Chapter 7: Q7-56E (page 219)
Carbocations can be stabilized by resonance. Draw all the resonance forms that would stabilize each carbocation:
Short Answer
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Chapter 7: Q7-56E (page 219)
Carbocations can be stabilized by resonance. Draw all the resonance forms that would stabilize each carbocation:
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Question: Addition of HCl to 1-isopropylcyclohexene yields a rearranged product.
Propose a mechanism, showing the structures of the intermediates and using curved arrows to indicate electron flow in each step
The isobutyl cation spontaneously rearranges to the tert-butyl cation by a hydride shift. Is the rearrangement exergonic or endergonic? Draw what you think the transition state for the hydride shift might look like according to the Hammond postulate.
Calculate the degree of unsaturation in each of the following formulas:
Which of the following compounds can exist as pairs of cis-trans isomers? Draw each cis-trans pair, and indicate the geometry of each isomer.
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