Identify the name of the probable mechanism

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The following nucleophilic substitution reaction of (R)-3-bromo-2-methylpentane with a hydroxide ion yields 2- methylpentan-3-ol as the product. Experimental data on the rate of reaction concluded that the rate law was overall first order, dependent only on the concentration of (R)-3-bromo-2-methylpentane.

1681_figure.jpg

From this data, Identify the name of the probable mechanism:

SN1 SN2

Draw the mechanism you have chosen for this reaction in part i above.

The product(s) drawn in the mechanism must clearly show the configuration at the chiral carbon. Label the chiral carbon with that configuration.

Reference no: EM132998779

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