An energy diagram for the addition of HBr to 1-pentene is to be drawn. Both the curves, one for the formation of 1-bromopentane and another for the formation of 2-bromopentane, are to be shown in the same diagram indicating the positions of all the reactants, intermediates and products.The curve which has the higher-energy carbocation intermediate and that which has the higher-energy first transition state are to be identified. Concept introduction: The carbocation II is more stable than I. Hence it is easily formed, has less energy and its formation will be more exergonic.
An energy diagram for the addition of HBr to 1-pentene is to be drawn. Both the curves, one for the formation of 1-bromopentane and another for the formation of 2-bromopentane, are to be shown in the same diagram indicating the positions of all the reactants, intermediates and products.The curve which has the higher-energy carbocation intermediate and that which has the higher-energy first transition state are to be identified. Concept introduction: The carbocation II is more stable than I. Hence it is easily formed, has less energy and its formation will be more exergonic.
Solution Summary: The author illustrates the energy diagram for the addition of HBr to 1-pentene, indicating the positions of all the reactants, intermediates, and products. The higher-energy carbocation intermediate and the first transition state
An energy diagram for the addition of HBr to 1-pentene is to be drawn. Both the curves, one for the formation of 1-bromopentane and another for the formation of 2-bromopentane, are to be shown in the same diagram indicating the positions of all the reactants, intermediates and products.The curve which has the higher-energy carbocation intermediate and that which has the higher-energy first transition state are to be identified.
Concept introduction:
The carbocation II is more stable than I. Hence it is easily formed, has less energy and its formation will be more exergonic.
Identifying electron-donating and
For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the
benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene.
Molecule
Inductive Effects
NH2
○ donating
NO2
Explanation
Check
withdrawing
no inductive effects
Resonance Effects
Overall Electron-Density
○ donating
O withdrawing
O no resonance effects
O donating
O withdrawing
O donating
withdrawing
O no inductive effects
Ono resonance effects
O electron-rich
electron-deficient
O similar to benzene
O electron-rich
O electron-deficient
O similar to benzene
olo
18
Ar
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