First, bromo Ethane is the primary alkyl halides and it readily participate in SN2 reaction.
Here , bromo Ethane reacts with t- butoxide (acts as Nucleophile) and forms ethyl t-butyl ether via SN2 reaction.
From the graph, it is concluded that it is predominantly SN2 reaction.
Question 28 1 pts Imagine that a scientist mixes bromoethane and sodium tert-butoxide in 2-methyl-2-propanol. What...
Imagine that a scientist mixes bromoethane and potassium iodide in methanol. What type of reaction is likely to predominate? Remember to consider the type of alkyl halide that is involved, and remember also to consider whether the anion will act predominantly as a base or as a nucleophile or as both a base and a nucleophile. If the latter, consider the figure below to guide your decision. Finally, remember to consider the ΔpKa rule, as it applies to each of...
Consider the SN2 reaction of butyl bromide with hydroxide ion , Assuming no other changes, what effect on the reaction rate would result from simultaneously doubling the concentrations of both butyl bromide and hydroxyl ion No effect (B)It would double the rate (C)it would increase the rate six times (D) It would increase the rate four times. 2. Which alky halide would you expect to undergo SN1 hydrolysis most rapidly? (A) (CH3)3C-I (B) (CH3)3C-Br (C) (CH3)3C-Cl (D) (CH3)3C-F 3....