when 2-methyl-2-butanol undergoes an acid-catalyzed dehydration, a number of alkene products are possibly formed.
Please solve both questions (top and bottom one) and show your work (I would really appreciate it as I am a little confused and have been trying)
PRELAB 2. When 2-methyl-2-b utanol undergoes an acid-catalyzed dehydration, a number of alkene products are possibly formed. Does this reaction proceed by an El or an E2 mechanism? acid and draw an "arrow pushing" mechanism (one that uses curly arrows) for the formation of the prod . Draw the products, including all stereoisomers, of the following reactions.
