Write the electron configuration for the first excited state for \(\mathrm{N}_{2}\) - that is, the state with the highest-energy electron moved to the next available energy level. (a) Is the nitrogen in its first excited state diamagnetic or paramagnetic? (b) Is the \(\mathrm{N}-\mathrm{N}\) bond strength in the first excited state stronger or weaker compared to that in the ground state? Explain.

Short Answer

Expert verified
The first excited state electron configuration for N₂ is \(1\sigma_g^2 1\sigma_u^2 2\sigma_g^2 2\sigma_u^2 3\sigma_g^2 1\pi_u^3 1\pi_g^1\), making it paramagnetic. The N-N bond strength in the first excited state is weaker compared to the ground state, as indicated by the bond orders (2.5 in the first excited state vs. 3 in the ground state).

Step by step solution

01

Write the ground state electron configuration of N₂

The nitrogen atom has 7 electrons. Their electron configuration in the ground state can be expressed as follows: \(1s^2 2s^2 2p^3\). In a nitrogen molecule (N₂), there are a total of 14 electrons. The electron configuration of N₂ in the ground state can be written as: \(1\sigma_g^2 1\sigma_u^2 2\sigma_g^2 2\sigma_u^2 3\sigma_g^2 1\pi_u^4\)
02

Write the electron configuration for the first excited state

To determine the first excited state of N₂, we need to move the highest-energy electron to the next available energy level. The highest-energy electron resides in the 1\(\pi_{u}\) molecular orbital. We'll move one electron from the 1\(\pi_{u}\) MO to the next available energy level, which is the 1\(\pi_{g}\) MO. This gives us the following electron configuration: \(1\sigma_g^2 1\sigma_u^2 2\sigma_g^2 2\sigma_u^2 3\sigma_g^2 1\pi_u^3 1\pi_g^1\)
03

Determine if the first excited state is diamagnetic or paramagnetic

A molecule is diamagnetic if all its electrons are paired, and it's paramagnetic if there's at least one unpaired electron. In the first excited state of N₂, the electron configuration shows that there are unpaired electrons in the 1\(\pi_{u}\) and 1\(\pi_{g}\) MOs (\(1\pi_u^3 1\pi_g^1\)). Therefore, the first excited state of N₂ is paramagnetic.
04

Compare the N-N bond strength in the first excited state to the ground state

To determine the bond strength, we look at the bond order. The bond order can be calculated using the formula: \(Bond\:Order=\frac{1}{2}(number\:of\:electrons\:in\:bonding\:orbitals - number\:of\:electrons\:in\:antibonding\:orbitals)\) For the ground state electron configuration (\(1\sigma_g^2 1\sigma_u^2 2\sigma_g^2 2\sigma_u^2 3\sigma_g^2 1\pi_u^4\)): Bond Order = \(\frac{1}{2}(10 - 4) = 3\) For the first excited state electron configuration (\(1\sigma_g^2 1\sigma_u^2 2\sigma_g^2 2\sigma_u^2 3\sigma_g^2 1\pi_u^3 1\pi_g^1\)): Bond Order = \(\frac{1}{2}(10 - 5) = 2.5\) Since the bond order for the ground state is higher than the first excited state (3 vs. 2.5), the bond strength in the ground state is stronger compared to that in the first excited state.

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Most popular questions from this chapter

Consider a molecule with formula \(\mathrm{AX}_{3}\). Supposing the \(\mathrm{A}-\mathrm{X}\) bond is polar, how would you expect the dipole moment of the \(\mathrm{AX}_{3}\) molecule to change as the \(\mathrm{X}-\mathrm{A}-\mathrm{X}\) bond angle increases from \(100^{\circ}\) to \(120^{\circ} ?\)

(a) What is the difference between a localized \(\pi\) bond and a delocalized one? (b) How can you determine whether a molecule or ion will exhibit delocalized \(\pi\) bonding? (c) Is the \(\pi\) bond in \(\mathrm{NO}_{2}^{-}\) localized or delocalized?

Predict whether each of the following molecules is polar or nonpolar: (a) IF, (b) \(\mathrm{CS}_{2}\) (c) \(\mathrm{SO}_{3}\) (d) \(\mathrm{PCl}_{3}\) (e) \(\mathrm{SF}_{6}\) (f) \(\mathrm{IF}_{5}\)

Butadiene, \(\mathrm{C}_{4} \mathrm{H}_{6}\) is a planar molecule that has the following carbocarbon bond lengths: (a) Predict the bond angles around each of the carbon atoms and sketch the molecule. (b) From left to right, what is the hybridization of each carbon atom in butadiene? (c) The middle \(C-\) bond length in butadiene \((1.48\) A) is a little shorter than the average \(\mathrm{C}-\mathrm{C}\) single bond length \((1.54 \hat{\mathrm{A}}) .\) Does this imply that the middle \(\mathrm{C}-\mathrm{Cbond}\) in butadiene is weaker or stronger than the average \(\mathrm{C}-\mathrm{C}\)? (\mathbf{d} ) Based on your answer for part ( c ),discuss what additional aspects of bonding in butadiene might support the shorter middle \(\mathrm{C}-\) C bond.

The \(\mathrm{O}-\mathrm{H}\) bond lengths in the water molecule \(\left(\mathrm{H}_{2} \mathrm{O}\right)\) are \(0.96 \AA\), and the \(\mathrm{H}-\mathrm{O}-\mathrm{H}\) angle is \(104.5^{\circ} .\) The dipole moment of the water molecule is \(1.85 \mathrm{D} .\) (a) In what directions do the bond dipoles of the \(\mathrm{O}-\mathrm{H}\) bonds point? In what direction does the dipole moment vector of the water molecule point? (b) Calculate the magnitude of the bond dipole of the \(\mathrm{O}-\mathrm{H}\) bonds. (Note: You will need to use vector addition to do this.) (c) Compare your answer from part (b) to the dipole moments of the hydrogen halides (Table 8.3). Is your answer in accord with the relative electronegativity of oxygen?

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