Answer Happy

1) Determine the products of the following reactions. For the last four reactions, please indicate (a) if the reaction mechanism is Su2, S1, E1, or E2 (note: reactions may have multiple answers) and (b) if the reacting carbon is primary. secondary, or tertiary PBr OH X Mg KBr H₂O RbOH Nal Show how you could synthesize the following compounds from an alkyl halide (note: you determine the alkyl halide used): 3-decene propylmagnesium bromide (5)-2-bromooctane a racemic mixture of 3-methylhexan-3-ol enantiomers

Sketch the reaction mechanism for your proposed synthesis in 2(c), detailing chirality center(s), transition state(s), and electron flow. Lastly, describe steric effects.