Organic Chemistry
Organic Chemistry
11th Edition
ISBN: 9781118133576
Author: T. W. Graham Solomons, Craig Fryhle
Publisher: Wiley, John & Sons, Incorporated
bartleby

Concept explainers

bartleby

Videos

Textbook Question
Book Icon
Chapter 18, Problem 2LGP

Dehydroabietic acid is a natural product isolated from Pinus palustris. It is structurally related to abietic acid, which comes from rosin. The synthesis of dehydroabietic acid (J. Am. Chem. Soc. 1962, 84, 284–292) was accomplished by Gilbert Stork. In the course of this synthesis, Stork discovered his famous enamine reaction.

(a) Write detailed mechanisms for the reactions from 6 to 8 below.

(b) Write detailed mechanisms for all of the reactions from 9 to 11 in Stork’s synthesis of dehydroabietic acid. Note that 11 contains a dithioacetal, which forms similarly to acetals you have already studied (Chapter 16).

Chapter 18, Problem 2LGP, Dehydroabietic acid is a natural product isolated from Pinus palustris. It is structurally related

(Fleming, I., Selected Organic Synthesis, p. 76. Copyright John Wiley & Sons, Limited. Reproduced with permission.)

Blurred answer
Students have asked these similar questions
Propanal and propanone react in a similar way with acidified aqueous potassium cyanide, KCN.  For this reaction to occur reasonably quickly, the pH of the solution should be approximately 4. The reaction of propanal proceeds with acidified potassium cyanide proceeds more rapidly than that of propanone. Referring to the mechanism of the reactions, explain this phenomenon.
Propose a feasible synthesis for diphenylacetylene from bromobenzene. Draw the reaction scheme and briefly describe the reaction.
Draw the chemical structure of a 1,2,3-triazole and showv how it can be synthesized from (b) basic starting materials. Comment on the acidity and basicity of triazoles. Comment on their reactivity towards electrophilic aromatic substitution relative to pyridines and pyrroles.

Chapter 18 Solutions

Organic Chemistry

Knowledge Booster
Background pattern image
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.
Similar questions
SEE MORE QUESTIONS
Recommended textbooks for you
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305080485
    Author:John E. McMurry
    Publisher:Cengage Learning
    Text book image
    Organic Chemistry: A Guided Inquiry
    Chemistry
    ISBN:9780618974122
    Author:Andrei Straumanis
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305080485
Author:John E. McMurry
Publisher:Cengage Learning
Text book image
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
NMR Spectroscopy; Author: Professor Dave Explains;https://www.youtube.com/watch?v=SBir5wUS3Bo;License: Standard YouTube License, CC-BY