9.2 9.3 Give the structures for compounds A-D. A Cyclohexanone 1) CH3Mgl C7H140 2) H3O+ H2SO4 heat B C7H12 C D 1) BH3 in THF CrO3 C7H140 C7H120 (4) 2) H2O2, NaOH H3O+ When 1 equivalent of HBr reacts with 3-methylenecyclohexene, the first step is to protonate the two ends of the diene and draw the resonance forms of the carbocations that result. Give the structures of the likely products - show both 1,2 and 1,4 adducts. 1 mole HBr (2)
9.2 9.3 Give the structures for compounds A-D. A Cyclohexanone 1) CH3Mgl C7H140 2) H3O+ H2SO4 heat B C7H12 C D 1) BH3 in THF CrO3 C7H140 C7H120 (4) 2) H2O2, NaOH H3O+ When 1 equivalent of HBr reacts with 3-methylenecyclohexene, the first step is to protonate the two ends of the diene and draw the resonance forms of the carbocations that result. Give the structures of the likely products - show both 1,2 and 1,4 adducts. 1 mole HBr (2)
Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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