Chemistry, 21.04.2020 19:24 nssjdjsididiodododod
Be sure to answer all parts. Explain why the addition of HBr to alkenes A and C is regioselective, forming addition products B and D, respectively. 8 Addition to alkene A is regioselective because: Alkene A forms an inductively destabilized carbocation on the C closest to the O atom. Alkene A forms a resonance stabilized carbocation on the C closest to the O atom. Alkene A forms a primary carbocation, which is always more stable than a secondary carbocation. The Br atom is less crowded on a primary carbon than on a secondary carbon. Addition to alkene C is regioselective because: Alkene C forms a carbocation that is resonance stabilized by the COOCH3 group. Alkene C forms a secondary carbocation, which is always more stable than a primary carbocation. Alkene C forms a carbocation on the C farthest from the inductively destabilizing COOCH3 group. The Br atom is less crowded on the carbon that is farther away from the COOCH3 group.
Answers: 3
Chemistry, 21.06.2019 20:50, britotellerialuis
Evaluate this exponential expression,8. (2 + 3)2 – 42
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Chemistry, 22.06.2019 08:00, flakko1899
An electron moved from shell n = 2 to shell n = 1. what most likely happened during the transition? a fraction of a photon was added. a photon of energy was absorbed. a fraction of a photon was removed. a photon of energy was released.
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Be sure to answer all parts. Explain why the addition of HBr to alkenes A and C is regioselective, f...
Mathematics, 09.02.2020 23:35
Mathematics, 09.02.2020 23:35
Mathematics, 09.02.2020 23:35
Mathematics, 09.02.2020 23:35
Mathematics, 09.02.2020 23:35
Mathematics, 09.02.2020 23:36