(A) SNl reactions are stepwise and have intermediates. (B) The slow step in a Syl reaction is formation of the carbocation intermediate. (C) SNl reactions have first order kinetics which means only the alkyl halide is involved in the rate limiting step. (D) The products of a Syl reaction will be a pair of enantiomers. (E) An aprotic solvent is best for Snl reactions as they tend to help stabilize carbocation intermediates.
(A) SNl reactions are stepwise and have intermediates. (B) The slow step in a Syl reaction is formation of the carbocation intermediate. (C) SNl reactions have first order kinetics which means only the alkyl halide is involved in the rate limiting step. (D) The products of a Syl reaction will be a pair of enantiomers. (E) An aprotic solvent is best for Snl reactions as they tend to help stabilize carbocation intermediates.
Chemistry
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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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![Q4 Which statement below about Snl reactions is incorrect?
(A) SNl reactions are stepwise and have intermediates.
(B) The slow step in a Snl reaction is formation of the carbocation intermediate.
(C) SNl reactions have first order kinetics which means only the alkyl halide is
involved in the rate limiting step.
(D) The products of a Syl reaction will be a pair of enantiomers.
(E) An aprotic solvent is best for Snl reactions as they tend to help stabilize
carbocation intermediates.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F11c8f7c5-f059-488e-969e-657a977c9699%2Fb46a9e06-e283-4323-8302-636af71ae572%2Fkycbmo_processed.jpeg&w=3840&q=75)
Transcribed Image Text:Q4 Which statement below about Snl reactions is incorrect?
(A) SNl reactions are stepwise and have intermediates.
(B) The slow step in a Snl reaction is formation of the carbocation intermediate.
(C) SNl reactions have first order kinetics which means only the alkyl halide is
involved in the rate limiting step.
(D) The products of a Syl reaction will be a pair of enantiomers.
(E) An aprotic solvent is best for Snl reactions as they tend to help stabilize
carbocation intermediates.
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