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Place the species \(\mathrm{B}_{2}+, \mathrm{B}_{2}\), and \(\mathrm{B}_{2}^{-}\) in order of increasing bond length and increasing bond energy.

Short Answer

Expert verified
The species \(\mathrm{B}_{2}+, \mathrm{B}_{2}\), and \(\mathrm{B}_{2}^{-}\) can be ordered by increasing bond length as \(\mathrm{B_{2}^{+}}\), \(\mathrm{B}_{2}\), \(\mathrm{B}_{2}^{-}\) and by increasing bond energy as \(\mathrm{B}_{2}^{-}\), \(\mathrm{B}_{2}\), \(\mathrm{B_{2}^{+}}\).

Step by step solution

01

1. Determine the Total Number of Electrons in Each Species

First, let's determine the total number of electrons in each species: - \(\mathrm{B_{2}^{+}}\): Boron has 5 electrons, but this species has a positive charge, so it has lost an electron. Therefore, it has (2 × 5) - 1 = 9 electrons total. - \(\mathrm{B}_{2}\): This is a neutral molecule with each boron atom having 5 electrons, so it has 2 × 5 = 10 electrons total. - \(\mathrm{B}_{2}^{-}\): This species has a negative charge, indicating that it has gained an electron. So, it has (2 × 5) + 1 = 11 electrons total.
02

2. Fill Molecular Orbitals

Now, let's fill the molecular orbitals with electrons using the molecular orbital diagram for B₂. Use the Aufbau principle (fill lower energy orbitals first), the Pauli Exclusion Principle (maximum of 2 electrons per orbital), and Hund's rule (maximize the number of parallel spins). The molecular orbitals for B₂ are in the following order (starting from lowest energy): 1. σ(2s) 2. σ*(2s) 3. [σ(2p) and two π(2p) orbitals degenerate in energy, i.e., at the same energy level] 4. [σ(2p)* and two π*(2p) orbitals degenerate in energy] Energies of molecular orbitals decrease with increasing bond order. Bond order determines bond strength and length. Higher bond order correlates with shorter bond length and greater bond strength. Now, fill the molecular orbitals for each molecular species based on their total number of electrons: - \(\mathrm{B_{2}^{+}}\) (9 electrons): σ(2s)², σ*(2s)², σ(2p)², π(2p)³ - \(\mathrm{B}_{2}\) (10 electrons): σ(2s)², σ*(2s)², σ(2p)², π(2p)⁴ - \(\mathrm{B}_{2}^{-}\) (11 electrons): σ(2s)², σ*(2s)², σ(2p)², π(2p)⁴, σ(2p)*¹
03

3. Calculate the Bond Order

Next, we'll calculate the bond order for each species by using the formula: Bond order = (number of electrons in bonding orbitals - number of electrons in antibonding orbitals)/2 - \(\mathrm{B_{2}^{+}}\): Bond order = (6-3)/2 = 1.5 - \(\mathrm{B}_{2}\): Bond order = (6-4)/2 = 1 - \(\mathrm{B}_{2}^{-}\): Bond order = (6-5)/2 = 0.5
04

4. Order Species by Bond Length and Bond Energy

We know that higher bond order means greater bond energy (strength) and shorter bond length. Based on the bond order values we calculated, we can arrange the species as follows: - Bond length (increasing order): \(\mathrm{B_{2}^{+}}\) < \(\mathrm{B}_{2}\) < \(\mathrm{B}_{2}^{-}\) - Bond energy (increasing order): \(\mathrm{B}_{2}^{-}\) < \(\mathrm{B}_{2}\) < \(\mathrm{B_{2}^{+}}\) So, the species \(\mathrm{B}_{2}+, \mathrm{B}_{2}\), and \(\mathrm{B}_{2}^{-}\) can be ordered by increasing bond length as \(\mathrm{B_{2}^{+}}\), \(\mathrm{B}_{2}\), \(\mathrm{B}_{2}^{-}\) and by increasing bond energy as \(\mathrm{B}_{2}^{-}\), \(\mathrm{B}_{2}\), \(\mathrm{B_{2}^{+}}\).

