Give the structure of the principal organic product formed by free-radical bromination of each of the following:
(a) Methylcyclopentane
(b) 1-Isopropyl-1-methylcyclopentane
(c) 2,2,4-Trimethylpentane
Sample Solution (a) Write the structure of the starting hydrocarbon, and identify any tertiary hydrogens that are present. The only tertiary hydrogen in methylcyclopentane is the one attached to C-1. This is the one replaced by bromine.
We need at least 10 more requests to produce the solution.
0 / 10 have requested this problem solution
The more requests, the faster the answer.