Consider the \(\mathrm{H}_{2}^{+}\) ion. (a) Sketch the molecular orbitals of the ion and draw its energy-level diagram. (b) How many electrons are there in the \(\mathrm{H}_{2}^{+}\) ion? (c) Write the electron configuration of the ion in terms of its MOs. (d) What is the bond order in \(\mathrm{H}_{2}^{+}\) ? (e) Suppose that the ion is excited by light so that an electron moves from a lower-energy to a higher- energy MO. Would you expect the excited-state \(\mathrm{H}_{2}^{+}\) ion to be stable or to fall apart? (f) Which of the following statements about part (e) is correct: (i) The light excites an electron from a bonding orbital to an antibonding orbital, (ii) The light excites an electron from an antibonding orbital to a bonding orbital, or (iii) In the excited state there are more bonding electrons than antibonding electrons?

Short Answer

Expert verified
In the H₂⁺ ion, there is only one electron occupying the bonding molecular orbital (1σ) with a bond order of 1/2. When excited by light, the electron moves from the bonding to the antibonding orbital, making the excited-state H₂⁺ ion unstable. The correct statement regarding the excited state is that the light excites an electron from a bonding orbital to an antibonding orbital.

Step by step solution

01

(a) Sketch the molecular orbitals of the H₂⁺ ion and its energy-level diagram.

To sketch the molecular orbitals of the H₂⁺ ion (a hydrogen molecule with one positive charge), we need to understand that the H₂⁺ ion has two atomic orbitals from the two hydrogen atoms. When they combine, they form two molecular orbitals: one bonding and one antibonding. The bonding molecular orbital is lower in energy (more stable), while the antibonding molecular orbital is higher in energy. The energy level diagram shows these MOs with their respective energy levels.
02

(b) Number of electrons in H₂⁺ ion

In a neutral hydrogen molecule, there are two electrons, one from each hydrogen atom. However, in a H₂⁺ ion, one electron has been removed, leaving only one electron.
03

(c) Electron configuration of the ion in terms of MOs

Since there is only one electron, it will occupy the lowest energy molecular orbital, which is the bonding orbital (denoted as σ). Thus, the electron configuration is \(\mathrm{1\sigma^1}\).
04

(d) Bond order of H₂⁺ ion

The bond order is given by the formula: \(Bond\,order = \frac{1}{2} (number\, of\, electrons\,in\,bonding\,MOs - number\,of\,electrons\,in\,antibonding\,MOs)\) In the case of H₂⁺, there is only one electron in the bonding MO with none in the antibonding MO. So, the bond order is: \( \frac{1}{2} (1-0) = \frac{1}{2}\).
05

(e) Stability of excited-state H₂⁺ ion

Suppose an electron moves from a lower-energy MO to a higher-energy MO when the ion is excited by light. In this case, the electron would move from the bonding orbital to the antibonding orbital. This would result in a weaker bond or no bond at all between the hydrogen atoms. Therefore, the excited-state H₂⁺ ion would be unstable and likely to fall apart.
06

(f) Choose the correct statement about part (e)

Out of the given options, (i) The light excites an electron from a bonding orbital to an antibonding orbital, (ii) The light excites an electron from an antibonding orbital to a bonding orbital, (iii) In the excited state, there are more bonding electrons than antibonding electrons, The correct statement is (i) The light excites an electron from a bonding orbital to an antibonding orbital, because when an electron in the H₂⁺ ion becomes excited, it moves from the lower-energy (bonding) orbital to the higher-energy (antibonding) orbital, weakening or breaking the bond between hydrogen atoms.

