show how you would make this compound... 2. Show how you would make this compound by...
1. a) Draw the structure of an enol of this compound. If no enol is possible, write "none possible". b) How many acidic hydrogens (pka <22) does this compound have? c) Can this compound react with I/KOH in the haloform reaction? If so, give the products. If not, state why not. 2. Show how you would make this compound by a malonic ester synthesis or an acetoacetic acid synthesis. hexanoic acid 3. Write in the products of these reactions: NaOCH2CH3...
11) Show how to synthesize 2-Methylhexanoic acid using the Malonic Ester Synthesis. Start with Diethyl propanedioate (C7H1204)
show stepwise how you would prepare the following compounds
from the provided starting material and any other organic or
inorganic compound.
in order to have full credit you mush show all the reactions
conditions and the structure of your oroducts in each
transformation
(30 points) Show stepwise how would you prepare the following compounds from the provided starting material and any other organic or inorganic compound. In order to have full credit you must show all the reaction conditions and...
This is for Organic II. Thank you!
4) Devise a synthesis for the following compound V using a) a Claisen condensation, and b) a Malonic or acetoacetic ester synthesis.
DQuestion 1 1 pts See Figure 11-1. To make Compound 1 using the malonic ester synthesis, you would react malonic ester with 1. base and 2. Select ] 3. base and 4 I Select l I Select ] D Question 2 1 pts See Figure 11-1. To make Compound 2 using the malonic ester synthesis, you would react malonic ester with 1. base and 2. Select 3. base and 4. I Select ]
7. What two molecules could be used to make the following molecules using crossed aldol reaction. O ook OH 8a. There are 4 alpha-carbons in this molecule. Which alpha carbon(s) is/are the most reactive? What is the product if NaOH and heat are used? 8b. What is the scientist name whom the above reaction is named after? 9. Why does the base (used to proton transfer) need match the initial reactant in the Claisen Condensation? 10. Malonic ester synthesis questions...
7. What two molecules could be used to make the following molecules using crossed aldol reaction. ook OH 8a. There are 4 alpha-carbons in this molecule. Which alpha carbon(s) is/are the most reactive? What is the product if NaOH and heat are used? a 8b. What is the scientist name whom the above reaction is named after? 9. Why does the base (used to proton transfer) need match the initial reactant in the Claisen Condensation? 10. Malonic ester synthesis questions...
7. What two molecules could be used to make the following molecules using crossed aldol reaction. OH 8a. There are 4 alpha-carbons in this molecule. Which alpha carbon(s) is/are the most reactive? What is the product if NaOH and heat are used? 8b. What is the scientist name whom the above reaction is named after? 9. Why does the base (used to proton transfer) need match the initial reactant in the Claisen Condensation? 10. Malonic ester synthesis questions - Show...
The Malonic Acid synthesis is similar to the Acetoacetic Ester synthesis It uses diethyl malonate as the main starting material Draw the structure of diethyl malonate (malonic ester) Diethyl malonate can be hydrolyzed back to malonic acid and if heat is applied after the hydrolysis, will decarboxylate. Draw the mechanism for this transformation starting with malonic acid. Indicate the new C-C bonds in each molecule and then provide the organohalides which were used to synthesize each compound using the malonic...
6. Using either malonic ester synthesis or acetoacetic ester synthesis, outline a reaction scheme in each case to show how you will synthesize compounds A and B below. [Show all steps with structure of all intermediates and necessary reagents). A. 3-butyl-2-tetradecanone B. 2-propylpentadecanoic acid