**Instruction for Multi-step Synthesis:**Outline a multi-step synthesis for how to synthesize the molecule below from acetylene. Use any other reagents necessary. Steps must be separated with reaction arrows. Your scheme should include intermediate products, all reagents and solvents when necessary.**Starting Material:**- Acetylene (HC≡CH)**Target Molecule:**- 2-Methyl-2-butanol (OH is connected to a tertiary carbon with the molecular structure as shown below) ``` OH | CH / \ H3C C / \ H2 CH3 ```**Schematic Representation:**- The synthesis pathway involves multiple steps indicated by a horizontal arrow labeled "multiple steps" from acetylene to the target molecule.

Acetylene on reaction with sodamide in liquid ammonia form nucleophile (sodium acetanilide) which after reaction with n-propyl bromide produces pent-1-yne. Pent-1-yne after reduction with sodium borohydride gives alcohol.

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Outline a multi-step synthesis for how to synthesisze the molecule below from acetylene. Use any other reagents necessary. Steps must be separated with reaction arrows. Your scheme should include intermediate products, all reagents and solvents when necessary. ОН H2 CH H3C HC CH multiple steps CH3 H2

Outline a multi-step synthesis for how to synthesisze the molecule below from acetylene. Use any other reagents necessary. Steps must be separated with reaction arrows. Your scheme should include intermediate products, all reagents and solvents when necessary. ОН H2 CH H3C HC CH multiple steps CH3 H2

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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