When 2,2-dimethylcyclohexanol is treated with acid, 1,2-dimethylcyclohexene and iso- propylidenecyclopentane are the products obtained. Draw a detailed mechanism that explains this result. CH3 H3O+ CH3 CH3 CH3 OH CH3 CH3 2,2-dimethyl- cyclohexanol 1,2-dimethyl- isopropylidene- cyclopentane cyclohexene

Q: Draw a mechanism for the following reaction: H3C OH H.C =CH2 CH3 七子 HO-S-OH HO

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Q: ce CH3-C=CH 2 Hce CH3-C-CH3 ce

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Q: Start from 2-methylcyclohexanol and show the steps and mechanisms for the following products.…

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Q: Draw all the products that are expected when 2-ethyl-3-methyl-1,3-cyclohexadiene is treated with HBr…

A: Draw all the products that are expected when 2-ethyl-3-methyl-1,3-cyclohexadiene is treated with HBr…

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Q: H₂C H₂C C=O acetone H H N-N H H hydrazine - H₂O H₂C H H₂C H hydrazone of acetone C=N-N

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Q: Propose a mechanism for the following reaction: CH3 CH3 CH;OH Ċ–CH3 CH3 Cl

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Q: How do you know where the benzyne take place

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Q: Propose a mechanism for this reaction. CICH,CH,OH Na,CO, H,0 H,C-CH,

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