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Alcohols and ethers are more reactive to substitution and elimination reactions under acidic conditions (compared to basic or neutral conditions). Draw the product of the reaction of the molecule shown with a strong acid. 0 0 0 1 Which structure from Part 1 would have a better leaving group: the reactant or the product? Choose one: O A. The product would have a better leaving group. O B. The reactant would have a better leaving group. C. Neither structure would have a good leaving group. O D. Both structures have equally good leaving groups. Draw the expected product when the protonated alcohol (the product) from part one reacts with iodide ion. ⒸO +1

Alcohols and ethers are more reactive to substitution and elimination reactions under acidic conditions (compared to basic or neutral conditions). Draw the product of the reaction of the molecule shown with a strong acid. 0 0 0 1 Which structure from Part 1 would have a better leaving group: the reactant or the product? Choose one: O A. The product would have a better leaving group. O B. The reactant would have a better leaving group. C. Neither structure would have a good leaving group. O D. Both structures have equally good leaving groups. Draw the expected product when the protonated alcohol (the product) from part one reacts with iodide ion. ⒸO +1

Chemistry by OpenStax (2015-05-04)
Chemistry by OpenStax (2015-05-04)
1st Edition
ISBN:9781938168390
Author:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Publisher:Klaus Theopold, Richard H Langley, Paul Flowers, William R. Robinson, Mark Blaser
Chapter20: Organic Chemistry
Section: Chapter Questions
Problem 48E: The foul odor of rancid butter is caused by butyric acid, CH3CH2CH2CO2H. (a) Draw the Lewis...
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Alcohols and ethers are more reactive to substitution and elimination reactions under acidic conditions (compared to basic or neutral conditions). Draw the product of the reaction of the molecule shown with a strong acid. O ² ⒸO +1 Which structure from Part 1 would have a better leaving group: the reactant or the product? Choose one: O A. The product would have a better leaving group. OB. The reactant would have a better leaving group. C. Neither structure would have a good leaving group. O D. Both structures have equally good leaving groups. Draw the expected product when the protonated alcohol (the product) from part one reacts with iodide ion. DOC 20+1 H CI Br H C F P Cl Br I
Transcribed Image Text:Alcohols and ethers are more reactive to substitution and elimination reactions under acidic conditions (compared to basic or neutral conditions). Draw the product of the reaction of the molecule shown with a strong acid. O ² ⒸO +1 Which structure from Part 1 would have a better leaving group: the reactant or the product? Choose one: O A. The product would have a better leaving group. OB. The reactant would have a better leaving group. C. Neither structure would have a good leaving group. O D. Both structures have equally good leaving groups. Draw the expected product when the protonated alcohol (the product) from part one reacts with iodide ion. DOC 20+1 H CI Br H C F P Cl Br I
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