Chapter 9: Problem 66
Explain why the bond enthalpy of a molecule is usually defined in terms of a gas-phase reaction. Why are bond-breaking processes always endothermic and bond-forming processes always exothermic?
Chapter 9: Problem 66
Explain why the bond enthalpy of a molecule is usually defined in terms of a gas-phase reaction. Why are bond-breaking processes always endothermic and bond-forming processes always exothermic?
All the tools & learning materials you need for study success - in one app.
Get started for freeWrite Lewis structures for \(\mathrm{BrF}_{3}, \mathrm{ClF}_{5}\), and \(\mathrm{IF}_{7}\). Identify those in which the octet rule is not obeyed.
Write Lewis structures for \(\mathrm{SeF}_{4}\) and \(\mathrm{SeF}_{6}\). Is the octet rule satisfied for Se?
Most organic acids can be represented as \(\mathrm{RCOOH}\), in which \(\mathrm{COOH}\) is the carboxyl group and \(\mathrm{R}\) is the rest of the molecule. (For example, \(\mathrm{R}\) is \(\mathrm{CH}_{3}\) in acetic acid, \(\mathrm{CH}_{3} \mathrm{COOH}\).) (a) Draw a Lewis structure of the carboxyl group. (b) Upon ionization, the carboxyl group is converted to the carboxylate group, \(\mathrm{COO}^{-}\). Draw resonance structures of the carboxylate group.
Which of these molecules or ions are isoelectronic: \(\mathrm{NH}_{4}^{+}, \mathrm{C}_{6} \mathrm{H}_{6}, \mathrm{CO}, \mathrm{CH}_{4}, \mathrm{~N}_{2}, \mathrm{~B}_{3} \mathrm{~N}_{3} \mathrm{H}_{6} ?\)
Arrange these bonds in order of increasing ionic character: carbon to hydrogen, fluorine to hydrogen, bromine to hydrogen, sodium to chlorine, potassium to fluorine, lithium to chlorine.
What do you think about this solution?
We value your feedback to improve our textbook solutions.