Maxwell presented by Macmillan Learning Draw the structure of the starting material needed to make 2-methylhept-3-yne (or 2-methyl-3-heptyne) using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons. Draw the starting hydrocarbon. Select Draw Rings More Erase H 1) NaNH,, NH3() + NaBr 2) CH;CH,CH,Br
Maxwell presented by Macmillan Learning Draw the structure of the starting material needed to make 2-methylhept-3-yne (or 2-methyl-3-heptyne) using sodium amide in liquid ammonia, followed by 1-bromopropane. The starting hydrocarbon must have no more than five carbons. Draw the starting hydrocarbon. Select Draw Rings More Erase H 1) NaNH,, NH3() + NaBr 2) CH;CH,CH,Br
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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Transcribed Image Text:**Organic Chemistry**
Presented by Macmillan Learning
**Objective:**
Draw the structure of the starting material needed to make 2-methylhept-3-yne (or 2-methyl-3-heptyne) using sodium amide in liquid ammonia, followed by 1-bromopropane.
**Instructions:**
The starting hydrocarbon must have no more than five carbons. Draw the starting hydrocarbon.
**Tools Available:**
- **Select**: Choose parts of the structure.
- **Draw**: Tools for drawing lines and structures, including single, double, and triple bonds.
- **Rings**: Options to add ring structures.
- **More**: Access additional options.
- **Erase**: Remove parts of the structure.
- **C**: Add carbon atoms.
- **H**: Add hydrogen atoms.
- **Undo/Redo**: Navigate through changes.
**Chemical Reaction Steps:**
1. **Reagents**: NaNH₂, NH₃ (l)
2. **Substrate**: 1) CH₃CH₂CH₂Br (1-bromopropane)
**Outcome:**
- A structure of 2-methylhept-3-yne is depicted with an arrow indicating the reaction process leading to the formation of the compound.
- Byproduct: NaBr
This educational content provides a step-by-step guide to understanding and executing organic synthesis to form a specific alkyne compound.
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