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Chlorination of Propane. 1 C. There are six 1 H’s and two 2 H ’s. We expect 3:1 product mix, or 75% 1-chloropropane and 25% 2-chloropropane. Typical product mix: 40% 1-chloropropane and 60% 2-chloropropane. Therefore, not all H’s are equally reactive. =>. 2 C.
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Chlorination of Propane 1 C • There are six 1 H’s and two 2 H’s. We expect 3:1 product mix, or 75% 1-chloropropane and 25% 2-chloropropane. • Typical product mix: 40% 1-chloropropane and 60% 2-chloropropane. • Therefore, not all H’s are equally reactive. => 2 C
Reactivity of Hydrogens • To compare hydrogen reactivity, find amount of product formed per hydrogen: 40% 1-chloropropane from 6 hydrogens and 60% 2-chloropropane from 2 hydrogens. • 40% 6 = 6.67% per primary H and60% 2 = 30% per secondary H • Secondary H’s are 30% 6.67% = 4.5 times more reactive toward chlorination than primary H’s. =>
Free Radical Stabilities • Energy required to break a C-H bond decreases as substitution on the carbon increases. • Stability: 3 > 2 > 1 > methylDH(kJ) 381, 397, 410, 435 =>
Chlorination Energy Diagram Lower Ea, faster rate, so more stable intermediate is formed faster. =>
Bromination of Propane 1 C 2 C • There are six 1 H’s and two 2 H’s. We expect 3:1 product mix, or 75% 1-bromopropane and 25% 2-bromopropane. • Typical product mix: 3% 1-bromopropane and 97% 2-bromopropane !!! • Bromination is more selective than chlorination. =>
Reactivity of Hydrogens • To compare hydrogen reactivity, find amount of product formed per hydrogen: 3% 1-bromopropane from 6 hydrogens and 97% 2-bromopropane from 2 hydrogens. • 3% 6 = 0.5% per primary H and97% 2 = 48.5% per secondary H • Secondary H’s are 48.5% 0.5% = 97 times more reactive toward bromination than primary H’s. =>
Bromination Energy Diagram • Note larger difference in Ea • Why endothermic? • BDE for HBr is 368 kJ, but 431 kJ for HCl =>
Hammond Postulate • Related species that are similar in energy are also similar in structure. The structure of a transition state resembles the structure of the closest stable species. • Endothermic reaction: transition state is product-like. • Exothermic reaction: transition state is reactant-like.=>