1. Arrange the compounds in order of reactivity toward an SN2 displacement reaction. 2-chloro-2-methylbutane, 1-chloropropane, 1-chloro-2-dimethylpropane,...
Arrange the following chloroalkanes in order of increasing reactivity towards a S_N1 reaction: 1-chloro-2-methylbutane, 1-chloro-3-methylbutane, 2-chloro-2-methylbutane, 1-chloropentane (A complete answer will provide a bond line drawing of each of the compounds listed) For the same compounds found in question 1, list them in order of increasing reactivity towards an S_N2 reaction (list them as structures as well) Provide a bond line drawing of the product for the following reactions: (answer on back) a. (2S)-2-bromobutane + NaCN in acetone b. (3R)-3-iodo-1...
Rank (slowest to fastest) the following compounds in order of reactivity with respect to an SN2 reaction. Explain your reasoning for the ranking you propose. The compounds are 1-bromo-3-methylbutane, 1-bromo-2,2-dimethylpropane and 2-bromo-2-methylbutane.
A) 1-chloro-4-methylpentane B) 2-chloro-4-methylpentane C) 2-chloro-3-methylpentane D) 3-chloro-2-methylpentane E) 2-chloro-2-methylpentane Arrange the compounds above in order of greatest reactivity to least reactivity for an SN2 reaction [Select) [Select) [Select] [Select) [Select]
1. Draw the line structures and arrange the following substrates in order of increasing SN2 reactivity with NaCN: Bromoethane, 1-chloro-3,3-dimethylpentane, 1-chloro-2,2-dimethylpentane, and 2-bromo-2- methylpentane. (1 pt) 2. Design a synthetic route for the following conversion of methylcylohexane into compound A using retrosynthesis analysis. You may use any other reagents that you need. (1 pt) 3. Predict which of the following two compounds will undergo an E2 reaction more rapidly in presence of EtONa/EtOH. Draw the reaction product(s) and the mechanism...
A) 1-chloro-4-methylpentane B) 2-chloro-2-methylpentane C) 3-chloropentane D) 2-chloro-3-methylpentane Arrange the compounds above in order of greatest reactivity to least reactivity for an SN1 reaction. Select Select) Select Select)
Question 10 10 pts A) 1-chloro-4-methylpentane B) 2-chloro-2-methylpentane C) 3-chloropentane D) 2-chloro-3-methylpentane Arrange the compounds above in order of greatest reactivity to least reactivity for an SN 1 reaction. Select 4 | Select) • , (Select Select)
III. Correctly arrange the compounds in each set in order of decreasing reactivity toward the indicated reaction (most reactive compound first). 1.Alkyl iodide formation with HI: A. 1-hexanol B. tert-butanol C. 2-pentanol D. isopentane Answer: __________ > __________ > __________ > _________. 2. Dehydrationwith catalyticH2SO4: A. cyclopentanol B. 2-methyl-2-hexanol C. methanol D. 1-octanol Answer: __________ > __________ > __________ > _________.
1. arrange Alkyl chlorides in theoretical order of reactivity in SN1 reaction 2. arrange Alkyl chlorides in theoretical order of reactivity in SN2 reaction a HC 1-Chlorobutane AgNO3+ Ethanol (SN1) Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
1. arrange Alkyl bromides in theoretical order of reactivity in SN1 reaction 2. arrange Alkyl bromides in theoretical order of reactivity in SN2 reaction AgNO3+ Ethanol Yal H₂C (SN 1) 1-Chlorobutane Nal + Acetone SN2 CH3 H3C 2-Chlorobutane Br CH3 H3C 2-Bromobutane CH3 H2C- a CH3 t-butylchloride Benzylchloride Br Bromobenzene
Place in order of increasing E1 reactivity: Bromomethane, 2-chloropropane, 1-bromobutane, 2-bromopropane, 2-bromo-2-methylpropane