The reaction conditions favor the E2 mechanism. A) Draw the skeletal structure of the major organic product of the following reaction. HelpMarvin JS Edit drawing Incorrect: Your answer is incorrect. Did you remember that this reaction has a stereoelectronic conformation where the hydrogen and halogen to be eliminated adopt the anti conformation? Make sure you rotate about the single bond to get the hydrogen and halogen anti to each other then figure out the configuration of the resulting alkene. B) Select the correct statement concerning the stereochemical descriptions of this particular starting material and resultng product. (3S,4S)-3-bromo-4-methylhexane undergoes beta-elimination to give the (Z)-alkene (3R,4R)-3-bromo-4-methylhexane undergoes beta-elimination to give the (Z)-alkene (3S,4R)-3-bromo-4-methylhexane undergoes beta-elimination to give the (E)-alkene (3R,4S)-3-bromo-4-methylhexane undergoes beta-elimination to give the (Z)-alkene (3S,4R)-3-bromo-4-methylhexane undergoes beta-elimination to give the (Z)-alkene (3S,4S)-3-bromo-4-methylhexane undergoes beta-elimination to give the (E)-alkene (3R,4S)-3-bromo-4-methylhexane undergoes beta-elimination to give the (E)-alkene (3R,4R)-3-bromo-4-methylhexane undergoes beta-elimination to give the (E)-alkene