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...
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 is needed to produce leucine from Gabriel synthesis? 1-bromo-2-methylpropane 2-bromobutane 2-bromopropane bromomethane
for each pair of compounds, state which is the better SN2 substrate 2-methyl-1-iodopropane or tert-butyl iodide 2-methyl-1-iodopropane O tert-butyl iodide Submit Request Answer Part B cyclohexyl bromide or 1-bromo-1-methylcyclohexane 1-bromo-1-methylcyclohexane cyclohexyl bromide 2-bromobutane or isopropyl bromide O isopropyl bromide 2-bromobutane Submit Request Answer Part D 1-chloro-2,2-dimethylbutane or 2-chlorobutane O 1-chloro-2,2-dimethylbutane 2-chlorobutane 1-iodobutane or 2-iodopropane O 2-iodopropane O 1-iodobutane Submit Request Answer
2. (4 pts) Which alkyl halide would you expect to react more rapidly by an SN2 mechanism? Explain your answer. Canna omaan " Lara
() 1. Which of the following alkyl holides would you expect to be most reactive in a unimolecular reaction? CH3 a) CsM , CH, CH, CH, Br b) CEHCH CH BY c) CH, CCH, Br d) CH, CH2 CH CHE сн. он сня Br e) CHICCHE CH3 (4). 2. What would you expect to be the chief organic product(s) when tert-butyl bromide reacts with sodium acetylide, i.e.. CH + - CH3-C-Br + Na CECH ? CH a) 1 b) II...
Part 2 Multiple Choice. Select the best answer for each of the questions below: 1. Which of these molecules is not an electrophile? a) CH4 b) CH3+ c) H* d) BF3 2. Which of these molecules is not a nucleophile ? a) NH3 b) OH c) CN d) H* 3. Water behaves as: a) a nucleophile b) an electrophile c) both d) neither 4. The SN2 reaction has how many steps? a) 1 b) 2 c) 3 d) 4 5....
CH3 (4) 1. Which of the following alkyl halides would you expect to be most reactive in a unimolecular reaction? a) C&H, CH, CH, CH, BY b) CH 1 CH CH Br C) CH11CCH, Br d) C6H CH2 CH CHỊ CHỊ CH3 CHỊ e) C&H, CCH Br CHE (4) 2. What would you expect to be the chief organic product(s) when tert-butyl bromide reacts with sodium acetylide, i.e., CH3 + - CH2-C-Br + Na :CECH — ? CH a) I...
1. [10 pts] Consider the elimination reaction for the following alkyl halide with sodium methoxide in methanol (Na* OCH, CH,OH). CH NaOme MeOH CH Compound A Problem 2c Draw the major expected organic product (a) Redraw Compound A as seen in Viewpoint I below left as a Newman projection on the template provided in Problem 2a (below). Hint: Fill in missing Hs ar C2 and C3 to help you get started! (b) Rotate the C2 C3 bond to obtain the...
1. In both the sodium iodide test and the silver nitrate test, why does 2-bromobutane react faster than 2-chlorobutane? Bromine is a better leaving group since it is a weaker base than chlorine is. 2. a. Why does benzyl chloride react under both SN1 and SN2 conditions? Benzyl chloride is a primary alkyl halide, hence reactive under SN2 conditions. The primary carbocation formed due to the departure of Cl- is stabilized by the pi electrons in the benzene ring. b. Why is...