Blog

What type of bond cleavage takes place in/what type of intermediate is produced in the following reaction?

What is the major product of the following E2 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 following compound? (You need to provide complete naming; R/S configuration, numbering, etc. 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.

Bonus question What is the IUPAC name of the compound shown below? (You need to provide complete naming; 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 ________.

What is the major elimination product obtained from the following reaction?