Homework Help is Here – Start Your Trial Now!
Science
Chemistry
I I I I I I 1. NaOCH₂C H3 2. C6H5CH₂I (1 equiv) Ph Select to Draw H3O+ heat Select to Draw × × Ρήτ

I I I I I I 1. NaOCH₂C H3 2. C6H5CH₂I (1 equiv) Ph Select to Draw H3O+ heat Select to Draw × × Ρήτ

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

#37 help 

The image outlines a multi-step organic reaction. Here is the transcription: ### Reaction Overview 1. **Starting Compound:** - The structure shown is a compound with a 1,3-dicarbonyl structure, specifically with an ethyl group on one end and a methyl group on the other. 2. **Step 1:** - **Reagents:** - NaOCH₂CH₃ - C₆H₅CH₂I (1 equivalent) - **Intermediate:** - The product formed is a benzylated 1,3-dicarbonyl compound. The benzyl group (Ph or C₆H₅CH₂) is added to the central carbon of the dicarbonyl. 3. **Step 2:** - **Conditions:** - H₃O⁺ - Heat - **Final Product:** - The reaction results in a rearranged carbon skeleton with a phenyl group (Ph) attached to what was initially the central carbon of the dicarbonyl compound. ### Diagram Explanation - **Initial Compound:** Contains two carbonyl groups connected at the central carbon, with ethyl and methyl groups at each end. - **Intermediate Structure:** The central carbon now has an additional benzyl group, indicated as "Ph." - **Final Product:** Shows the resulting carbon chain after heating and acid treatment, now with phenyl group substitution. Each part of the process is indicated by a downward arrow with reagents and conditions specified alongside. The structural changes in the compounds are indicated in dashed boxes labeled "Select to Draw," but these are not finalized in the image.
Transcribed Image Text:The image outlines a multi-step organic reaction. Here is the transcription: ### Reaction Overview 1. **Starting Compound:** - The structure shown is a compound with a 1,3-dicarbonyl structure, specifically with an ethyl group on one end and a methyl group on the other. 2. **Step 1:** - **Reagents:** - NaOCH₂CH₃ - C₆H₅CH₂I (1 equivalent) - **Intermediate:** - The product formed is a benzylated 1,3-dicarbonyl compound. The benzyl group (Ph or C₆H₅CH₂) is added to the central carbon of the dicarbonyl. 3. **Step 2:** - **Conditions:** - H₃O⁺ - Heat - **Final Product:** - The reaction results in a rearranged carbon skeleton with a phenyl group (Ph) attached to what was initially the central carbon of the dicarbonyl compound. ### Diagram Explanation - **Initial Compound:** Contains two carbonyl groups connected at the central carbon, with ethyl and methyl groups at each end. - **Intermediate Structure:** The central carbon now has an additional benzyl group, indicated as "Ph." - **Final Product:** Shows the resulting carbon chain after heating and acid treatment, now with phenyl group substitution. Each part of the process is indicated by a downward arrow with reagents and conditions specified alongside. The structural changes in the compounds are indicated in dashed boxes labeled "Select to Draw," but these are not finalized in the image.
Expert Solution
trending now

Trending now

This is a popular solution!

steps

Step by step

Solved in 4 steps with 4 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Tools in Analytical Chemistry
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