НО, ОН -ОН Но, HO

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
Question

Draw the complete electron pushing mechanism that is enzyme catalyzed. 

### Explanation of Chemical Reaction

This image illustrates a chemical reaction involving a structural transformation of a compound. 

#### Reactant: 
- On the left side is the compound Hydroxyquinone, also known as 1,4-benzoquinone or para-benzoquinone. It has a six-membered aromatic ring with two hydroxyl groups (OH) positioned at the 1,4-positions (para position) and a carbonyl group (C=O) at the top of the benzene ring.

#### Product:
- On the right side is Hydroquinone, also known as benzene-1,4-diol. It maintains the same six-membered aromatic ring structure, but the carbonyl group has been reduced to a hydroxyl group (OH), resulting in a total of three hydroxyl groups in the structure, one each at the 1, 4, and new position previously occupied by the carbonyl.

#### Reaction Arrow:
- The arrow between the two structures indicates a chemical reaction or transformation from Hydroxyquinone to Hydroquinone. Specifically, this transformation involves the reduction of the carbonyl group to a hydroxyl group.

This type of reaction is significant in the study of organic chemistry and demonstrates the conversion processes between quinones and their reduced forms.
Transcribed Image Text:### Explanation of Chemical Reaction This image illustrates a chemical reaction involving a structural transformation of a compound. #### Reactant: - On the left side is the compound Hydroxyquinone, also known as 1,4-benzoquinone or para-benzoquinone. It has a six-membered aromatic ring with two hydroxyl groups (OH) positioned at the 1,4-positions (para position) and a carbonyl group (C=O) at the top of the benzene ring. #### Product: - On the right side is Hydroquinone, also known as benzene-1,4-diol. It maintains the same six-membered aromatic ring structure, but the carbonyl group has been reduced to a hydroxyl group (OH), resulting in a total of three hydroxyl groups in the structure, one each at the 1, 4, and new position previously occupied by the carbonyl. #### Reaction Arrow: - The arrow between the two structures indicates a chemical reaction or transformation from Hydroxyquinone to Hydroquinone. Specifically, this transformation involves the reduction of the carbonyl group to a hydroxyl group. This type of reaction is significant in the study of organic chemistry and demonstrates the conversion processes between quinones and their reduced forms.
Expert Solution
steps

Step by step

Solved in 2 steps with 2 images

Blurred answer
Knowledge Booster
Acid-Base Titrations
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