2. (4 pts) Which alkyl halide would you expect to react more rapidly by an SN2...
Indicate which alkyl halide you would expect to react more rapidly by an Si2 4 mechanism. (2 pts.) Explain your answer. (2 pts.) CI or
Which alkyl halide would you expect to react more rapidly by and SN2 mechanism? Why? 1 which alkyl halide would you expect to eact nou rapidly by an Su2 mechanism? Why? a) n. Pribor vs. t-Bu Br b) i- Buch vs. n-Buch c) Lacive. ya
3:04HS 44%. Indicate which alkyl halide you would expect to react more rapidly by mechanism. ca pts. Explain your answer. 2 pts.) S2
Which alkyl halide would you expect to react more rapidly by an Sw2 mechanism? Show products and explain your answer. 1-bromooctane or 3-bromooctane
2. Which alkyl halide would you expect to react more rapidiy by an Swi mechanism? Explain your answer. CH3 CH CI or CI Y.cl Br or (c)乂.c1 or
2. In each pair below, which alkyl halide will react more rapidly in SN1 reactions? (20 pts) (a) 1-bromobutane or tert-butyl bromide (b) 3-bromo-1-propene or 1-bromopropane
Which alkyl halide shown below would react the fastest under typical SN2 conditions?
Which alkyl halide in each of the following reactions will react faster in an SN2 reaction with hydroxide (-OH)? Explain. Hint, some of these compounds are unreactive in SN2 reactions- be sure to think about what type of alkyl halide undergoes SN2 reactions! Bromobenzene or benzyl bromide CH3Cl or (CH3)3Cl CH3CH=CHBr or H2C=CHCH2Br
a)(E)-2-nethy 2-pentene . In each pair below, which alkyl halide will react more rapidly in Sw1 reactions? (20 pts) (a) (b) 3-bromo-1-propene or 1-bromopropane 1-bromobutane or tert-butyl bromide ions(120 nts a)(E)-2-nethy 2-pentene . In each pair below, which alkyl halide will react more rapidly in Sw1 reactions? (20 pts) (a) (b) 3-bromo-1-propene or 1-bromopropane 1-bromobutane or tert-butyl bromide ions(120 nts
1. For the following Alkyl halide indicate which position will react under SN1 reaction conditions and under SN2 reaction conditions. Explain your answer. BEBE 2. Draw the complete mechanism and the products for of the following SN1 reaction paying close attention to stereochemistry. HyCc CH OH CH CHE