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Given the curve

Compound A reacts with HBr/ROOR to give compound B. Compound C reacts with bromine and light to produce the same compound (compound B). What are likely structures for compounds A, B, and C?

Use the appropriate type of arrows to show the movement of electrons during the homolytic bond cleavage of ethane.

Which option correctly shows the result of a feasible addition of a radical to a π bond?

Select the synthetic sequence to accomplish the transformation shown.

Predict the major product(s) of the reaction shown.

Identify the changes that must occur to convert cis-2-butene into 2-butanol.

Propose a multi-step synthetic sequence to accomplish the transformation shown.

Which of the structures shown are monobrominated compounds (including stereoisomers) produced when 1-ethyl-4-methylbenzene is treated with NBS and UV light irradiation?

How many constitutional isomers are possible if propane is dichlorinated?