Chapter 4: Problem 93
The structure of \(\operatorname{Te} \mathrm{F}_{5}^{-}\) is Draw a complete Lewis structure for \(\operatorname{TeF}_{5}^{-},\) and explain the distortion from the ideal square pyramidal structure. (See Exercise 26.)
Chapter 4: Problem 93
The structure of \(\operatorname{Te} \mathrm{F}_{5}^{-}\) is Draw a complete Lewis structure for \(\operatorname{TeF}_{5}^{-},\) and explain the distortion from the ideal square pyramidal structure. (See Exercise 26.)
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Get started for freeUsing an MO energy-level diagram, would you expect \(\mathrm{F}_{2}\) to have a lower or higher first ionization energy than atomic fluorine? Why?
In which of the following diatomic molecules would the bond strength be expected to weaken as an electron is removed? a. \(\mathrm{H}_{2}\) b. \(B_{2}\) c. \(C_{2}^{2-}\) d. OF
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.
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.
Predict the molecular structure, bond angles, and polarity (has a net dipole moment or has no net dipole moment) for each of the following compounds. a. \(\mathrm{SeCl}_{4}\) b. \(\mathrm{SF}_{2}\) c. \(\mathrm{KrF}_{4}\) d. \(C B r_{4}\) e. \(\mathrm{IF}_{3}\) f. \(\mathrm{ClF}_{5}\)
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