Chapter 10: Problem 54
Using your reaction roadmap as a guide, show how to convert butane into butanal. Show all reagents needed and all molecules synthesized along the way.
Chapter 10: Problem 54
Using your reaction roadmap as a guide, show how to convert butane into butanal. Show all reagents needed and all molecules synthesized along the way.
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Get started for free(a) How many stereoisomers are possible for 4 -methyl \(-1,2\)-cyclohexanediol? (b) Which of the possible stereoisomers are formed by oxidation of ( \(S)\)-4-methylcyclohexene with osmium tetroxide? (c) Is the product formed in part (b) optically active or optically inactive?
Complete the following acid-base reactions. Show all valence electrons on the interacting atoms and show by the use of curved arrows the flow of electrons in each reaction.
Dihydropyran is synthesized by treating tetrahydrofurfuryl alcohol with an arenesulfonic acid, \(\mathrm{ArSO}_{3} \mathrm{H}\). Propose a mechanism for this conversion.
The decalinols A and B can be equilibrated using aluminum isopropoxide in 2-propanol (isopropyl alcohol) containing a small amount of acetone. Assuming a value of \(\Delta G^{0}\) (equatorial to axial) for cyclohexanol is \(4.0 \mathrm{~kJ}(0.95 \mathrm{kcal}) / \mathrm{mol}\), calculate the percent of each decalinol in the equilibrium mixture at \(25^{\circ} \mathrm{C}\).
Compounds that contain an \(\mathrm{N}-\mathrm{H}\) group associate by hydrogen bonding. (a) Do you expect this association to be stronger or weaker than that of compounds containing an \(\mathrm{O}-\mathrm{H}\) group? (b) Based on your answer to part (a), which would you predict to have the higher boiling point, 1-butanol or 1-butanamine?
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