Química Orgánica 1 · Reacciones radicalarias y selectividad
2-Bromo-2-methylpropane by selective tertiary bromination
Condiciones: Br₂, hν
Dibuja este problema tú mismo
Arrastra desde los electrones que se mueven hasta donde van, o toca uno y luego el otro. Cada flecha se revisa; Pista te ayuda cuando te atascas. No necesitas cuenta.
El mecanismo, paso a paso
Siguiente reproduce las flechas curvas de cada paso y las explica. Los pasos escritos están abajo.
Leer los 5 pasos escritos
Initiation: split Br₂ with light
Light breaks the weak Br–Br bond homolytically: each bromine atom keeps one of the two bonding electrons, giving two neutral bromine radicals and no ions. A second Br₂ molecule waits for the propagation steps.
Las flechas curvas
- One electron of the Br–Br bond stays on the first atom.
- The other electron of the Br–Br bond stays on the second atom, so the bond splits evenly into two radicals.
Propagation: remove the tertiary hydrogen
The bromine radical removes the single tertiary hydrogen, giving the tert-butyl radical and HBr. This step decides the product: it is endothermic for bromine, so the transition state looks like the radical and strongly prefers the most stable, tertiary radical.
Las flechas curvas
- The unpaired electron on the bromine radical supplies one electron of the new bond to hydrogen.
- One electron of the tertiary C–H bond pairs with it to complete the new bond to hydrogen.
- The other tertiary C–H electron stays behind as the unpaired electron of the new radical.
Why this hydrogen?
Radical stability follows tertiary > secondary > primary > methyl, and the weakest C–H bond gives the most stable radical. Bromine is far more selective than chlorine because its abstraction step is endothermic, with a late, product-like transition state.
Propagation: take Br from a second Br₂
The carbon radical attacks Br₂, forming the C–Br bond and releasing a new bromine radical. That radical starts the next cycle, so one initiation event drives many cycles.
Las flechas curvas
- The unpaired electron on tertiary C supplies one electron of the new bond to Br.
- One electron of the Br–Br bond completes that new bond.
- The other Br–Br electron stays on the far Br, regenerating the chain-carrying radical.
2-Bromo-2-methylpropane and HBr
The tertiary carbon now carries bromine: 2-bromo-2-methylpropane. The two remaining bromine radicals either continue new chains or eventually recombine.
Qué vas a practicar
Draw Br–Br homolysis and both propagation steps that convert isobutane into 2-bromo-2-methylpropane, removing the tertiary hydrogen (2-methylpropane).
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