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I. Synthesize the corresponding alkyne from the given alkene. Show the steps (no need for the mechanism like transfer of electrons- just the arrowed steps) and the reagents needed in the steps CH3 -CH-CH=CH, CH;

I. Synthesize the corresponding alkyne from the given alkene. Show the steps (no need for the mechanism like transfer of electrons- just the arrowed steps) and the reagents needed in the steps CH3 -CH-CH=CH, CH;

Chemistry
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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1. Synthesize the corresponding alkyne from the given alkene. Show the steps (no need for the mechanism like transfer of electrons- just the arrowed steps) and the reagents needed in the steps CH3 -CH-CH=CH₂ CH3 II. Subject the resulting alkyne above to the following reactions (show also the steps and the reagents needed in the steps): a. hydration with mercury as catalyst b. oxidation with potassium permanganate c. hydrohalogenation with HCI (only one HCI is given) d. hydration with borane e. halogenation with bromine (2 molecules of bromine are given) f. hydrogenation with Lindlar catalyst g. hydrogenation with Li/NH3 h. hydrogenation with Pt/C III. If the above alkyne product in I. is subjected to acetylide formation followed by nucleophilic substitution by a primary alkyl halide, show how the following product is formed. CH3 CH3 CH3 -CH-C CH3- C-CH₂-CH-CH- CH3
Transcribed Image Text:1. Synthesize the corresponding alkyne from the given alkene. Show the steps (no need for the mechanism like transfer of electrons- just the arrowed steps) and the reagents needed in the steps CH3 -CH-CH=CH₂ CH3 II. Subject the resulting alkyne above to the following reactions (show also the steps and the reagents needed in the steps): a. hydration with mercury as catalyst b. oxidation with potassium permanganate c. hydrohalogenation with HCI (only one HCI is given) d. hydration with borane e. halogenation with bromine (2 molecules of bromine are given) f. hydrogenation with Lindlar catalyst g. hydrogenation with Li/NH3 h. hydrogenation with Pt/C III. If the above alkyne product in I. is subjected to acetylide formation followed by nucleophilic substitution by a primary alkyl halide, show how the following product is formed. CH3 CH3 CH3 -CH-C CH3- C-CH₂-CH-CH- CH3
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