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Multiple Choice
Determine the major product(s) of the following alkane reaction. (Assume monosubstitution.)
A
B
C
D
Verified step by step guidance
1
Identify the type of reaction: The reaction involves an alkane and bromine (Br2) under heat or light (hv), indicating a free radical halogenation reaction.
Determine the possible sites for substitution: In free radical halogenation, hydrogen atoms on the alkane can be replaced by bromine. Consider the different types of hydrogen atoms present: primary, secondary, and tertiary.
Evaluate the stability of the radical intermediates: Bromine prefers to substitute at the site that forms the most stable radical. Tertiary radicals are more stable than secondary, which are more stable than primary.
Predict the major product: Given the preference for forming the most stable radical, the major product will likely involve substitution at the tertiary carbon, if available.
Consider monosubstitution: Since the problem specifies monosubstitution, only one bromine atom will replace one hydrogen atom, leading to a single major product based on the most stable radical formed.