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Which of the following will NOT convert 1-butanol into 1-chlorobutane in one step? A) SOCl_2 B) PCl_3 C) HCl D) CO_4 What is the first step of the mechanism for the conversion of ethanol into bromoethane using PBr_3? A) Bromide ion attacks the alcopholic carbon, displacing OH^-. B) The alcohol hydroxide group leaves, forming a carbocation. c) The alcohol oxygen attacks phosphorus, driving out bromide ion. D) One PBr_3 bromine attacks the hydroxyl hydrogen. Which reagent would be best for the conversion of tert-butanol into tert-butyl bromide? A) PBr_3 b) HBr C) NaBr D) Br_2 NaOH Give the expected major product of the following reaction. a) recovered starting material (no reaction) What is the major product of the following reaction? The Williamson ether synthesis produces ethers by reacting an A) alcohol with a metal. B) alkoxide with a metal. C) alkoxide with an alkyl halide.
Which of the following will NOT convert 1-butanol into 1-chlorobutane in one step? A) SOCl_2 B) PCl_3 C) HCl D) CO_4 What is the first step of the mechanism for the conversion of ethanol into bromoethane using PBr_3? A) Bromide ion attacks the alcopholic carbon, displacing OH^-. B) The alcohol hydroxide group leaves, forming a carbocation. c) The alcohol oxygen attacks phosphorus, driving out bromide ion. D) One PBr_3 bromine attacks the hydroxyl hydrogen. Which reagent would be best for the conversion of tert-butanol into tert-butyl bromide? A) PBr_3 b) HBr C) NaBr D) Br_2 NaOH Give the expected major product of the following reaction. a) recovered starting material (no reaction) What is the major product of the following reaction? The Williamson ether synthesis produces ethers by reacting an A) alcohol with a metal. B) alkoxide with a metal. C) alkoxide with an alkyl halide.
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Deanna HettingerLv2
3 Apr 2019
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