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The bond energy of a C–C single bond averages \({\rm{347 kJ mo}}{{\rm{l}}^{{\rm{ - 1}}}}\); that of a

C ≡ C triple bond averages \({\rm{839 kJ mo}}{{\rm{l}}^{{\rm{ - 1}}}}\). Explain why the triple bond is not three times as strong as a single bond.

Short Answer

Expert verified

A triple bond has an \({\rm{\sigma }}\) bond and two \({\rm{\pi }}\) bonds, whereas a single bond has only an \({\rm{\sigma }}\) bond. Because sigma bonds are far stronger than \({\rm{\pi }}\) bonds, a triple bond including one \({\rm{\sigma }}\) and two \({\rm{\pi }}\) bonds are not three times as strong as a single bond.

Step by step solution

01

Define bond energy

The amount of energy required to break apart a mole of molecules into its component atoms is known as bond energy (E). It's a metric for how strong a chemical bond is.

02

Explanation

The triple bond has an \({\rm{\sigma }}\) bond and two \({\rm{\pi }}\) bonds rather of three sigma bonds, whereas a single bond only has an \({\rm{\sigma }}\) bond. The triple bond, which consists of an \({\rm{\sigma }}\)bond and two \({\rm{\pi }}\) bonds, is not three times as strong as a single bond because sigma bonds are much stronger than \({\rm{\pi }}\) bonds.

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Most popular questions from this chapter

A useful solvent that will dissolve salts as well as organic compounds is the compound acetonitrile, \({{\rm{H}}_{\rm{3}}}{\rm{CCN}}\). It is present in paint strippers. (a) Write the Lewis structure for acetonitrile, and indicate the direction of the dipole moment in the molecule. (b) Identify the hybrid orbitals used by the carbon atoms in the molecule to form \({\rm{\sigma }}\) bonds. (c) Describe the atomic orbitals that form the \({\rm{\pi }}\) bonds in the molecule. Note that it is not necessary to hybridize the nitrogen atom.

Which of the period 2 homonuclear diatomic molecules are predicted to be paramagnetic?

Identify the hybridization of the central atom in each of the following molecules and ions that contain multiple bonds: (a) \({\rm{ClNO}}\) (\({\rm{N}}\) is the central atom) (b) \({\rm{C}}{{\rm{S}}_{\rm{2}}}\) (c) \({\rm{C}}{{\rm{l}}_{\rm{2}}}{\rm{CO}}\) (\({\rm{C}}\) is the central atom) (d) \({\rm{C}}{{\rm{l}}_{\rm{2}}}{\rm{SO}}\) (\({\rm{S}}\) is the central atom) (e) \({\rm{S}}{{\rm{O}}_{\rm{2}}}{{\rm{F}}_{\rm{2}}}\) (\({\rm{S}}\) is the central atom) (f) \({\rm{Xe}}{{\rm{O}}_{\rm{2}}}{{\rm{F}}_{\rm{2}}}\) (\({\rm{Xe}}\) is the central atom) (g) \({\rm{ClO}}{{\rm{F}}_{\rm{2}}}^{\rm{ + }}\) (\({\rm{Cl}}\) is the central atom).

Give the shape that describes each hybrid orbital set:

(a) \({\rm{s}}{{\rm{p}}^{\rm{2}}}\)

(b) \({\rm{s}}{{\rm{p}}^{\rm{3}}}{\rm{d}}\)

(c) sp

(d) \({\rm{s}}{{\rm{p}}^{\rm{3}}}{{\rm{d}}^{\rm{2}}}\)

For the carbonate ion, \({\rm{C}}{{\rm{O}}_{\rm{3}}}^{{\rm{2 - }}}\), draw all of the resonance structures. Identify which orbitals overlap to create each bond.

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