Author: Anonymous

Bonus question What is the product of the following reaction?  

Select the word or phrase that complete each sentence (constitutional isomers, diastereomers, enantiomers, meso compounds, higher, lower, reaction, addition, carbocation, carbanion, nucleophiles, electrophiles, elimination, heterolysis, homolysis, reagent, substitution, stronger, weaker, charge, concerted, two step, SN1, SN2, racemization, hyperconjugation, alkyl halides, inversion):  (   Strong ………………….. favor SN2 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):     Polar aprotic solvents favor …………………..  mechanism. Complete word/phrase and correct spelling (verbatim) is required. No partial credit.

What is the major product of the following E2 reaction?

Which of the following statements about bond breaking is true?

The bond dissociation energy is the amount of energy required to break a bond ________.

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

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

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?