Use the localized electron model to describe the bonding in \(\mathrm{H}_{2} \mathrm{O} .\)

Short Answer

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The bonding in $\mathrm{H}_{2}\mathrm{O}$ based on the localized electron model consists of a Lewis structure with two O-H single bonds and two lone pairs on the central oxygen atom. This results in a bent molecular geometry, with a bond angle of 104.5 degrees. The central oxygen atom is sp^3 hybridized, indicating tetrahedral electron geometry.

Step by step solution

01

Drawing the Lewis Structure

To draw the Lewis structure of water (H2O), first count the total number of valence electrons. Oxygen has 6 valence electrons and each hydrogen atom has 1 valence electron. Therefore, H2O has a total of 6 + 1 + 1 = 8 valence electrons. The least electronegative atom, oxygen, is placed in the center. We will now distribute the valence electrons as follows: 1. Place a pair of electrons between each bonded atom (oxygen and hydrogen) to form two single bonds. This accounts for 4 electrons. 2. Complete the octet rule for the central atom (oxygen) by placing the remaining 4 electrons, as lone pairs, around oxygen. The resulting Lewis structure of water is: O / \\ H - O - H | |
02

Determine the Molecular Geometry

To determine the molecular geometry of water, we count both the bonding pairs and lone pairs around the central atom (oxygen). In this case, there are 2 bonding pairs (one for each O-H bond) and 2 lone pairs. According to the VSEPR (Valence Shell Electron Pair Repulsion) theory, the geometry that minimizes the repulsion between these electron pairs is bent, with an angle of about 104.5 degrees between the H-O-H atoms.
03

Determine the Hybridization of the Central Atom

The hybridization of the central atom (oxygen) in a molecule can be determined by counting the number of electron domains around the atom. In this case, there are 4 electron domains (2 bonding pairs and 2 lone pairs) around oxygen. This corresponds to an sp^3 hybridization, where the 2s and three 2p orbitals of the oxygen atom combine to form four new, equivalent hybrid orbitals. Each hybrid orbital accommodates a single electron pair (either a bonding or lone pair), resulting in tetrahedral electron geometry with a bent molecular shape due to the lone pairs. In conclusion, the localized electron model describes the bonding in H2O as follows: 1. The Lewis structure features two O-H single bonds and two lone pairs on the central oxygen atom. 2. The resulting molecular geometry is bent, with a bond angle of 104.5 degrees. 3. The hybridization of the central oxygen atom is sp^3, according to the number of electron domains present.

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Most popular questions from this chapter

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 \(\mathrm{SO}_{2}\).

What are molecular orbitals? How do they compare with atomic orbitals? Can you tell by the shape of the bonding and antibonding orbitals which is lower in energy? Explain.

Bond energy has been defined in the text as the amount of energy required to break a chemical bond, so we have come to think of the addition of energy as breaking bonds. However, in some cases the addition of energy can cause the formation of bonds. For example, in a sample of helium gas subjected to a high-energy source, some \(\mathrm{He}_{2}\) molecules exist momentarily and then dissociate. Use MO theory (and diagrams) to explain why \(\mathrm{He}_{2}\) molecules can come to exist and why they dissociate.

The diatomic molecule OH exists in the gas phase. The bond length and bond energy have been measured to be \(97.06 \mathrm{pm}\) and \(424.7 \mathrm{~kJ} / \mathrm{mol}\), respectively. Assume that the \(\mathrm{OH}\) molecule is analogous to the HF molecule discussed in the chapter and that molecular orbitals result from the overlap of a lowerenergy \(p_{z}\) orbital from oxygen with the higher-energy \(1 s\) orbital of hydrogen (the \(\mathrm{O}-\mathrm{H}\) bond lies along the \(z\) -axis). a. Which of the two molecular orbitals will have the greater hydrogen \(1 s\) character? b. Can the \(2 p_{x}\) orbital of oxygen form molecular orbitals with the \(1 s\) orbital of hydrogen? Explain. c. Knowing that only the \(2 p\) orbitals of oxygen will interact significantly with the \(1 s\) orbital of hydrogen, complete the molecular orbital energy- level diagram for \(\mathrm{OH}\). Place the correct number of electrons in the energy levels. d. Estimate the bond order for OH. e. Predict whether the bond order of \(\mathrm{OH}^{+}\) will be greater than, less than, or the same as that of OH. Explain.

Why does the molecular orbital model do a better job in explaining the bonding in \(\mathrm{NO}^{-}\) and \(\mathrm{NO}\) than the hybrid orbital model?

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