1. Explain why tertiary alcohols do not undergo oxidation. 2. Use condensed structural formulas to write the equations for the oxidation reactions of the following compounds. Write NR for products if there was no reaction. For primary alcohols, write both reaction steps. a) ethanol b) 1-butanol c) 2-butanol d) 2-methyl-2-butanol 3. Circle the more water-soluble compound in each pair. a) propane or I-propanol b) phenol or 1 -hexanol c) methanol or 1-heptanol