Write the steps in the mechanism of the base catalyzed condensation of the following compounds:
A. 2CH3CH2C(O)H
B.CH3C(O)CH3+2C6H5C(O)H
I think this is an aldol reaction; see the mechanism section at the link below.
Source(s):http://en.wikipedia.org/wiki/Aldol_conde...
An aldol condensation is an organic reaction in which an enol or an enolate ion reacts with a carbonyl compound to form a ?-hydroxyaldehyde or ?-hydroxyketone, followed by a dehydration to give a conjugated enone.
Aldol condensations are important in organic synthesis, providing a good way to form carbon
Write the steps in the mechanism of the base catalyzed condensation of the following compounds: A....
Show the mechanism for a base-catalyzed aldol condensation of the reaction. Use any appropriate base. Show the mechanism for an acid-catalyzed aldol concentration of the reaction. use any apporproate acid. 2. Draw and name the compound resulting from the aldol condensation of vanillin with creatinine. сн, NH но- 160°C NH CH Vanillin Creatinine 2. Draw and name the compound resulting from the aldol condensation of vanillin with creatinine. сн, но- NH 160 C NH сH, Vanillin Creatinine
Predict major product (WITH MECHANISM) of the base-catalyzed aldol condensation with dehydration of: methyl phenyl ketone + 2,2-dimethylpropanal
Please show all steps . Thank you Provide a detailed, wise mechanism for the acid-catalyzed condensation reaction between step benzaldehyde and methylamine
show a mechanism of formatiin if the following enol under base catalyzed conditions We were unable to transcribe this imageShow a mechanism of formation of the following enol under base-catalyzed conditions: For the mechanism, draw the curved arrows as needed. Include lone pairs and charges in your answer. Do not draw out any hydrogen explicitly in your products. Do n use abbreviations such as Me or Ph. Step 1 0 Get help answering Molecular Drawing question Draw step 1 of...
Define (reaction only) the base catalyzed cross-aldol condensation reaction between excess benzaldehyde and propanaldehyde (No mechanism needed)!
1. Draw the complete curved-arrow mechanism for the base-catalyzed aldol condensation to form dehydrorheosmin (or dehydrozingerone) from acetone and 4-hydroxybenzaldehyde (or vanillin). (2 points)
Base-catalyzed crossed aldol condensation followed by the oxa-michael addition reaction mechanism for the reaction above! Thank you!! 20 10 F4 FOF2 DOO FS F9 0 A 6 7 8L 0 diiso propylamine (DIPA) EtoH + HP
Unit 3 Homework Assignment Name 1. The first two steps in the base-catalyzed condensation of acetaldehyde would be described as: a. attack of Off on the carbonyl carbon atom, then loss of water b. attack of OH on the carbonyl carbon atom, then the resultant anion attacks the carbon atom on a second molecule of acetaldehyde. carbonyl bstracts an alpha-hydrogen atom, then the resultant anion attacks the carbonyl carbon atom on a second molecule of acetaldehyde. d. Oir abstracts the...
Write a curved arrow mechanism for the acid catalyzed Fischer esterification of benzoic acid in CH3O*H (that is 0-18 labeled methanol). Show all steps, lone pair of electrons, charges and labeled O atoms through the mechanism.
can someone do 1-3? Pechmann Condensation 1. Propose a mechanism for the acid-catalyzed Pechmann condensation of resorcinol and ethyl acetoacetate. Identify the transesterification, electrophilic aromatic substitution and dehydration steps. 2. Would you expect 1,3,5-trihydroxybenzene (phloroglucinol) to react more quickly or more slowly than resorcinol? Why or why not? 3. Consider and discuss the greenness of Pechmann Reaction. 4. Discuss and assign the peaks (chemical shift, splitting pattern, etc) in the 1H NMR and IR spectra of your product INDO,