Chapter 4: Problem 119
Why do \(\mathrm{C}, \mathrm{N}, \mathrm{O},\) and \(\mathrm{F}\) atoms in covalently bonded molecules and ions have no more than eight valence electrons?
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Chapter 4: Problem 119
Why do \(\mathrm{C}, \mathrm{N}, \mathrm{O},\) and \(\mathrm{F}\) atoms in covalently bonded molecules and ions have no more than eight valence electrons?
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Skunks and Rotten Eggs Many sulfur-containing organic compounds have characteristically foul odors: butanethiol $\left(\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{SH}\right)$ is responsible for the odor of skunks, and rotten eggs smell the way they do because they produce tiny amounts of pungent hydrogen sulfide, $\mathrm{H}_{2} \mathrm{S}\(. Draw the Lewis structures for \)\mathrm{CH}_{3} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{CH}_{2} \mathrm{SH}\( and \)\mathrm{H}_{2} \mathrm{S}.$
How many valence electrons does each of the following species contain? (a) \(\mathrm{H}^{+} ;\) (b) \(\mathrm{H}_{3} \mathrm{O}^{+} ;\) (c) \(\mathrm{CO}_{2} ;\) (d) \(\mathrm{CH}_{4}.\)
Pyridine \(\left(\mathrm{C}_{5} \mathrm{H}_{5} \mathrm{N}\right)\) and pyrazine \(\left(\mathrm{C}_{4} \mathrm{H}_{4} \mathrm{N}_{2}\right)\) have structures similar to benzene. Both compounds have structures with six atoms in a ring. Draw Lewis structures for pyridine and pyrazine showing all resonance forms. The N atoms in pyrazine are across the ring from each other.
Is the ability of \(\mathrm{H}_{2} \mathrm{O}\) molecules to absorb photons of IR radiation due to symmetrical stretching or asymmetrical stretching of its \(\mathrm{O}-\mathrm{H}\) bonds, or both? Explain your answer. (Hint: The angle between the two O-H bonds in \(\left.\mathrm{H}_{2} \mathrm{O} \text { is } 104.5^{\circ} .\right).\)
Draw two Lewis structures showing the resonance that occurs in cyclobutadiene (C\(_{4} \mathrm{H}_{4}\) ), a cyclic molecule with a structure that includes a ring of four carbon atoms.
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