Chapter 3: Problem 14
Why do we call \(\mathrm{Ba}\left(\mathrm{NO}_{3}\right)_{2}\) barium nitrate, but we call \(\mathrm{Fe}\left(\mathrm{NO}_{3}\right)_{2}\) iron(II) nitrate?
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Chapter 3: Problem 14
Why do we call \(\mathrm{Ba}\left(\mathrm{NO}_{3}\right)_{2}\) barium nitrate, but we call \(\mathrm{Fe}\left(\mathrm{NO}_{3}\right)_{2}\) iron(II) nitrate?
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Consider the following bond lengths: \(\begin{array}{cccccc}\mathbf{C}-\mathbf{O} & 143 \mathrm{pm} & \mathbf{C}=\mathbf{O} & 123 \mathrm{pm} & \mathbf{C} \equiv \mathbf{O} & 109 \mathrm{pm}\end{array}\) In the \(\mathrm{CO}_{3}^{2-}\) ion, all three \(\mathrm{C}-\mathrm{O}\) bonds have identical bond lengths of \(136 \mathrm{pm}\). Why?
Without using Fig. \(3-4,\) predict which bond in each of the following groups will be the most polar. a. \(\mathrm{C}-\mathrm{H}, \mathrm{Si}-\mathrm{H}, \mathrm{Sn}-\mathrm{H}\) \(\mathbf{b .}\) Al- \(\mathbf{B r}, \mathbf{G a}-\mathbf{B r}, \operatorname{In}-\mathbf{B r}, \mathbf{T}-\mathbf{B r}\) c. \(C-O\) or \(S i-O\) d. \(\mathrm{O}-\mathrm{F}\) or \(\mathrm{O}-\mathrm{Cl}\)
Write electron configurations for the most stable ion formed by each of the elements Te, \(\mathrm{Cl}, \mathrm{Sr},\) and \(\mathrm{Li}\) (when in stable ionic compounds).
Lewis structures can be used to understand why some molecules react in certain ways. Write the Lewis structures for the reactants and products in the reactions described below. a. Nitrogen dioxide dimerizes to produce dinitrogen tetroxide. b. Boron trihydride accepts a pair of electrons from ammonia, forming \(\mathrm{BH}_{3} \mathrm{NH}_{3}\) Give a possible explanation for why these two reactions occur.
Nitrous oxide \(\left(\mathrm{N}_{2} \mathrm{O}\right)\) has three possible Lewis structures: $$\therefore N=N=O^{\cdot} \leftrightarrow: N \equiv N-\vec{O}: \longleftrightarrow: N-N \equiv 0$$ Given the following bond lengths, $$\begin{aligned} &\mathrm{N}-\mathrm{N} \quad 167 \mathrm{pm} \quad \mathrm{N}=\mathrm{O} \quad 115 \mathrm{pm}\\\ &\mathrm{N}=\mathrm{N} \quad 120 \mathrm{pm} \quad \mathrm{N}-\mathrm{O} \quad 147 \mathrm{pm}\\\ &\mathrm{N} \equiv \mathrm{N} \quad 110 \mathrm{pm} \end{aligned}$$ rationalize the observations that the \(\mathrm{N}-\mathrm{N}\) bond length in \(\mathrm{N}_{2} \mathrm{O}\) is \(112 \mathrm{pm}\) and that the \(\mathrm{N}-\mathrm{O}\) bond length is \(119 \mathrm{pm}\). Assign formal charges to the resonance structures for \(\mathrm{N}_{2} \mathrm{O}\). Can you eliminate any of the resonance structures on the basis of formal charges? Is this consistent with observation?
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