🤓 Based on our data, we think this question is relevant for Professor Daoudi's class at UCF.
Which of the following statements applies to the E2 mechanism?
a) It proceeds through the more stable carbocation intermediate.
b) It occurs with racemization of stereochemistry.
c) The C-H and C-X bonds that break must be anti.
d) It occurs with inversion of stereochemistry.
e) Use of a bulky base gives the more highly substituted alkene product.