Homework Help is Here – Start Your Trial Now!
Science
Chemistry
CH3 CH3 CH2 HÇ CH3 hv + H3C CH3 || CH3 H;C CH3 CH2 CH3

CH3 CH3 CH2 HÇ CH3 hv + H3C CH3 || CH3 H;C CH3 CH2 CH3

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

What is the mechanism?

This image depicts a photochemical reaction, specifically the photoinduced alpha-cleavage (also known as the Norrish Type I reaction) of a carbonyl compound. **Reactant:** - The left side shows a cyclic ketone. The structure is a six-membered ring with a carbonyl group (C=O) and two methyl groups (CH₃) attached to the third and sixth carbon atoms. **Reaction Conditions:** - The reaction is initiated by light (represented by "hν"), indicating the photochemical nature of the process. **Products:** - Two products are formed: 1. The first product is a five-membered ring (cyclopentanone) with a carbonyl group and a vinyl group (CH=CH₂) attached. It also contains a methyl group attached to the second carbon. 2. The second product is another cyclopentenone with a carbonyl group and a vinyl group, but with one methyl group attached to the third carbon. This type of reaction often involves the homolytic cleavage of the bond adjacent to the carbonyl group upon absorption of light, resulting in the generation of radicals and subsequent rearrangement.
Transcribed Image Text:This image depicts a photochemical reaction, specifically the photoinduced alpha-cleavage (also known as the Norrish Type I reaction) of a carbonyl compound. **Reactant:** - The left side shows a cyclic ketone. The structure is a six-membered ring with a carbonyl group (C=O) and two methyl groups (CH₃) attached to the third and sixth carbon atoms. **Reaction Conditions:** - The reaction is initiated by light (represented by "hν"), indicating the photochemical nature of the process. **Products:** - Two products are formed: 1. The first product is a five-membered ring (cyclopentanone) with a carbonyl group and a vinyl group (CH=CH₂) attached. It also contains a methyl group attached to the second carbon. 2. The second product is another cyclopentenone with a carbonyl group and a vinyl group, but with one methyl group attached to the third carbon. This type of reaction often involves the homolytic cleavage of the bond adjacent to the carbonyl group upon absorption of light, resulting in the generation of radicals and subsequent rearrangement.
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
Alkanes and Cycloalkanes
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