POST-LAB QUESTIONS LAB 2 REDUCTION OF CAMPHOR 1. The ratio of borneol,1, to isoborneol, 3 , formed by the reduction of camphor was determined using 1H NMR. The hydrogen on the ring at C2 appears at 4.0ppm in borneol, whereas the analogous hydrogen in isoborneol appears at 3.6ppm. Suppose 0.316g of product was isolated and the following integration values were found: H signal at 3.6ppm:4.53 H signal at 4.0ppm:1.00 a. What percentage of the mixture was isoborneol? What percentage was borneol? ( 2 pt) b. How many mols of borneol was produced? How many mols of isoborneol were produced? (4pt) 2. Suppose you used solely your product you obtained from the first reaction, the oxidation reaction, to do the reduction reaction. And your first reaction contained starting material, (1S)-(-)-borneol, because it did not go to completion. How would that affect the outcome of the NMR results for the reduction? ( 3 pt). *Calculations must be shown to receive credit