Why must all six atoms in \(\mathrm{C}_{2} \mathrm{H}_{4}\) lie in the same plane?

Short Answer

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All six atoms in \(\mathrm{C}_{2} \mathrm{H}_{4}\) (ethene) must lie in the same plane due to the planar arrangement of the sp2 hybrid orbitals and the formation of a pi (π) bond between the carbon atoms. The carbon atoms in ethene are sp2 hybridized, having three sp2 hybrid orbitals in a trigonal planar geometry with bond angles of approximately 120°. These orbitals form sigma (σ) bonds with the hydrogen atoms, which also lie in the same plane. Additionally, the pi (π) bond between the carbon atoms is formed by the overlap of their unhybridized p orbitals, which are perpendicular to the plane of the sp2 hybrid orbitals.

Step by step solution

01

Understand the molecular formula of \(\mathrm{C}_{2} \mathrm{H}_{4}\)

In the given molecular formula, there are two carbon atoms (C) and four hydrogen atoms (H). This molecule is called ethene. Now, let's determine the structure of the ethene molecule with the help of hybridization.
02

Determine the hybridization of carbon atoms in ethene

To determine the hybridization of the carbon atoms, we first need to know the number of sigma (σ) bonds and valence electrons of each carbon atom. Carbon has four valence electrons and needs to form four bonds to achieve an octet configuration. Ethene has a double bond between the two carbon atoms and each carbon atom is bonded to two hydrogen atoms. Thus, each carbon atom forms three sigma (σ) bonds: one with the other carbon atom and two with hydrogen atoms. The double bond between the carbon atoms consists of one sigma (σ) bond and one pi (π) bond. Now, let's apply the formula for hybridization: \(hybridization = \frac{number\,of\,σ\,bonds + number\,of\,lone\,pair\,electrons}{2}\) For each carbon atom in ethene: \(hybridization = \frac{3\,σ\,bonds + 0\,lone\,pair\,electrons}{2} = \frac{3}{2}\) Since the value is greater than 1 and less than or equal to 2, the hybridization of each carbon atom is sp2.
03

Describe the geometry of sp2 hybridized carbon atoms

In sp2 hybridization, one s and two p orbitals of the carbon atom mix to form three new sp2 hybrid orbitals. These orbitals arrange themselves in a trigonal planar geometry with bond angles of approximately 120°. The remaining p orbital, which is not involved in the hybridization, lies perpendicular to the plane of the sp2 hybrid orbitals.
04

Explain the planar geometry of ethene (\(\mathrm{C}_{2} \mathrm{H}_{4}\))

Now that we know the hybridization and geometry of the carbon atoms in ethene, we can explain why all six atoms must lie in the same plane. The two carbon atoms and the four hydrogen atoms form sigma (σ) bonds using their sp2 hybrid orbitals. Since these sp2 hybrid orbitals are arranged in a trigonal planar geometry around each carbon atom, all the atoms bonded to the carbon atoms also lie in the same plane. Furthermore, the pi (π) bond between the two carbon atoms is formed by the overlap of the unhybridized p orbitals of the carbon atoms, which are perpendicular to the plane of the sp2 hybrid orbitals. This further supports the planar geometry of the ethene molecule. Thus, all six atoms in \(\mathrm{C}_{2} \mathrm{H}_{4}\) (ethene) must lie in the same plane because of the planar arrangement of the sp2 hybrid orbitals and the formation of a pi (π) bond between the carbon atoms.

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Most popular questions from this chapter

Using molecular orbital theory, explain why the removal of one electron in \(\mathrm{O}_{2}\) strengthens bonding, while the removal of one electron in \(\mathrm{N}_{2}\) weakens bonding.

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

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 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 1s 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 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.

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