Which of the following energy diagrams represents the course of an exothermic SN1 reaction?

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, concerted, two step, SN1, SN2, racemization, hyperconjugation, alkyl halides, inversion):     Equilibrium favors the products of nucleophilic substitution when the leaving group is ……………. than the nucleophile.  Complete word/phrase and correct spelling (verbatim) is required. No partial credit.

Bonus question What is the IUPAC name of the compound shown below? (You need to provide complete naming; configuration, numbering, etc. No partial credit)  

Give the product(s) of the following reaction.

Which of the following energy diagrams represents the course of an endothermic SN2 reaction?

When a SN1 reaction of R-2-iodobutane takes place in methanol, the product ________.

The ΔG° (free energy change) for the conversion of A to B is predicted to be which of the following?  

Which of the following is the reaction diagram for an exothermic, concerted reaction?

How many transition states and intermediates would the reaction profile have for the reaction shown below?  

Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium cyanide, NaCN?