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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