Show the mechanisms **Practice:** Draw the product for the following reactionsa. \[ \text{H--C}\equiv\text{C--H} \xrightarrow{[1] \text{NaH}} \quad \text{(arrow pointing to the right)} \quad \xrightarrow{[2] \text{CH}_3CHClCH_3} \]**Explanation:**- Reactant: Acetylene (\(\text{H--C}\equiv\text{C--H}\))- Reagents: 1. Sodium hydride (NaH) 2. 2-Chloropropane (\(\text{CH}_3CHClCH_3\))To obtain the final product, students are expected to understand the steps:1. The acetylene (\(\text{H--C}\equiv\text{C--H}\)) reacts with sodium hydride (NaH). Sodium hydride deprotonates the acetylene, creating an acetylide anion (\(\text{H--C}\equiv\text{C}^- \text{Na}^+ \)).2. The acetylide anion then reacts with 2-chloropropane (\(\text{CH}_3CHClCH_3\)), where a nucleophilic substitution occurs, resulting in the addition of the substituted propyl group to the acetylene.Students are expected to draw the complete structure of the final organic product synthesized through these two steps.Note: The actual drawing of the resulting product is not included in this transcription and should be illustrated as per the instructor's guidance or additional problem context.

When ethyne is treated with sodium hydride and subsequently with 1-chloro -2-methylpropane then…

Answered: Practice: Draw the product for the…

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Chemistry

Practice: Draw the product for the following reactions (1) NaH a. H-C=C-H (2] CI

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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