b. When 1-(1-methylethyl)cyclohexene in Et20 2-bromo-2-cyclohexylpropane mechanism using curved arrows to indicate the electron flow in each step (1-isopropylcyclohexene) is treated with a solution of HBr is the resulting product. Write the reaction and propose a

Chemistry
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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1) a. Propose a mechanism to account for the following reaction: 1-methylcyclohex-2-enol reacts
with HI to give 3-iodo-3-methylcyclohex-1-ene and 3-iodo-1-methylcyclohex-1-ene.
b. When 1-(1-methylethyl)cyclohexene (1-isopropylcyclohexene) is treated with a solution of HBr
in Et₂0 2-bromo-2-cyclohexylpropane is the resulting product. Write the reaction and propose a
mechanism using curved arrows to indicate the electron flow in each step
c. Draw a mechanism that accounts for the following transformation.
HO.
LOCH3
com
OCH3
CF3CO₂H
Transcribed Image Text:1) a. Propose a mechanism to account for the following reaction: 1-methylcyclohex-2-enol reacts with HI to give 3-iodo-3-methylcyclohex-1-ene and 3-iodo-1-methylcyclohex-1-ene. b. When 1-(1-methylethyl)cyclohexene (1-isopropylcyclohexene) is treated with a solution of HBr in Et₂0 2-bromo-2-cyclohexylpropane is the resulting product. Write the reaction and propose a mechanism using curved arrows to indicate the electron flow in each step c. Draw a mechanism that accounts for the following transformation. HO. LOCH3 com OCH3 CF3CO₂H
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