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Which hydrogen atom is most easily removed in a radical halogenation?

What is the correct order of stability of the following radicals (more stable > less stable)?

What type of reactive intermediate is formed in the reaction of propene with N-bromosuccinimide (NBS) to give 3-bromo-1-propene?

Identify the solvent that is not recommended for Green Chemistry.

What is the major product of the reaction shown below?    

What is the minimum number of steps required to convert 2-methylpropane into 1-bromo-2-methyl-2-propanol?

Select the best reagents for the reaction below.  

Rank the following radicals in order of decreasing stability, putting the most stable first.

Bonus question Reaction of compound A (molecular formula = C12H22) with ozone followed by reaction with DMS produces only (CH3)3CCH2CHO. Which of the following could be compound A?

Taxol is found in the ______ tree