Concept explainers
Estimate ΔH for the following reactions using bond energies given in Table 8.5.
3CH2=CH2(g) + 3H2(g) → 3CH2–CH3(g)
The enthalpies of formation for C6H6(g) and C6H12 (g) are 82.9 and −90.3 kJ/mol. respectively. Calculate ΔH° for the two reactions using standard enthalpies of formation from Appendix 4. Account for any differences between the results obtained from the two methods.
Interpretation:
The estimation has to be done using bond energy values and standard enthalpy of formation values.
Concept Introduction:
Enthalpy is heat content of the system. The value of enthalpy does not depend on the path of a reaction but depend on state of the system. It has a unique value for each state of the system. Thus, enthalpy is a state function. Enthalpy is represented as,
Enthalpy change, denoted by
Where
Energy required to break the existing bonds carries positive sign as energy is supplied to the system and the energy released in formation of new bonds carries negative as energy is removed from the system.
Answer to Problem 158CP
Explanation of Solution
The given reaction is,
In the above reaction, Hydrogen atoms are added to the
Energy required to break the existing bonds carries positive sign as energy is supplied to the system and the energy released in formation of new bonds carries negative as energy is removed from the system.
Accordingly, the enthalpy change for the above reaction is calculated as –
Enthalpy of formation of ethylene, hydrogen and ethane are
The term “bond energy” and “enthalpy of formation” are not similar. Bond energy refers to energy released or absorbed when isolated elements combine to form a bond. Enthalpy of formation refers to the energy released or absorbed during formation of a compound from other compounds.
Thus, enthalpy of formation of each of the compound on the reactant and product side is widely different from bond energy of the same compounds. Hence enthalpy of reaction calculated using these two different parameters is not same.
The another reaction is,
In the above reaction, Hydrogen atoms are added to the
Accordingly, the enthalpy change for the above reaction is calculated as –
Enthalpy of formation of benzene, hydrogen and cyclohexane are
As we discussed earlier, enthalpy of formation of each of the compound on the reactant and product side is widely different from bond energy of the same compounds. Hence enthalpy of reaction calculated using these two different parameters is not same.
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Chapter 22 Solutions
Student Solutions Manual for Zumdahl/Zumdahl/DeCoste?s Chemistry, 10th Edition
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- Please correct answer and don't used hand raitingarrow_forwardQ2. Consider the hydrogenation of ethylene C2H4 + H2 = C2H6 The heats of combustion and molar entropies for the three gases at 298 K are given by: C2H4 C2H6 H2 AH comb/kJ mol¹ -1395 -1550 -243 Sº / J K¹ mol-1 220.7 230.4 131.1 The average heat capacity change, ACP, for the reaction over the temperature range 298-1000 K is 10.9 J K¹ mol¹. Using these data, determine: (a) the standard enthalpy change at 800 K (b) the standard entropy change at 800 K (c) the equilibrium constant at 800 K.arrow_forward13. (11pts total) Consider the arrows pointing at three different carbon-carbon bonds in the molecule depicted below. Bond B Bond A Bond C a. (2pts) Which bond between A-C is weakest? Which is strongest? Place answers in appropriate boxes. Weakest Bond Strongest Bond b. (4pts) Consider the relative stability of all cleavage products that form when bonds A, B, AND C are homolytically cleaved/broken. Hint: cleavage products of bonds A, B, and C are all carbon radicals. i. Which ONE cleavage product is the most stable? A condensed or bond line representation is fine. ii. Which ONE cleavage product is the least stable? A condensed or bond line representation is fine. c. (5pts) Use principles discussed in lecture, supported by relevant structures, to succinctly explain the why your part b (i) radical is more stable than your part b(ii) radical. Written explanation can be no more than one-two succinct sentence(s)! Googlearrow_forward
- Print Last Name, First Name Initial Statifically more chances to abstract one of these 6H 11. (10pts total) Consider the radical chlorination of 1,3-diethylcyclohexane depicted below. 4 4th total • 6H total 래 • 4H total 21 total ZH 2H Statistical H < 3° C-H weakest - product abstraction here bund leads to thermo favored a) (6pts) How many unique mono-chlorinated products can be formed and what are the structures for the thermodynamically and statistically favored products? Product 6 Number of Unique Mono-Chlorinated Products Thermodynamically Favored Product Statistically Favored Product b) (4pts) Draw the arrow pushing mechanism for the FIRST propagation step (p-1) for the formation of the thermodynamically favored product. Only draw the p-1 step. You do not need to include lone pairs of electrons. No enthalpy calculation necessary H H-Cl Waterfoxarrow_forward10. (5pts) Provide the complete arrow pushing mechanism for the chemical transformation → depicted below Use proper curved arrow notation that explicitly illustrates all bonds being broken, and all bonds formed in the transformation. Also, be sure to include all lone pairs and formal charges on all atoms involved in the flow of electrons. CH3O II HA H CH3O-H H ①arrow_forwardDo the Lone Pairs get added bc its valence e's are a total of 6 for oxygen and that completes it or due to other reasons. How do we know the particular indication of such.arrow_forward
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