6. Which Sw2 reaction of each pair would you expect to take place more rapidly? Show...
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
pls answer all Keeping in mind that carbocations have a trigonal planar structure, wwrite a structure for the carbocation intermediate AND write structures for the alcohol (or alcohols) you would expect from this reaction: 1. CH, но H Br Sy1 Which would you expect to be the stronger nucleophile: 2. a) The amid ion (NHi) or ammonia? b) RS or RSH? The reaction of methyl chloride with aqueous sodium hydroxide to produce methanol and chloride ion is essentially irreversible, proceeding...
Which SN2 reaction of each pair would you expect to take place more rapidly in polar protic solvent Aapidhy Au a n ote selmat ? a) n-PrCl aoo»?r-o- +a° vs R-Pr-O-Et Hd! -rCIEtoH Pr-o-Et t cP b) A-Prcit oo. vS. d)n- Br 4.0 M) * Heo' APia-e N-r C4-0M) eo(20M) oH
3. If sodium methoxide in methanol was used in place of potassium t butanol, your GC analysis would look much more like the 2-butanol/sulfuric acid reaction products. In addition, a new, non-alkene product would be present in the GC analysis from a competing, non-elimination mechanism. Explain why the alkene distribution would change, what the new product would be, and why this new product would form. 4. If 2-bromobutane was reacted with trimethylamine to produce sec-butyl trimethyl- ammonium bromide (see below),...
x 5. (4 pts) Predict which of the following substrates would undergo El more rapidly. . Explain your choice. 1 more rapidly year we 6. KOH (4 pts) The following Sw2 reaction yields a product with the given empirical formula. Suggest a structure for this compound and briefly show how it formed: OH mpound anderen hoe he will come to CH 120 KOH CHO MS s 2 seco 6. KOH (4 pts) The following Sw2 reaction yields a product with...
2. (4 pts) Which alkyl halide would you expect to react more rapidly by an SN2 mechanism? Explain your answer. Canna omaan " Lara
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
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
3:04HS 44%. Indicate which alkyl halide you would expect to react more rapidly by mechanism. ca pts. Explain your answer. 2 pts.) S2
11. Which of the following reactions take place more rapidly when the concentration of the nucleophile is increased? Explain your reasoning. Br + 5-CH3 – + Br