Which of the following represents the transition state of the rate-determining step in the reaction between 2-chloropropane and sodium amide leading to elimination?

Which of the following alkyl halides undergoes the fastest SN2 reaction with sodium azide, NaN3?

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):     An SN1 mechanism forms a (an) ………………………………… as a reactive intermediate. Complete word/phrase and correct spelling (verbatim) is required. No partial credit.

What is the equation for the rate of formation of 2-methoxypropane, CH3CH(OCH3)CH3, from the reaction of 2-bromopropane (i-PrBr) with methanol?

What kind of reaction does the conversion of A to D represent?  

Given the following rate law, what will happen to the rate if the concentration of MeI is doubled?             Rate = k

Which of the following shows a mechanism for a concerted elimination.

Which of the following statements about a catalyst is true?

Which of the following anions is the most nucleophilic in polar protic solvents?

What pattern is the second step of this reaction?