Why is there more inversion than retention of configuration in SN1 reaction? A. The carbocation intermediate is not a planar structure. B. Approach of the nucleophile is hindered by the leaving group. C. SN1 reaction is reversible. D. Nucleophile forms a bond before the leaving group leaves. E. Reaction can never be 100% SN1, there is always some SN2 happening. Which alcohol below would undergo acid-catalyzed dehydration most readily? CH,OH OH НО А. В. C. D. НО Е. ÓH

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter14: Elimination
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Why is there more inversion than retention of configuration in SN1 reaction?
A. The carbocation intermediate is not a planar structure.
B. Approach of the nucleophile is hindered by the leaving group.
C. SN1 reaction is reversible.
D. Nucleophile forms a bond before the leaving group leaves.
E. Reaction can never be 100% SN1, there is always some SN2 happening.
Which alcohol below would undergo acid-catalyzed dehydration most readily?
CH,OH
OH
НО
А.
В.
C.
D.
НО
Е.
ÓH
Transcribed Image Text:Why is there more inversion than retention of configuration in SN1 reaction? A. The carbocation intermediate is not a planar structure. B. Approach of the nucleophile is hindered by the leaving group. C. SN1 reaction is reversible. D. Nucleophile forms a bond before the leaving group leaves. E. Reaction can never be 100% SN1, there is always some SN2 happening. Which alcohol below would undergo acid-catalyzed dehydration most readily? CH,OH OH НО А. В. C. D. НО Е. ÓH
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