Answer Happy

Methyl chloride does NOT undergo elimination mainly because? O the carbocation formed is very unstable O the ß-carbons have occupied positions there are no ß-carbons to form double bonds O the transition state is too high in energy The reaction below will mainly produce a/an Za CI O Zaitzev anti-Zaitzev O racemic substitution product. Et O Et₂0 Which of the following alcohols reacts fastest in an acid catalyzed dehydration reaction? B. A H D. E. CH₂₁ .CH3 CH3 CH3 CH3 CH₂OH OH OH poto bo CH3 OH OH Which of the following carbonyl compounds is the most reactive? 1 / 4 / A. B. C. D.