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: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter13: Substitution
Section: Chapter Questions
Problem 8CTQ
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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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