10) Which of the following compounds will react most rapidly with HCl? A) 5-methyl-1-hexene B) 4-methyl-1-hexene C) (E)-5-methyl-2-hexene D) (E)-2-methyl-3-hexene E) 2-methyl-2-hexene

Organic Chemistry
8th Edition
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Chapter20: Dienes, Conjugated Systems, And Pericyclic Reactions
Section: Chapter Questions
Problem 20.48P
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10) Which of the following compounds will react most rapidly with HC1?
A) 5-methyl-1-hexene
B) 4-methyl-1-hexene
C) (E)-5-methyl-2-hexene
D) (E)-2-methyl-3-hexene
E) 2-methyl-2-hexene
11) Based on the relative stabilities of the intermediates involved, explain the basis for Markovnikov's rule in
the addition of hydrogen halides to alkenes.
8) Identify the most stable carbocation.
A)
B)
CH₂CH₂
+
CHCH3
CH₂CH3
+
D)
CH₂CH3
E)
CH₂CH3
Ⓒ
Transcribed Image Text:10) Which of the following compounds will react most rapidly with HC1? A) 5-methyl-1-hexene B) 4-methyl-1-hexene C) (E)-5-methyl-2-hexene D) (E)-2-methyl-3-hexene E) 2-methyl-2-hexene 11) Based on the relative stabilities of the intermediates involved, explain the basis for Markovnikov's rule in the addition of hydrogen halides to alkenes. 8) Identify the most stable carbocation. A) B) CH₂CH₂ + CHCH3 CH₂CH3 + D) CH₂CH3 E) CH₂CH3 Ⓒ
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