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. Arrange the compounds in order of reactivity toward an SN2 displacement reaction. 2-chloro-2-methylbutane, 1-chloropropane, 1-chloro-2-dimethylpropane, 1-chlaro-2-methylpropane any propane N
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)
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...
Predict the substitution product(s) for each of the following reactions and mechanisms by which they are formed. If no reaction is expected, write no (a) (R)-2-bromobutane with sodium iodide in acetone (b) (R)-3-bromo-3-methylhexane with H20 (c) trans-1-bromo-2-ethylcyclopentane with potassium ethoxide in ethanol (d) trans-1-bromo-3-methylcyclopentane with Nal in acetone 5. For the following set of compounds, predict the order of reactivity with sodium iodide in acetone solution (list them in increasing order of reactivity). C. D. 2-bromobutane 1-chlorobutane 2-chloro-3-methylbutane 2-bromo-2-methylpropane 1-bromobutane...
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)
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]
Place in order of increasing E1 reactivity: Bromomethane, 2-chloropropane, 1-bromobutane, 2-bromopropane, 2-bromo-2-methylpropane
2 Number the co mpounds below in order of increasing reactivity towards Sn2 reaction. Br Cl Circle the more nucleophilic of the two species below. CII,S) CI,SII Predict the product(s) of the reactions below, showing stereochemistry of the product and the starting halide CN Br S CH3 CN CH3S
1. 3-methyl-1-butene on reaction with H-Cl forms two products, namely 2-chloro-3- methylbutane (minor) and 2-chloro-2-methylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 2. 3,3-dimethyl-1-butene on reaction with HBr forms two products, namely 3-bromo-2,2- dimethylbutane (minor) and 2-bromo-2,3-dimethylbutane (major). Illustrate the mechanism for the formation of these two products. Use curved arrows to illustrate electron movement and all intermediates must be shown. 3. Calculate...
answer all 1. In each of the following, indicate which S2 reaction will occur faster. Explain your reasoning. a. 1-bromo-2,2-dimethylpropane or 1-bromo-3-methylbutane with Nal in DMSO. b. 1-iodopentane with NaN, in ethanol or NaSCH, in ethanol, c. Reaction of isobutyl iodide with NaBr in acetone or in ethanol. 2. In each of the following, indicate which S, 1 reaction will occur faster. Explain your reasoning. a. Reaction of I-chloro-1-methylcyclohexane or 1-chloro-2-methylcyclohexane in aqueous ethanol. b. Reaction of 2-chloropentane or 3-bromohexane...