Question: Show how you would use the acetoacetic ester synthesis to make the following compounds. (a) (b) (c) CH-CHC CH CHCH3 CH3

Show how you would use the acetoacetic ester synthesis to make the following compounds.
(a)

Show how you would use the acetoacetic ester synthesis to

(b)

Show how you would use the acetoacetic ester synthesis to

(c)

Show how you would use the acetoacetic ester synthesis to

CH-CHC CH CHCH3 CH3

Step by Step Solution

★★★★★

3.32 Rating (158 Votes )

There are 3 Steps involved in it

1 Expert Approved Answer
Step: 1 Unlock

In the products the wavy lines indicate the bonds that must be made by alkylation before hydro... View full answer

blur-text-image
Question Has Been Solved by an Expert!

Get step-by-step solutions from verified subject matter experts

Step: 2 Unlock
Step: 3 Unlock

Document Format (1 attachment)

Word file Icon

893-C-O-O-C (1968).docx

120 KBs Word File

Students Have Also Explored These Related Organic Chemistry Questions!

Q:

What products would you expect from the reaction of ethylmagnesium bromide (CH3 CH2MgBr) with each of the following reagents? (a) H2O (b) D2O (c) (d) (e) (f) (g) then H O "H Ph" PhPh, then NH4CI, HO...

Q:

Show how you would use the acetoacetic ester synthesis to prepare (a) 3-propyl-2- hexanone (b) 4-phenyl-2-butanone.

Q:

Show how you would use the Friedel-Crafts acylation, Clemmensen reduction, and or Gatterman-Koch synthesis to prepare the following compounds: (a) (b) (c) (d) p-methoxybenzaldehyde (e)...

Q:

Show how you would use the Robinson annulation to synthesize the following compounds. (a) (b) (c) H,C Ph CH3

Q:

How could you use a malonic ester synthesis to prepare the following compounds? Show allsteps. (b) CH3CH2CH2CHC CH (c) CHCH2C CHCHCH-CH,C C

Q:

(a) Although the following compound is a substituted acetone derivative, it cannot be made by the acetoacetic ester synthesis. Explain why (two reasons). (b) The use of LDA to make enolate ions...

Q:

(a) Explain why the following substituted acetic acid cannot be formed by the malonic ester synthesis. (b) Sections 22-2B and 22-3 showed the use of lithium diisopropylamide (LDA) to deprotonate a...

Q:

Tom Thumbs was asked to prepare the following compounds from the given starting materials. The reagents he chose to use for each synthesis are shown. a. Which of his syntheses were successful? b....

Q:

Please make a (1)practice exam with the blank exam that I was given and provide a (2)key. On the key show the steps on you arrive at the answer concisely. Additionally, make a (3) 5" x 8" notecard...

Q:

Case Study 2 Taxol : An Example of " Fast-Track" Drug Development Introduction following the signing of a cooperative research and development agreement (CWA) between the National Cancer Institute...

Q:

In the following acid-base reactions, 1. Determine which species are acting as electrophiles (acids) and which are acting as nucleophiles (bases). 2. Use the curved-arrow formalism to show the...

Q:

An industrial engineer has designed a new workstation layout that she claims will increase production efficiency. For a sample of 8 workers using the new workstation layout, the average number of...

Q:

Refer to the information given in Problems P12-23 and P12-26 for Alamo and its subsidiary, Western Ranching. Assume that the U.S. dollar is the functional currency and that Alamo uses the fully...

Q:

Question 4 3 ( 1 point ) If you have maximized your RRSP contributions, have positive cash flow and wish to maximize the transfer of wealth to your beneficiaries, which would be the most efficient...

Q:

Use Solver to create a Sensitivity Report for question 16 at the end of Chapter 3, and answer the following questions: a. Is the solution degenerate? b. Explain the value of the shadow price...

Q:

Refer to the financial statements of Campbell Soup Company in Appendix A. Required: a. Determine the net change in long-term debt during Year 11. b. Analyze and discuss the relative mix of debt...

Q:

Use Solver to create a Sensitivity Report for question 35 at the end of Chapter 3 and answer the following questions. a. Is the solution degenerate? b. Is the solution unique? c. How much can the...

Q:

Use Solver to create a Sensitivity Report for question 14 at the end of Chapter 3, and answer the following questions: a. Is the solution degenerate? b. Is the solution unique? c. Suppose the profit...

Q:

Read the "Boeing" case study at the end of chapter 5 in the textbook. Create a PowerPoint presentation of 10-15 slides (including title and reference slides) that teaches one or more of the...

Q:

Calculate the mean, the variance, and the standard deviation of the following discrete probability distribution. x 23 17 9 3 P (X = x) 0.50 0.25 0.15 0.10 Applications

Q:

Synthesize each compound starting from cyclopentanone. (a) (b)

Q:

Provide a mechanism for the following reaction. NaOH H20

Q:

Predict the products of the following reactions. (a) (b) (c) (d) (1) NaOEt, EtOH (3) H2O (1) LDA (1) NaOEt, EtOH (2) H O (3) NaOH (4) CH,CH Br (1) NaOEt, EtOH 0 (3) HO

Q:

Find the pdf of.. [15 pt] Let X have the pdf P(x) = TER. *(1+x2 Find the pdf of Y = X2

Q:

question 27 What is the right sequence for a pecking order? Order the sequence that a firm uses according to the Pecking Order Hypothesis. New common stock Accruals and accounts payable Retained...

Q:

Give an example of a multiple regression with two dichotomous independent variables and a continuous dependent variable. Use your example to explain the concept of multi-colinearity.