64.Percentage yied of Elimination Product I.CH3CHBRCH₂CH₂CH3 + CH3S/DMSO → II.CH3CHBRCH₂CH₂CH3 + CH3O/CH3OH → 65.Reactivity of the alkylhalide in an E2 Reaction C6H5CH₂CHBRCH₂CH3 C6H5 CH₂CH₂CHBRCH3 66. Reactivity toward the Nucleophile CH3O I. O,N- II. CH₂N- I. II. I. O H 67. Percentage yield of 4,4-dimethyl-1-pentene II. -CHO CH3 CH3-C-CH₂CHBRCH3 CH3 CH3 CH₂-C-CH₂CHBRCH3 CH₂ (CH₂)₂CO-K+ (CH3)3COH CH₂CH₂O-K+ CH₂CH₂OH
64.Percentage yied of Elimination Product I.CH3CHBRCH₂CH₂CH3 + CH3S/DMSO → II.CH3CHBRCH₂CH₂CH3 + CH3O/CH3OH → 65.Reactivity of the alkylhalide in an E2 Reaction C6H5CH₂CHBRCH₂CH3 C6H5 CH₂CH₂CHBRCH3 66. Reactivity toward the Nucleophile CH3O I. O,N- II. CH₂N- I. II. I. O H 67. Percentage yield of 4,4-dimethyl-1-pentene II. -CHO CH3 CH3-C-CH₂CHBRCH3 CH3 CH3 CH₂-C-CH₂CHBRCH3 CH₂ (CH₂)₂CO-K+ (CH3)3COH CH₂CH₂O-K+ CH₂CH₂OH
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Question
![A -if the indicated property/behavior in item I is greater than in item II
B-if the indicated property/behavior in item I is less than in item II.
C- if the indicated property/behavior is equal in item I and item II.
D- if the indicated data is insufficient to make a comparison.](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F2ce0bc1f-fff8-4bfd-b333-45eafe255b44%2F9fc01c52-059f-4408-b925-b6c14fedebbc%2Fx27secd_processed.png&w=3840&q=75)
Transcribed Image Text:A -if the indicated property/behavior in item I is greater than in item II
B-if the indicated property/behavior in item I is less than in item II.
C- if the indicated property/behavior is equal in item I and item II.
D- if the indicated data is insufficient to make a comparison.
![64.Percentage yied of Elimination Product
I.CH3CHBRCH₂CH₂CH3 + CH3S/DMSO →
II.CH3CHBRCH₂CH₂CH3
+ CH3O/CH3OH →
65.Reactivity of the alkylhalide in an E2 Reaction
C6H5CH₂CHBRCH₂CH3
C6H5 CH₂CH₂CHBRCH3
66. Reactivity toward the Nucleophile CH3O
I.
O₂N-
II.
CH₂N-
I.
II.
I.
O
H
67. Percentage yield of 4,4-dimethyl-1-pentene
II.
-CHO
CH3
CH3-C-CH₂CHBRCH3
CH3
CH3
CH₂-C-CH₂CHBRCH3
CH₂
(CH₂)₂CO-K+
(CH3)3COH
CH₂CH₂O-K+
CH₂CH₂OH](/v2/_next/image?url=https%3A%2F%2Fcontent.bartleby.com%2Fqna-images%2Fquestion%2F2ce0bc1f-fff8-4bfd-b333-45eafe255b44%2F9fc01c52-059f-4408-b925-b6c14fedebbc%2Fdj9kxwn_processed.png&w=3840&q=75)
Transcribed Image Text:64.Percentage yied of Elimination Product
I.CH3CHBRCH₂CH₂CH3 + CH3S/DMSO →
II.CH3CHBRCH₂CH₂CH3
+ CH3O/CH3OH →
65.Reactivity of the alkylhalide in an E2 Reaction
C6H5CH₂CHBRCH₂CH3
C6H5 CH₂CH₂CHBRCH3
66. Reactivity toward the Nucleophile CH3O
I.
O₂N-
II.
CH₂N-
I.
II.
I.
O
H
67. Percentage yield of 4,4-dimethyl-1-pentene
II.
-CHO
CH3
CH3-C-CH₂CHBRCH3
CH3
CH3
CH₂-C-CH₂CHBRCH3
CH₂
(CH₂)₂CO-K+
(CH3)3COH
CH₂CH₂O-K+
CH₂CH₂OH
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