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From the given structure, indicate the most stable radical.
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- Using any chemicals you like, make up a free-radical: a) Termination Step: b) Initiation Step: c) Propagation Step:PLEASE HELP DRAW THE FREE RADICAL SUBSTITUTION OF CYCLOHEXANE WHICH INOLVES THE 3 STEPS WHICH ARE initiation , propagation and terminationPlease circle the most stable radical in photo.
- Draw the most stable radical that can result from cleavage of a C–H bond in each molecule.what factor(s) might favor reactions from the generated primary radical?Fill both dashes in the paragraph Compounds containing a phenol group may work as ANTIOXIDANTS to prevent free radical damage. This is accomplished when a free radical (or UV light) encounters a phenol group, turning the phenol group into a radical. However, contrary to typical radical behavior, the structure of the phenol radical can neutralize (or quench) the unpaired electron. Specifically, the phenol structure neutralizes (or quenches) the unpaired radical electron by doing the following: taking the electron and ---------. The correct name (or abbreviation) of an example compound (discussed in the lecture videos) containing a phenol group with antioxidant properties is: ---------.