[Review Topics] [References] Devise a synthesis of (E)-3-octene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials HCECH 1 Reagents HCEC-CH₂ 2 a NaNH NH(0) b NaOH/H₂O c iodomethane Starting material Reagent for step 1 Reagent for step 2 Reagent for step 3 Submit Answer HC=C–CH,CH, 3 diodoethane e 1-bromopropane f 2-bromopropane Retry Entire Group HCEC-CH₂CH₂CH₂CH₂ 4 g 1-bromo-3-methylbutane h t-butyl bromide i H₂/Pd on carbon CH₂ HCEC-C-CH₂ H 5 9 more group attempts remaining KHINH(D) CH₂ HC=C-C-CH₂ CH₂ jH₂! Lindlar catalyst I Na/NH₂(0 6 Previous Email Instructor Next Save and Exit

[Review Topics] [References] Devise a synthesis of (E)-3-octene using one of the starting materials and any of the reagents below using the fewest steps possible. If you need fewer than the 3 steps allowed, enter "none" for reagents in the remaining unused steps. Starting materials HCECH 1 Reagents HCEC-CH₂ 2 a NaNH NH(0) b NaOH/H₂O c iodomethane Starting material Reagent for step 1 Reagent for step 2 Reagent for step 3 Submit Answer HC=C–CH,CH, 3 diodoethane e 1-bromopropane f 2-bromopropane Retry Entire Group HCEC-CH₂CH₂CH₂CH₂ 4 g 1-bromo-3-methylbutane h t-butyl bromide i H₂/Pd on carbon CH₂ HCEC-C-CH₂ H 5 9 more group attempts remaining KHINH(D) CH₂ HC=C-C-CH₂ CH₂ jH₂! Lindlar catalyst I Na/NH₂(0 6 Previous Email Instructor Next Save and Exit

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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