Rank the compounds from most reactive to least reactive under conditions of both SN1 and SN2.
Rank the compounds from most reactive to least reactive under conditions of both SN1 and SN2. Experiment CI Br 1-chl...
State whether the reaction mechanism prefers SN1 or SN2. Once sorted, rank in order from most reactive to least reactive. Experiment CI Br 1-chlorobutane 1-bromobutane 1-chloro-2-methylpropane B ta Br 2-bromobutane 2-chloro-2-methylpropane 1-chloro-2-butene 2-chlorobutane
Arrange the alkyl halides in order of reactivity (from most to least reactive) under both SN1 (silver nitrate/ethanol) and SN2 (sodium iodide/acetone) conditions: 1-bromobutane, 2-bromobutane, bromocyclohexane, 2-bromo-2-methylpropane, 1-bromoadamantane, benzyl bromide, and bromobrmzene.
Predict if the given compounds below undergo SN2 or SN1 in presence of NaI / acetone and AgNO3 / ethanol medium. (1-bromobutane, 1-chlorobutane, 2-bromobutane, 2-chlorobutane, 2-chloro-2methylpropane, 2-bromo-2-methylpropane)
Rank the following compounds from most to least reactive in an SN1 reaction.
Part A: Indicate which substrate in each pair is more reactive by an SN2 mechanism and explain why in terms of leaving group ability or substrate degree (primary, secondary, tertiary): 2-chlorobutane and 2-bromobutane 2-chlorobutane and 1-bromobutane 1-chlorobutane and 1-bromobutane 2-bromobutane and 1-bromobutane 2-chloro-2-methylpropane and 2-chlorobutane Part B: Indicate which substrate in each pair (same ones in part a) is more reactive by an SN1 mechanism and explain why in terms of leaving group ability or substrate degree (primary, secondary, tertiary).
1. Compare the reactivity of primary alkyl halides in part 1 (SN2) of this experiment to the reactivity of primary alkyl halides today. What conclusions, if any, can you make about the reactivity of these molecules under these different conditions? Use specific data to make your point. 2. Compare the reactivity of secondary alkyl halides in part 1 (SN2) of this experiment to the reactivity of secondary alkyl halides today. What conclusions, if any, can you make about the reactivity...
1) Rank the following substrates from most to least reactive in an SN2 reaction. (2 points) Br Br Br A. В. C. D.
complete the following table. Compound: Structure: 1°, 2° or 3° RX Predict reactivity (SN1, SN2, both, neither?) 1 2 3 4 5 6 1-chlorobutane 1-chloro,2-methylpropane 2-chlorobutane 2-chloro, 2-methylpropane bromobenzene benzyl bromide
Rank the following molecules in order of reactivity for an Sn2 substitution reaction (1 = most reactive, 4 = least reactive). ~ Br you d ora usea H3C-ci
15. Rank in order of Sn2 reactivity (1- most reactive) 16. Rank in order of leaving group ability (1- best leaving group) NH2 H20 CI 17. For each reaction, give the expected substitution product, and predict whether the mechanism will be predominantly first rder or second order. (a) 2-chloro-2-methylbutane CH3COOH (b) cyclohexyl bromide+ sodium ethoxide 18. Provide clear mechanism for the following reaction: CH2OCH3 Br CH3OH +HBr