Show how the following compounds could be prepared from 2-methylpropane:
b. 2-methyl-1-propene

Show how you would accomplish the following synthetic conversions.

(d) 2−methylbutan-2-ol → 2-bromo-3-methylbutane

Identify A through O:

Identify A–J:

Identify A–J:

The cationic polymerization of isobutylene (2-methylpropene) is shown in Section 8-16A. Isobutylene is often polymerized under free-radical conditions. Propose a mechanism for the free-radical polymerization of isobutylene.

Show how you would convert (in one or two steps) 1-phenylpropane to the three products shown below. In each case, explain what unwanted reactions might produce undesirable impurities in the product.

Show how you would synthesize each compound, starting with alkenes or cycloalkenes that contain no more than six carbon atoms. You may use any additional reagents you need.

(a)

In the following molecule, which of the labeled hydrogens ($A$, $B$, $C$, or $D$) is most easily abstracted in a free radical bromination reaction? (Assume the hydrogens are: $A$ = methyl hydrogen, $B$ = primary hydrogen, $C$ = secondary hydrogen, $D$ = tertiary hydrogen.)