Describe the synthesis preparation of Aldol condensation products
Carbonyl compounds in which – H atoms are present, undergoes to self condensation in presence of dilute alkali or dilute base. The product formed contains both –OH and >C = O group. So, the compound is called Aldol or Ketol which on –elimination gives unsaturated carbonyl compound. The complete reaction is called ‘Aldol – Condensation’. Formaldehyde cannot show aldol condensation due to absence of –Hydrogen atoms.
In aldol condensation, if we take two different type of aldehyde or ketone then it is called mixed aldol condensation.
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Postlab Assignment for Minilab 34 “Preparation of Aldol Condensation Products” 1. Explain why benzaldehyde is expected to be the most reactive aldehyde among the three aldehydes used in this experiment. (used benzaldehyde, 4-methylbenzaldehyde, and 4-methoxybenzaldehyde) 2. What is the role of aqueous NaOH used in the experiment you carried out? 3. How would you change the procedures in this experiment if you wished to synthesize benzalacetophenone (C6H5CH=CHCOC6H5). Just indicate the two main organic starting materials. 4. Write a mechanism for...
preparation of dibenzalacetone by using an aldol condensation. full mechanism explained full detail
Describe aldol condensation reactions generally and mixed aldol reactions specifically.
Preparation of and alpha, beta-unsaturated ketone via Michael and Aldol Condensation: 6-ethoxycarbonyl-3,5-diphenyl-2-cyclohexanone.Draw a mechanism for each of the three steps in the preparation of 6-ethoxycarbonyl-3,5-diphenyl-2-cyclohexenone. You may assume that NaOH functions as a base andethanol serves as a proton source
The Aldol condensation: Synthesis of dibenzalacetone I need help with question 4 and the second part of 5 please.
4. Draw all of the possible Aldol products (B-hydroxycarbonyl) for the following reaction below. Condensation products are not necessary. (3 points) NaOH Aldol Products
Which reactants would react using the aldol condensation to form these products? Which reactants would react using the aldol condensation to form these products?
4. Draw all of the possible Aldol products (B-hydroxycarbonyl) for the following reaction below. Condensation products are not necessary. (3 points) NaOH Aldol Products .Ph Me H2O Ph Ме
What are the possible aldol condensation products and structures of the products from this list of ketones and aldehydes? Possible ketones: acetone, cyclopentanone, cyclohexanone, and 4-methylcyclohexanone, Possible aldehydes: benzaldehyde, 4-methylbenzaldehyde, 4-anisaldehyde, and trans cinnamaldehyde.
Draw the structures of the aldol addition and condensation products of pentanal. Draw only one final condensation product.