The deuterium isotope (2H or D) has nearly identical reactivity as hydrogen (1H). Consequently, the one-step elimination from (R,R)-2-bromo-3-deuterobutane yields two different disubstituted alkene products. (a) Which two alkenes (A-D) could be produced by the E2 reaction of the (R,R) stereoisomer above? Major E2 product: Minor E2 product: (b) Draw the conformation of the starting halide that will lead to each product (use either Newman or sawhorse nroiectinns) (c) Could an E2 reaction with the enantiomer of (R,R)-2-bromo-deuterobutane give rise to either of the two alkenes that were NOT chosen in part (a)? Draw the enantiomer and explain. (d) Could an E2 reaction with a diastereomer of (R,R)-2-bromo-deuterobutane give rise to either of the two alkenes that were NOT chosen in part (a)? Draw a diastereomer and explain