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Which of the following shows the first step for a stepwise elimination.

Which of the following statements about a two-step reaction mechanism is true?

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

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):  (   Polar protic solvents favor …………………..  mechanism.   Complete word/phrase and correct spelling (verbatim) is required. No partial credit.

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):     Alkyl halides undergo ……………………………… reactions with nucleophiles.  Complete word/phrase and correct spelling (verbatim) is required. No partial credit.

Given the following rate law, what will happen to the rate if the concentration of MeI is doubled?             Rate = k[Me3N][MeI]

What is the most reactive alkyl halide for elimination reactions?

What pattern is the second step of this reaction?

Name the following compound:  

Which of the following is the major E2 product formed from the following alkyl halide?