Chapter 6: Problem 14
Using the table of average bond dissociation enthalpies at \(25^{\circ} \mathrm{C}\), determine which of the following reactions are energetically favorable at room temperature. Assume that \(\Delta S=0\).
Chapter 6: Problem 14
Using the table of average bond dissociation enthalpies at \(25^{\circ} \mathrm{C}\), determine which of the following reactions are energetically favorable at room temperature. Assume that \(\Delta S=0\).
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Get started for freeShow how to convert ethylene to these compounds. (a) Ethane (b) Ethanol (c) Bromoethane (d) 2-Chloroethanol (e) 1,2 -Dibromoethane (f) 1,2 -Ethanediol (g) Chloroethane
In this chapter, we studied the mechanism of the acid-catalyzed hydration of an alkene. The reverse of this reaction is the acid-catalyzed dehydration of an alcohol.
Treating cyclohexene with HBr in the presence of acetic acid gives bromocyclohexane \((85 \%)\) and cyclohexyl acetate (15\%).
The heat of hydrogenation of cis-2,2,5,5-tetramethyl-3-hexene is \(-154 \mathrm{~kJ}(-36.7 \mathrm{kcal}) /\) mol, while that of the trans isomer is only \(-113 \mathrm{~kJ}(-26.9 \mathrm{kcal}) / \mathrm{mol}\). (a) Why is the heat of hydrogenation of the cis isomer so much larger (more negative) than that of the trans isomer? (b) If a catalyst could be found that allowed equilibration of the cis and trans isomers at room temperature (such catalysts do exist), what would be the ratio of trans to cis isomers?
Predict the major organic product(s) of the following reactions and show stereochemistry where appropriate.
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