(a)
Interpretation:
The method of synthesis of given compound has to be stated with the help of acetoacetic ester synthesis.
Concept introduction:
The final products of acetoacetic ester synthesis are
(b)
Interpretation:
The method of synthesis of given compound is to be stated with the help of acetoacetic ester synthesis.
Concept introduction:
The final products of acetoacetic ester synthesis are ketones, specially substituted derivatives of acetone. In acetoacetic ester synthesis, substituents are added to the enolate ion of acetoacetic ester. Then, hydrolysis takes place followed by decarboxylation to give alkylated derivatives of acetone.
(c)
Interpretation:
The method of synthesis of given compound is to be stated with the help of acetoacetic ester synthesis.
Concept introduction:
The final products of acetoacetic ester synthesis are ketones, specially substituted derivatives of acetone. In acetoacetic ester synthesis, substituents are added to the enolate ion of acetoacetic ester. Then, hydrolysis takes place followed by decarboxylation to give alkylated derivatives of acetone.
Want to see the full answer?
Check out a sample textbook solutionChapter 22 Solutions
Organic Chemistry (9th Edition)
- A DEPT NMR spectrum is shown for a molecule with the molecular formula of C5H12O. Draw the structure that best fits this data. 200 180 160 140 120 100 一盆 00 40 8- 20 ppm 0 Qarrow_forwardDon't used hand raitingarrow_forwardShown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H. H. +N=C H H H Cl: Click and drag to start drawing a structure. : ? g B S olo Ar B Karrow_forward
- Don't used hand raitingarrow_forwardS Shown below is the major resonance structure for a molecule. Draw the second best resonance structure of the molecule. Include all non-zero formal charges. H H = HIN: H C. :0 H /\ H H Click and drag to start drawing a structure. ×arrow_forwardPlease help me figure out these calculation and what should be plotted. These are notes for my chemistry class.arrow_forward
- Nonearrow_forwardNonearrow_forwardPart II. two unbranched ketone have molecular formulla (C8H100). El-ms showed that both of them have a molecular ion peak at m/2 =128. However ketone (A) has a fragment peak at m/2 = 99 and 72 while ketone (B) snowed a fragment peak at m/2 = 113 and 58. 9) Propose the most plausible structures for both ketones b) Explain how you arrived at your conclusion by drawing the Structures of the distinguishing fragments for each ketone, including their fragmentation mechanisms.arrow_forward
- Organic ChemistryChemistryISBN:9781305580350Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. FootePublisher:Cengage LearningOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning