Chapter 2: Problem 58
Following are structural formulas and heats of combustion of acetaldehyde and
ethylene oxide. Which of these compounds is the more stable? Explain.
Chapter 2: Problem 58
Following are structural formulas and heats of combustion of acetaldehyde and
ethylene oxide. Which of these compounds is the more stable? Explain.
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Get started for freeDraw a chair conformation of 1,4 -dimethylcyclohexane in which one methyl group is equatorial and the other is axial. Draw the alternative chair conformation, and calculate the ratio of the two conformations at \(25^{\circ} \mathrm{C}\).
Draw line-angle formulas for the three constitutional isomers with the molecular formula \(\mathrm{C}_{5} \mathrm{H}_{12}\).
Calculate the difference in Gibbs free energy in kilojoules per mole between the alternative chair conformations of: (a) trans-4-Methylcyclohexanol (b) cis-Methylcyclohexanol (c) trans-1,4-Dicyanocyclohexane
Draw structural formulas and write IUPAC names for the nine constitutional isomers with the molecular formula \(\mathrm{C}_{7} \mathrm{H}_{16 \text { if }}\) -
Following are the alternative chair conformations for trans-1,2-dimethylcyclohexane. (a) Estimate the difference in free energy between these two conformations. (b) Given your value in (a), calculate the percent of each chair present in an equilibrium mixture of the two at \(25^{\circ} \mathrm{C}\).
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