The hydrolysis of sulfonates of 2-octanol is stereospecific and proceeds with complete inversion of configuration. Write a structural formula that shows the stereochemistry of the 2-octanol formed by hydrolysis of an optically pure sample of (S)-(+)-1-methylheptyl p-toluenesulfonate, identify the product as R or S, and deduce its specific rotation.

Section 5.6 (Version C) Math 112 Section: Instructor’s name: Name: 1. Suppose a culture of bacteria starts with 8000 bacteria. After one hour, the count is 9000. Find an exponential equation that models the number of bacteria in hours. Keep at least 4 decimal places in your formula for rounded values. Find the doubling time of the...