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Bond Order
In molecular orbital theory, bond order is a crucial concept that helps us understand the strength and stability of a bond between two atoms. It is calculated using the formula: \( \text{Bond order} = \frac{\text{Number of electrons in bonding orbitals} - \text{Number of electrons in antibonding orbitals}}{2} \). A higher bond order implies a more stable and stronger bond. For instance, in our exercise, the boron molecule species \( \mathrm{B}_{2}^{+} \), \( \mathrm{B}_{2} \), and \( \mathrm{B}_{2}^{-} \) have bond orders of 1.5, 1, and 0.5, respectively. This means that \( \mathrm{B}_{2}^{+} \) is the most stable with the strongest bond, whereas \( \mathrm{B}_{2}^{-} \) is less stable with the weakest bond.
  • Higher bond order = stronger bond.
  • Lower bond order = weaker bond.
Understanding bond order allows us to predict and compare the properties of different molecular species.
Bond Length
Bond length is the distance between the nuclei of two bonded atoms. It inversely relates to bond order, meaning that a higher bond order results in a shorter bond length. In the molecular species discussed, the bond lengths can be arranged in the following order: \( \mathrm{B}_{2}^{+} < \mathrm{B}_{2} < \mathrm{B}_{2}^{-} \). This order reflects their bond orders; \( \mathrm{B}_{2}^{+} \) has the shortest bond length due to its highest bond order of 1.5, while \( \mathrm{B}_{2}^{-} \) has the longest bond length with its lowest bond order of 0.5.
  • When bond order increases, bond length decreases.
  • When bond order decreases, bond length increases.
Recognizing how bond order affects bond length helps us understand molecular geometry and reactivity.
Bond Energy
Bond energy is a measure of bond strength in a chemical bond. Higher bond energy means it takes more energy to break the bond, indicating a stronger and more stable bond. From the exercise, the bond energies of our species can be ordered as: \( \mathrm{B}_{2}^{-} < \mathrm{B}_{2} < \mathrm{B}_{2}^{+} \). This order showcases that \( \mathrm{B}_{2}^{+} \) not only has the strongest and shortest bond, but it also requires the most energy to break.
  • Higher bond energy correlates with greater bond strength.
  • Lower bond energy correlates with less bond strength.
Understanding bond energy is essential for grasping how chemical reactions occur and how much energy might be involved.

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Most popular questions from this chapter

Biacetyl and acetoin are added to margarine to make it taste more like butter. Complete the Lewis structures, predict values for all \(\mathrm{C}-\mathrm{C}-\mathrm{O}\) bond angles, and give the hybridization of the carbon atoms in these two compounds. Must the four carbon atoms and two oxygen atoms in biacetyl lie the same plane? How many \(\sigma\) bonds and how many \(\pi\) bonds are there in biacetyl and acetoin?

For each of the following molecules, write the Lewis structure(s), predict the molecular structure (including bond angles), give the expected hybrid orbitals on the central atom, and predict the overall polarity. a. \(\mathrm{CF}_{4}\) e. \(\mathrm{BeH}_{2}\) i. \(\mathrm{KrF}_{4}\) b. \(\mathrm{NF}_{3}\) f. \(\mathrm{TeF}_{4}\) j. \(\mathrm{SeF}_{6}\) c. \(\mathrm{OF}_{2}\) g. AsF \(_{5}\) k. IFs d. \(\mathrm{BF}_{3}\) h. \(\mathrm{KrF}_{2}\) L. \(\mathrm{IF}_{3}\)

Compare and contrast the MO model with the LE model. When is each useful?

Which of the following statements concerning \(\mathrm{SO}_{2}\) is(are) true? a. The central sulfur atom is \(s p^{2}\) hybridized. b. One of the sulfur-oxygen bonds is longer than the other(s). c. The bond angles about the central sulfur atom are about 120 degrees. d. There are two \(\sigma\) bonds in \(\mathrm{SO}_{2}\). e. There are no resonance structures for \(\mathrm{SO}_{2}\).

An unusual category of acids known as superacids, which are defined as any acid stronger than \(100 \%\) sulfuric acid, can be prepared by seemingly simple reactions similar to the one below. In this example, the reaction of anhydrous HF with \(\mathrm{SbF}_{5}\) produces the superacid \(\left[\mathrm{H}_{2} \mathrm{~F}\right]^{+}\left[\mathrm{SbF}_{6}\right]^{-}\) $$ 2 \mathrm{HF}(l)+\mathrm{SbF}_{5}(l) \longrightarrow\left[\mathrm{H}_{2} \mathrm{~F}\right]^{+}\left[\mathrm{SbF}_{6}\right]^{-}(l) $$ a. What are the molecular structures of all species in this reaction? What are the hybridizations of the central atoms in each species? b. What mass of \(\left[\mathrm{H}_{2} \mathrm{~F}\right]^{+}\left[\mathrm{SbF}_{6}\right]^{-}\) can be prepared when \(2.93 \mathrm{~mL}\) anhydrous \(\mathrm{HF}\) (density \(=0.975 \mathrm{~g} / \mathrm{mL}\) ) and \(10.0 \mathrm{~mL} \mathrm{SbF}_{5}\) (density \(=3.10 \mathrm{~g} / \mathrm{mL}\) ) are allowed to react?

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