### Transcription for Educational Website---**Topic: Synthesis of Substituted Alkynes****Question:** 9.6 What terminal alkyne and alkyl halide react to give the following compound?**Reaction Overview:**- **Reactant:** A sodium amide (NaNH₂) reagent is used to facilitate the reaction.- **Product:** The target compound depicted is a branched alkyne featuring a triple bond connected to an ethyl group and an isopropyl group.**Note:** The hint suggests observing the nature of the alkyne substituents—in this case, indicating that one alkyne substituent is primary and the other is secondary.### Diagram Explanation:The diagram consists of:1. **Chemical Arrow:** - Indicates the direction of the reaction from left to right, with NaNH₂ above the arrow.2. **Structural Formula of Product:** - Features a carbon chain with a triple bond (alkyne). - On one side, an ethyl group is attached. - On the other, an isopropyl group is connected.**Hint Explanation:**The hint emphasizes the structural nature of the substituents around the alkyne:- **Primary Substituent:** Contains a carbon attached to only one other carbon.- **Secondary Substituent:** Contains a carbon attached to two other carbons.This information is critical for determining the initial reactants required for the synthesis of the compound.---

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Answered: 9.6 What terminal alkyne and alkyl…

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9.6 What terminal alkyne and alkyl halide react to give the following compound? NaNH,

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

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Concept explainers

Organomagnesium compounds

The interaction of alkyl halide with Mg metal in a suitable ether solvent is the common method for the synthesis of the Grignard reagent.

Hydrolysis Grignard Reactions and Reduction

Organomagnesium halides are Grignard reagents. Francois Auguste Victor Grignard, a French chemist who received the Nobel Prize in Chemistry in 1912, created these highly useful reagents.

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