6. Thermodynamics and Kinetics
Enthalpy
- Textbook QuestionThe bromination of methane proceeds through the following steps:1. Br2 + 2 Br• ΔH° (per mole)/+190 kJ (45 kcal)Ea (per mole)/ 190 kJ (45 kcal)2. CH4 + Br• —> CH3+ HBr +73 kJ (17 kcal) 79 kJ (19 kcal) 3. • CH3 + Br2 —> CH3Br + Br -112 kJ (-27 kcal) 4 kJ (1 kcal) d. Compute the overall value of ΔH° for the bromination1views
- Multiple Choice
Predict the sign and magnitude of ∆Hoin kj/mol for the following reaction. Identify the reaction as either exothermic or endothermic.
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The combustion of alkanes is exothermic (∆H° < 0) . Would you expect the combustion of butane or cyclobutane to be more exothermic?
- Textbook Question
•CH3 + HCl → CH4 + Cl•
b. What is the activation energy for this reverse reaction?
c. What is the heat of reaction (ΔH°) for this reverse reaction?
- Textbook Question
When a small amount of iodine is added to a mixture of chlorine and methane, it prevents chlorination from occurring. Therefore, iodine is a free-radical inhibitor for this reaction. Calculate ΔH° values for the possible reactions of iodine with species present in the chlorination of methane, and use these values to explain why iodine inhibits the reaction. (The I―Cl bond-dissociation enthalpy is 211 kJ/mol or 50 kcal/mol.)
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Calculate the ∆H° value for the following reaction:
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Calculate ∆H° for the following equilibrium processes.
(b)
- Textbook Question
Iodination of alkanes using iodine (I2) is usually an unfavorable reaction. (See Problem 4-17 , for example.) Tetraiodomethane (CI4) can be used as the iodine source for iodination in the presence of a free-radical initiator such as hydrogen peroxide. Propose a mechanism (involving mildly exothermic propagation steps) for the following proposed reaction. Calculate the value of ΔH for each of the steps in your proposed mechanism.
The following bond-dissociation energies maybe helpful:
- Multiple ChoiceCalculate ΔH° for the following reaction:1views
- Textbook Question
Give the approximate bond-dissociation energy for each indicated bond.
- Textbook Question
Use bond-dissociation enthalpies (Table 4-2, p. 167) to calculate values of ΔH° for the following reactions.
b. CH3CH2Cl + HI → CH3CH2I + HCl
- Textbook Question
In the following reactions, identify the bonds formed and the bonds broken.
(a)
- Textbook Question
To this point, hydrogenation has always been an exothermic process. Using the numbers from Figure 21.6, calculate ∆Hohydr for each step of the reduction of benzene.
∆H1 + ∆H2 + ∆H3 = ∆Htot = ―49.5 kcal /mol (―208 kJ/mol)
- Textbook Question
Reactions (a) and (b) are disfavored overall (∆G° > 0), yet they are favored based on ∆H°. Identify the bonds formed and broken for (a) and (b).
(b)
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