Answer Happy

Draw 5 constitutional isomers for the following chemical formula, make sure to draw reasonable bonding angles. CHN Draw the following mechanism. Make sure to include all appropriate arrows. Every step of the following mechanism exists in equilibrium. 2-methylbut-2-ene uses its pi bond to attack a proton from solution. A carbocation forms at the most substituted position. Water then attacks the carbocation with one of the lone pairs from oxygen. A bond forms between water and the organic molecule and the oxygen now has a positive charge. The extra proton is removed from the oxygen by an adjacent water molecule, which attacks using its lone pair of electrons, and the proton leaves behind its electrons as a new lone pair. What is the name of the resulting alcohol? Would you classify this reaction as being substitution, addition, or elimination?