Acetylene \(\left(\mathrm{C}_{2} \mathrm{H}_{2}\right)\) can be produced from the reaction of calcium carbide \(\left(\mathrm{CaC}_{2}\right)\) with water. Use both the localized electron and molecular orbital models to describe the bonding in the acetylide anion \(\left(\mathrm{C}_{2}^{2-}\right)\)

Short Answer

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In the acetylide anion (C₂²⁻), the localized electron model represents the bonding using a triple bond between the two carbon atoms and a lone pair on the negatively charged C atom. The molecular orbital model describes the bonding as a combination of σ and π orbitals, obtained from the linear combination of atomic orbitals of the two carbon atoms. These models provide two complementary ways of understanding the bonding: the localized electron model focuses on molecular connectivity and electron pairs, while the molecular orbital model focuses on the distribution and energy of electrons as a combination of atomic orbitals.

Step by step solution

01

Understanding the localized electron model

The localized electron model is a bonding model based on Lewis structures and the concept of electron pairs localized between two atoms. This model allows us to represent the molecular connectivity and emphasize the electron pairs around the atoms.
02

Describing the bonding in C₂²⁻ with the localized electron model

Using the localized electron model for the acetylide anion (C₂²⁻), we consider the Lewis structure of two C atoms. Carbon has four valence electrons, so a total of 8 electrons if we use the two C atoms. The acetylide anion has a 2- charge, meaning that there are two extra electrons making it a total of 10 electrons. Based on these 10 electrons, we can form a triple bond between the two carbon atoms, which satisfies the octet rule for each carbon atom. The remaining two electrons are localized as a lone pair on the negatively charged C atom. The Lewis structure for the acetylide anion (C₂²⁻) can be represented as: ``` C C ≡ : ``` Here, the triple bond represents the sharing of six electrons between the two carbon atoms with two electrons representing a lone pair on the rightmost carbon atom (notated with a colon).
03

Understanding the molecular orbital model

The molecular orbital model is a bonding model based on the principles of quantum mechanics that describe the distribution and energy of electrons in molecules as a combination of atomic orbitals. The molecular orbitals are a linear combination of atomic orbitals (LCAO) which can accommodate an electron pair.
04

Describing the bonding in C₂²⁻ with the molecular orbital model

We will consider the molecular orbital energies of the two carbon atoms in their ground state: 1s², 2s², 2p². The LCAO for the C₂²⁻ can be described by combining the atomic orbitals of the two carbon atoms. To analyze bonding, focus on the valence orbitals of the carbon atoms. The C₂²⁻ ion involves a linear arrangement of two carbon atoms and σ and π components. Starting with the planar σ orbitals, the 2s and one 2p orbital of each carbon atom can overlap to form σ and σ* orbitals. For the π orbitals, the remaining 2p orbitals of the carbon atoms can overlap side by side, resulting in two π and two π* orbitals. Lastly, considering the 2- negative charge of the acetylide anion, add two additional electrons to the π orbitals to obtain the correct electron configuration. C₂²⁻ Molecular Orbital Diagram: ``` π* ______ ______ π ______ ____]--> σ* _____-------> σ ______------- 2s 2p ``` The arrows indicate the filling of electrons (4 in the π orbitals and 2 in the σ orbitals) for both carbon atoms. The final configuration for the π orbitals has four electrons, while the σ component has a bonding and antibonding electron pair. In conclusion, we have described the bonding in the acetylide anion (C₂²⁻) using the localized electron model and the molecular orbital model. The localized electron model allowed us to represent the molecular connectivity and emphasize electron pairs, by featuring a triple bond and a lone pair on the rightmost carbon atom. The molecular orbital model described the distribution and energy of electrons as a combination σ and π orbitals, derived from the linear combination of atomic orbitals on the carbon atoms.

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Most popular questions from this chapter

Carbon monoxide (CO) forms bonds to a variety of metals and metal ions. Its ability to bond to iron in hemoglobin is the reason that \(\mathrm{CO}\) is so toxic. The bond carbon monoxide forms to metals is through the carbon atom: $$ \mathrm{M}-\mathrm{C} \equiv \mathrm{O} $$ a. On the basis of electronegativities, would you expect the carbon atom or the oxygen atom to form bonds to metals? b. Assign formal charges to the atoms in CO. Which atom would you expect to bond to a metal on this basis? c. In the MO model, bonding MOs place more electron density near the more electronegative atom. (See the HF molecule in Figs. 9.43 and 9.44.) Antibonding MOs place more electron density near the less electronegative atom in the diatomic molecule. Use the MO model to predict which atom of carbon monoxide should form bonds to metals.

What are the relationships among bond order, bond energy, and bond length? Which of these quantities can be measured?

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

Why are \(d\) orbitals sometimes used to form hybrid orbitals? Which period of elements does not use \(d\) orbitals for hybridization? If necessary, which \(d\) orbitals \((3 d, 4 d, 5 d, \text { or } 6 d)\) would sulfur use to form hybrid orbitals requiring \(d\) atomic orbitals? Answer the same question for arsenic and for iodine.

Describe the bonding in the first excited state of \(\mathrm{N}_{2}\) (the one closest in energy to the ground state) using the molecular orbital model. What differences do you expect in the properties of the molecule in the ground state as compared to the first excited state? (An excited state of a molecule corresponds to an electron arrangement other than that giving the lowest possible energy.)

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