Chapter 9: Problem 34
Sketch the Lewis structures of \(\mathrm{C} 1 \mathrm{F}_{2}^{+}\) and \(\mathrm{C} \mathrm{AF}_{2}^{-} .\) What are the electron-pair and molecular geometrics of each ion? Do both have the same \(\mathbf{F}-\mathbf{C} \mathbf{7}-\mathbf{F}\) angle? What hybrid orbital set is used by \(\mathrm{G}\) in each ion?
Short Answer
Step by step solution
Count Valence Electrons for ClF2+
Draw the Lewis Structure for ClF2+
Identify the Geometry of ClF2+
Determine the Hybridization of Cl in ClF2+
Count Valence Electrons for CAF2−
Draw the Lewis Structure for CAF2−
Identify the Geometry of CAF2−
Determine the Hybridization of CA in CAF2−
Compare F-C-F Angles
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Key Concepts
These are the key concepts you need to understand to accurately answer the question.
Valence electrons
- Chlorine (Cl) contributes 7 valence electrons.
- Each Fluorine (F) atom also contributes 7 valence electrons.
- The positive charge on the ion indicates a loss of one electron.
For \(\text{CAF}_2^-\), assuming 'CA' is a hypothetical element similar to Carbon:
- 'CA' would contribute 4 valence electrons (similar to Carbon).
- Each Fluorine atom contributes 7 electrons.
- The negative charge here means there is one extra electron.
Molecular geometry
For \(\text{ClF}_2^+\), the presence of two bonding pairs and three lone pairs on chlorine results in a molecular geometry that is **linear**. This is due to the symmetry and electronic repulsion pushing the fluorine atoms to opposite ends, making the \(\text{F-Cl-F}\) bond angle 180°. This linear shape minimizes electron pair repulsion.
In contrast, the geometry of \(\text{CAF}_2^-\) is more complex due to the assumptions and the unconventional 'central atom' used. If we consider an analogy with carbon, the expected geometry might be **bent** or **linear**, depending on electron pair distributions around the central atom and the specifics of interactions. With two bonding pairs and speculative electronic interactions, angles less than 180° could be hypothesized under certain structural conditions.
Hybridization
For \(\text{ClF}_2^+\), chlorine undergoes hybridization to accommodate its bonding and lone pairs. With five electron Agression coordinates (two bonding pairs and three lone pairs), chlorine undergoes **sp³d hybridization**. This hybrid orbital set helps to balance the repulsion between lone pairs and bonding pairs, resulting in a linear arrangement of fluorine atoms.
In the case of \(\text{CAF}_2^-\), assuming a simplistic analogy with carbon, potential hybridization is less straightforward due to assumptions and conceptualization. Normally, carbon structures with similar bonding can showcase **sp³ hybridization**. However, presence of unconventional bonding or lone pairs may invoke other hybridizations such as **sp²** or even **sp** based on specific interactions and electronic considerations. This emphasizes exploring the flexible nature of atomic interactions relying on context.
Electron-pair geometry
In \(\text{ClF}_2^+\), the electron-pair geometry is **trigonal bipyramidal** due to its five regions of electron density around the central chlorine atom. This includes two bonding pairs and three lone pairs. Despite the complex overall electron-pair geometry, the structure's linear appearance reflects the absence of lone pairs affecting bond angles between the peripheral atoms.
When considering \(\text{CAF}_2^-\), if analogous to a carbon-centered model, the potential electron-pair geometry could be linear, bent, or even influenced by unique radical characteristics based on surrounding interactions. Conventional structures might suggest minimal coordination geometries like **tetrahedral** or **trigonal planar**, expanding explorations. Without a fixed electron configuration by definition, CAF2- offers a model to explore unconventional hypothetical electron pair arrangements.