Homework Help is Here – Start Your Trial Now!
Science
Chemistry
Draw the starting alkyne that would lead to the following two products under these conditions. Select to Draw 1. KMNO4, OH- (warm) 2. НзО* HO. Но

Draw the starting alkyne that would lead to the following two products under these conditions. Select to Draw 1. KMNO4, OH- (warm) 2. НзО* HO. Но

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...
See similar textbooks
icon
Related questions
Question
100%
**Title: Organic Chemistry Reaction: Identifying Alkynes** **Objective:** Draw the starting alkyne that would lead to the following two products under these specified reaction conditions. --- **Instructions:** 1. **Reaction Conditions:** - Use the following reagents in the reaction: 1. **KMnO₄, OH⁻** (warm conditions) 2. **H₃O⁺** 2. **Expected Chemical Transformation:** - The reaction involves oxidation of an alkyne to yield two carboxylic acid products. 3. **Chemical Products Formed:** - The products of the reaction are two carboxylic acids. The structure of the products is shown in the diagram: - **Product 1:** A six-membered cyclic compound with a carboxylic acid (–COOH) and an alcohol (–OH) group attached to adjacent carbons. - **Product 2:** A linear chain with a carboxylic acid group (–COOH) and a methyl group (–CH₃). 4. **Challenge:** - Draw the structure of the alkyne that would react under these conditions to yield the mentioned products. Use the "Select to Draw" tool to illustrate. 5. **Diagram Description:** - The illustration involves a process flow where an unspecified alkyne (to be drawn) undergoes reaction steps, leading finally to the depicted carboxylic acid structures. **Discussion:** Understanding this reaction requires knowledge of alkyne oxidation, specifically through oxidative cleavage where KMnO₄ is used to break triple bonds and form carboxylic acids. This understanding will aid in hypothesizing the original alkyne structure needed to obtain the desired products. Remember, mastering these transformations is crucial for organic synthesis and reaction mechanism analysis in advanced chemistry studies!
Transcribed Image Text:**Title: Organic Chemistry Reaction: Identifying Alkynes** **Objective:** Draw the starting alkyne that would lead to the following two products under these specified reaction conditions. --- **Instructions:** 1. **Reaction Conditions:** - Use the following reagents in the reaction: 1. **KMnO₄, OH⁻** (warm conditions) 2. **H₃O⁺** 2. **Expected Chemical Transformation:** - The reaction involves oxidation of an alkyne to yield two carboxylic acid products. 3. **Chemical Products Formed:** - The products of the reaction are two carboxylic acids. The structure of the products is shown in the diagram: - **Product 1:** A six-membered cyclic compound with a carboxylic acid (–COOH) and an alcohol (–OH) group attached to adjacent carbons. - **Product 2:** A linear chain with a carboxylic acid group (–COOH) and a methyl group (–CH₃). 4. **Challenge:** - Draw the structure of the alkyne that would react under these conditions to yield the mentioned products. Use the "Select to Draw" tool to illustrate. 5. **Diagram Description:** - The illustration involves a process flow where an unspecified alkyne (to be drawn) undergoes reaction steps, leading finally to the depicted carboxylic acid structures. **Discussion:** Understanding this reaction requires knowledge of alkyne oxidation, specifically through oxidative cleavage where KMnO₄ is used to break triple bonds and form carboxylic acids. This understanding will aid in hypothesizing the original alkyne structure needed to obtain the desired products. Remember, mastering these transformations is crucial for organic synthesis and reaction mechanism analysis in advanced chemistry studies!
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 2 steps with 1 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Alcohols
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY
SEE MORE TEXTBOOKS