(thiongl chloride) SOCI2 HQ NaOH - H2D - HO. B. C, D, E (similar to problem with making unsummetniel ethers 'via dehydration of dlech bls )

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...
icon
Related questions
icon
Concept explainers
Question

Show correct mechanism  for the starting material to product A with curved arrows. The remaining B,C, D, E, and F  find mechanism or structure.

**Chemical Reaction Pathways and Mechanisms**

This image depicts a series of chemical reactions involving an aromatic alcohol. Here are the details:

1. **Starting Material**: An aromatic alcohol with the formula where the hydroxyl group (-OH) is attached to a benzene ring.

2. **Reaction with Thionyl Chloride (SOCl₂)**:
   - The reaction shows the conversion of the alcohol to a chlorinated compound (F) using thionyl chloride (SOCl₂).
   - This typically involves the substitution of the hydroxyl group with a chloride ion.

3. **Reaction Pathways**:
   - **Pathway A**: The product from an unspecified reaction involving protonation (H^+) is shown leading to a product labeled as A.
   - **Pathway B**: The same starting material undergoes a reaction with sodium hydroxide (NaOH) producing a compound labeled as B.

4. **Elimination and Formation of Ether**:
   - A dehydration reaction (-H₂O) involving an ether intermediate is indicated. This leads to the formation of products labeled as C, D, and E.
   - The note states these reactions are "similar to the problem with making unsymmetrical ethers via dehydration of alcohols.”

**Note**: The diagram indicates missing reagents or steps needed to complete the pathways for compounds A, B, C, D, and E. Further elucidation may rely on understanding the mechanism by which alcohols are converted to halides, and how ethers can be formed via dehydration.
Transcribed Image Text:**Chemical Reaction Pathways and Mechanisms** This image depicts a series of chemical reactions involving an aromatic alcohol. Here are the details: 1. **Starting Material**: An aromatic alcohol with the formula where the hydroxyl group (-OH) is attached to a benzene ring. 2. **Reaction with Thionyl Chloride (SOCl₂)**: - The reaction shows the conversion of the alcohol to a chlorinated compound (F) using thionyl chloride (SOCl₂). - This typically involves the substitution of the hydroxyl group with a chloride ion. 3. **Reaction Pathways**: - **Pathway A**: The product from an unspecified reaction involving protonation (H^+) is shown leading to a product labeled as A. - **Pathway B**: The same starting material undergoes a reaction with sodium hydroxide (NaOH) producing a compound labeled as B. 4. **Elimination and Formation of Ether**: - A dehydration reaction (-H₂O) involving an ether intermediate is indicated. This leads to the formation of products labeled as C, D, and E. - The note states these reactions are "similar to the problem with making unsymmetrical ethers via dehydration of alcohols.” **Note**: The diagram indicates missing reagents or steps needed to complete the pathways for compounds A, B, C, D, and E. Further elucidation may rely on understanding the mechanism by which alcohols are converted to halides, and how ethers can be formed via dehydration.
Expert Solution
Step 1

Chemistry homework question answer, step 1, image 1

steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Lipids
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