Draw the structure of
(a) A five-carbon alkene that would give the same product of HBr addition whether peroxides are present or not.
(b) A compound with the formula C6H12 that would not undergo ozonolysis.
(c) Four compounds with the formula C7H12 that would undergo catalytic hydrogenation to give methylcy- clohexane.
(d) Two alkenes that would give the following alcohol when treated with Hg(OAc)2 and H2O in THF fol-lowed by alkaline NaBH4:

(e) An alkene that would give 2-pentanone as the only product of ozonolysis followed by treatment with aqueous H2O2:

(f) The alkene that would give the following alcohol after hydroboration-oxidation :

(g) An alkene with the formula C6H12 that would give the same alcohol from either oxymercuration-reduction or hydroboration-oxidation.

Transcribed Image Text:

(CH3) CCH CH CH CH он CH,CCH CH CH 2-pentanone