CHEM 281 Chapter Notes - Chapter 8: Nitromethane, Regioselectivity, Chemical Formula
6 May 2015
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Chem 281 tutorial week march 11 - march 15. What factors determine the most likely mechanism: write the expected product and the mechanism by which it forms, explain the regioselectivity of the reaction. Write its mechanism: the rate of elimination of cis-1-bromo-4-(1,1-dimethyl)cyclohexane is proportional to the concentration of both substrate and base, but that of the trans isomer is proportional only to the concentration of the substrate. Explain: when the following compound undergoes solvolysis in ethanol, three products are obtained. Propose a mechanism to account for the formation of these products. Chem 281 tutorial week march 11 - march 15: provide the products for the following three substitution reactions. For each one, indicate, in the box provided, whether the reaction is most likely to follow sn1 or. Chem 281 tutorial week march 11 - march 15: identify the compound with molecular formula c8h10o that gives the ir and 1h.