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Most popular questions from this chapter

Sulfur tetrafluoride \(\left(\mathrm{SF}_{4}\right)\) reacts slowly with \(\mathrm{O}_{2}\) to form sulfur tetrafluoride monoxide (OSF_4) according to the following unbalanced reaction: $$ \mathrm{SF}_{4}(g)+\mathrm{O}_{2}(g) \longrightarrow \operatorname{OSF}_{4}(g) $$ The \(O\) atom and the four \(\mathrm{F}\) atoms in \(\mathrm{OSF}_{4}\) are bonded to a central S atom. (a) Balance the equation. (b) Write a Lewis structure of \(\mathrm{OSF}_{4}\) in which the formal charges of all atoms are zero. (c) Use average bond enthalpies (Table 8.3) to estimate the enthalpy of the reaction. Is it endothermic or exothermic? (d) Determine the electron-domain geometry of OSF \(_{4}\), and write two possible molecular geometries for the molecule based on this electron-domain geometry. (e) For each of the molecules you drew in part (d), state how many fluorines are equatorial and how many are axial.

(a) What is the difference between hybrid orbitals and molecular orbitals? (b) How many electrons can be placed into each MO of a molecule? (c) Can antibonding molecular orbitals have electrons in them?

Azo dyes are organic dyes that are used for many applications, such as the coloring of fabrics. Many azo dyes are derivatives of the organic substance azobenzene, \(\mathrm{C}_{12} \mathrm{H}_{10} \mathrm{~N}_{2}\) A closely related substance is hydrazobenzene, $\mathrm{C}_{12} \mathrm{H}_{12} \mathrm{~N}_{2}$ (Recall the shorthand notation used for benzene.) (a) What is the hybridization at the \(\mathrm{N}\) atom in each of the substances? (b) How many unhybridized atomic orbitals are there on the \(\mathrm{N}\) and the \(\mathrm{C}\) atoms in each of the substances? (c) Predict the \(\mathrm{N}-\mathrm{N}-\mathrm{C}\) angles in each of the substances. (d) Azobenzene is said to have greater delocalization of its \(\pi\) electrons than hydrazobenzene. Discuss this statement in light of your answers to (a) and (b). (e) All the atoms of azobenzene lie in one plane, whereas those of hydrazobenzene do not. Is this observation consistent with the statement in part (d)? (f) Azobenzene is an intense red-orange color, whereas hydrazobenzene is nearly colorless. Which molecule would be a better one to use in a solar energy conversion device? (See the "Chemistry Put to Work" box for more information about solar cells.)

Draw the Lewis structure for each of the following molecules or ions, and predict their electron-domain and molecular geometries: (a) \(\mathrm{AsF}_{3}\) (b) \(\mathrm{CH}_{3}^{+},(\mathbf{c}) \mathrm{Br} \mathrm{F}_{3}\) (d) \(\mathrm{ClO}_{3}^{-}\) (e) \(\mathrm{XeF}_{2}\) (f) \(\mathrm{BrO}_{2}^{-}\).

The structure of borazine, \(\mathrm{B}_{3} \mathrm{~N}_{3} \mathrm{H}_{6},\) is a six-membered ring of alternating \(\mathrm{B}\) and \(\mathrm{N}\) atoms. There is one \(\mathrm{H}\) atom bonded to each \(B\) and to each \(\mathrm{N}\) atom. The molecule is planar. (a) Write a Lewis structure for borazine in which the formal charge on every atom is zero. (b) Write a Lewis structure for borazine in which the octet rule is satisfied for every atom. (c) What are the formal charges on the atoms in the Lewis structure from part (b)? Given the electronegativities of \(B\) and \(N,\) do the formal charges seem favorable or unfavorable? (d) Do either of the Lewis structures in parts (a) and (b) have multiple resonance structures? (e) What are the hybridizations at the \(\mathrm{B}\) and \(\mathrm{N}\) atoms in the Lewis structures from parts (a) and (b)? Would you expect the molecule to be planar for both Lewis structures? (f) The six \(\mathrm{B}-\mathrm{N}\) bonds in the borazine molecule are all identical in length at \(144 \mathrm{pm} .\) Typical values for the bond lengths of \(\mathrm{B}-\mathrm{N}\) single and double bonds are \(151 \mathrm{pm}\) and \(131 \mathrm{pm},\) respectively. Does the value of the \(\mathrm{B}-\mathrm{N}\) bond length seem to favor one Lewis structure over the other? (g) How many electrons are in the \(\pi\) system of botazine?

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