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4.46 How would you prepare cis-but-2-ene starting from propyne, an alkyl halide, and any other reagents needed? (This problem can't be worked in a single step. You’ll have to carry out more than one reaction.)

4.46 How would you prepare cis-but-2-ene starting from propyne, an alkyl halide, and any other reagents needed? (This problem can't be worked in a single step. You’ll have to carry out more than one reaction.)

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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Can you help me answer and explain 4.46

4.46 How would you prepare cis-but-2-ene starting from propyne, an alkyl halide, and any other reagents needed? (This problem can't be worked in a single step. You'll have to carry out more than one reaction.) 4.47 Using but-1-yne as the only organic starting material, along with any inorganic reagents needed, how would you synthesize the following com- pounds? (More than one step may be needed.) (a) Butane (c) 2-Bromobutane (b) 1,1,2,2-Tetrachlorobutane (d) Butan-2-one (CH3CH2COCH3) Activate Wine
Transcribed Image Text:4.46 How would you prepare cis-but-2-ene starting from propyne, an alkyl halide, and any other reagents needed? (This problem can't be worked in a single step. You'll have to carry out more than one reaction.) 4.47 Using but-1-yne as the only organic starting material, along with any inorganic reagents needed, how would you synthesize the following com- pounds? (More than one step may be needed.) (a) Butane (c) 2-Bromobutane (b) 1,1,2,2-Tetrachlorobutane (d) Butan-2-one (CH3CH2COCH3) Activate Wine
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