Identify the nucleophilic and electrophilic sites in the substrate and reagent of the following reaction.

Which isomer(s) of 2-bromo-1,1,3-trimethylcyclohexane would be most reactive in an E2 elimination?

Which of the structures shown is most reactive in an E1 reaction?

Which reagents are appropriate to carry out the conversion shown?

Predict the product for the reaction shown.

What type of bond cleavage does the following reaction involve?

Which of the compounds shown will undergo the fastest SN1 reaction?

Assuming no other changes, what would be the effect on the rate of the reaction shown if the concentrations of both 1-chloro-3-methylbutane and NaN3 were doubled?

Select the word or phrase that complete each sentence (constitutional isomers, diastereomers, enantiomers, meso compounds, higher, lower, reaction, addition, carbocation, carbanion, nucleophile, electrophile, elimination, heterolysis, homolysis, reagent, substitution, stronger, weaker, charge, activation energy, enthalpy, entropy, catalyst, transition state, intermediate,  concerted, two step, SN1, SN2, E1, E2, racemization, hyperconjugation, alkyl halides, inversion):     On an energy diagram, each valley represents a(an) ……………………………..  Complete word/phrase and correct spelling (verbatim) is required. No partial credit.

Which of the alkyl halides shown undergoes the slowest SN1 reaction?