The radical fluorination of 2-methyl propane resulted in a 14:86 ratio of products.

(a) On the basis of this ratio, calculate the relative reactivity of 1° and 3° C―H bonds in the radical fluorination.

For each alkane,

3. which monobrominated derivatives could you form in good yield by free-radical bromination?

c. 2-methylpentane

d. 2,2,3,3-tetramethylbutane

For each alkane,

1. draw all the possible monochlorinated derivatives.

c. 2-methylpentane

d. 2,2,3,3-tetramethyl butane

The chlorination of pentane gives a mixture of three monochlorinated products.

a. Draw their structures.

Predict the major monohalogenation product(s) of the following reactions. Indicate whether you think the reaction will be selective and justify your position.

(a)

The radical fluorination of 2-methyl propane resulted in a 14:86 ratio of products.

(b) From the relative reactivity, calculate the difference in energy between the transition states of the first propagation steps leading to a 1° and 3° radical.

Show how free-radical halogenation might be used to synthesize the following ­compounds. In each case, explain why we expect to get a single major product.

(a) 1-chloro-2,2-dimethylpropane (neopentyl chloride)

(b) 2-bromo-2-methylbutane

Rationalize the fact that reaction A results in an unequal mixture of products, but reaction B yields an equal mixture of two products.

Because of the angle strain present in cyclopropanes, they tend to open up in the presence of nearby radicals. Show a mechanism for the following reaction that demonstrates this principle.