1, 3, 5-triene is 146 pm is shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 14, Problem 14.33P , additional homework tip  1

The normal C - C in ethane is 154 pm. Resonance contributors give some double-bond character to the C - C bond shown above, resulting in the shortening of that bond. The bond length of C - C single bond in hexa-1, 3, 5-triene is shortened by 8 pm when compared to ethane. Therefore, in hexa-1, 3, 5-triene, the indicated C - C single bond is shortened by about 5%.

Conclusion

The amount of shortening of C - C single bond in hexa-1, 3, 5-triene is determined by comparing it with the C - C single bond in ethane.

Interpretation Introduction

(b)

Interpretation:

The bond length of the indicated C - C single bond in hexa-1, 3, 5-triene is about 146 pm, which is considerably shorter than that in ethane, H3C-CH3. It is to be determined which occupied π MOs help decrease this bond length.

Concept introduction:

Resonance contributors give some double-bond character to the C - C bond adjacent to the C = C bond, resulting in the shortening of that bond. The occupied π MOs that help decrease the C - C bond length are the ones in which bonding interaction occurs.

Expert Solution
Check Mark

Answer to Problem 14.33P

The occupied π MOs that help decrease the indicated C - C bond length in hexa-1, 3, 5-triene are π1 and π2 are shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 14, Problem 14.33P , additional homework tip  2

Explanation of Solution

The bond length of C - C single bond of hexa-1, 3, 5-triene is 146 pm is shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 14, Problem 14.33P , additional homework tip  3

The occupied π MOs that help decrease the C - C bond length are the ones in which there is a bonding interaction between C2 and C3, as shown above. The three highest energy MOs do not contribute as they are not occupied. The occupied π MOs in hexa-1, 3, 5-triene are

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 14, Problem 14.33P , additional homework tip  4

Out of these, the occupied π MOs that contribute to shortening of bond between C2 and C3 include π1 and π2, as shown below:

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 14, Problem 14.33P , additional homework tip  5

Conclusion

The occupied π MOs that help decrease the indicated C - C bond length in hexa-1, 3, 5-triene are determined from the MO picture of hexa-1, 3, 5-triene.

Interpretation Introduction

(c)

Interpretation:

The bond length of the indicated C - C single bond in hexa-1, 3, 5-triene is about 146 pm, which is considerably shorter than that in ethane, H3C-CH3. It is to be explained if the length of the C - C single bond will increase, decrease, or stay roughly the same if an electron were promoted from the HOMO to the LUMO.

Concept introduction:

The highest energy MO of π bonding MOs, which are completely filled up, is generally the HOMO. The LUMO is the next highest energy unoccupied MO. The occupancy of LUMO essentially has no effect on the C - C bond if the internuclear region of the atoms of the given C - C bond shows neither a bonding nor an antibonding interaction. If the internuclear region of the HOMO shows the antibonding interaction on the removal of an electron from that orbital, the length of that C - C bond decreases.

Expert Solution
Check Mark

Answer to Problem 14.33P

If an electron were promoted from the HOMO to the LUMO, the length of the C - C single bond of hexa-1, 3, 5-triene would decrease.

Explanation of Solution

The π MOs of hexa-1, 3, 5-triene (H2C = CH - CH = CH - CH = CH2) are

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 14, Problem 14.33P , additional homework tip  6

If an electron is promoted from HOMO (π3) to LUMO (π4), the C2-C3 bond will shorten slightly. As C2-C3 internuclear region shows neither bonding nor antibonding interaction, the occupancy of LUMO has no essential effect on the bond length of the C - C single bond. The C2-C3 internuclear region of HOMO shows an antibonding interaction.

Organic Chemistry: Principles and Mechanisms (Second Edition), Chapter 14, Problem 14.33P , additional homework tip  7

Therefore, the removal of an electron from the HOMO contributes to a shorter C2-C3 bond.

Conclusion

If an electron were promoted from the HOMO to the LUMO, the length of the C - C single bond would decrease as the C2-C3 internuclear region of HOMO is an antibonding interaction.

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Chapter 14 Solutions

Organic Chemistry: Principles and Mechanisms (Second Edition)

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