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.
1) Determine the products of the following reactions. For the last four reactions, please indicate (a) if the reaction m
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1) Determine the products of the following reactions. For the last four reactions, please indicate (a) if the reaction m
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