Chapter 2: Problem 4
Combine the proper prefix, infix, and suffix, and write the IUPAC name for
each compound:
(a) \(\mathrm{CH}_{3} \mathrm{CCH}_{3}\)
(b) \(\mathrm{CH}_{3}\left(\mathrm{CH}_{2}\right)_{3}{ }_{\mathrm{CH}}^{\|}\)
(c)
Chapter 2: Problem 4
Combine the proper prefix, infix, and suffix, and write the IUPAC name for
each compound:
(a) \(\mathrm{CH}_{3} \mathrm{CCH}_{3}\)
(b) \(\mathrm{CH}_{3}\left(\mathrm{CH}_{2}\right)_{3}{ }_{\mathrm{CH}}^{\|}\)
(c)
All the tools & learning materials you need for study success - in one app.
Get started for freeWrite molecular formulas for each bicycloalkane, given its number of carbon atoms. (a) Hydrindane ( 9 carbons) (b) Decalin (10 carbons) (c) Norbornane ( 7 carbons)
Draw structural formulas for the cis and trans isomers of hydrindane. Show each ring in its most stable conformation. Which of these isomers is more stable?
Following is a chair conformation of cyclohexane with the carbon atoms numbered 1 through 6 . (a) Draw hydrogen atoms that are above the plane of the ring on carbons 1 and 2 and below the plane of the ring on carbon 4 . (b) Which of these hydrogens are equatorial? Which are axial? (c) Draw the alternative chair conformation. Which hydrogens are equatorial? Which are axial? Which are above the plane of the ring? Which are below it?
Draw 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 \(25^{\circ} \mathrm{C}\).
Consider 1-bromo-2-methylpropane and draw the following. (a) The staggered conformation(s) of lowest energy (b) The staggered conformation(s) of highest energy
What do you think about this solution?
We value your feedback to improve our textbook solutions.