Exam 8: Alkenes: Structure and Preparation Via Elimination Reactions

Provide an IUPAC name for the following compound.

Draw the E isomer of 2-methyl-3-heptene.

What is (are) the most likely product(s) for the following reaction?

What are the steps of arrow pushing involved in the following mechanism?

Rank the following from most to least stable. A) B) C) D)

Which of the following is most likely to act as a base rather than a nucleophile?

Draw the major product of the following reaction.

Draw the major product of the following reaction.

Provide an IUPAC name for the following compound.

Is the following more likely a nucleophile or a base?

What is (are) the most likely product(s) for the following reaction?

Draw the mechanism and product for the following elimination.

Which of the following is most likely to act as a base rather than a nucleophile?

Draw the major organic product of the following dehydration reaction.

Is the following more likely a nucleophile or a base?

Which of the following alkenes is more stable?

Which of the following alkyl halides would afford the indicated product upon reaction with sodium ethoxide?

Rank the following from most to least stable.

Will the following alcohol be likely to undergo rearrangement during a dehydration reaction?

Draw the mechanism for the following dehydration.