What is the balanced chemical equation for this reaction?
Alpha carbon atom of diphenylketone convert enolate in presence of base.
Enolate react with 1,2 diphenylethanesione.
Proton loss from beta carbon atom of diphenylketone (water molecule loss) to form hydroxy intermediate.
Which undergo cyclisation by loss of water molecule from ketone group in 1,2 diphenylethane dione.
Finally form tetraphenyl cyclopentanedione.
Reaction:
What is the balanced chemical equation for this reaction? HE ALDOL REACTION: TETRAPHENYLCYCLOPENTADIENONE Synthetic Chemistry Lab....
What is the product of a diels-alder reaction between 9-anthracenemethan and N-methylmaleimide in water? what is the product's name? Figure 1. The reaction between 9-anthracenemethanol and N-methylmaleimide N-CH3 Н.о -CHs Он он Experimental Instructions N-methylmaleimide is corrosive and should be handled with care. Always wear gloves and eye protection in the laboratory 1. Place 0.065q of finely pulverized 9-anthracenemethanol and 50 mL of water in a 100-mL round-bottomed flask equipped with a magnetic.stir bar. 2. Add 3 molar equivalents of...
Please help answer P1-P4 for this Perkin Reaction Lab Perkin Reaction Organic REActivity PERKIN REACTION (ALDOL CONDENSATION) The Reaction Scheme: Formation of trans-cinnamic acid The following reaction is named the Perkin Reaction. It is a very specific type of Aldol condensation that forms a variety of cinnamic acid derivatives. In this lab, you will perform a Perkin reaction using benzaldehyde and potassium carbonate in acetic anhydride to form trans- cinnamic acid (1). Trans-cinnamic acid is a natural compound found in...
How do I find the theoretical masses of the elimination product and the addition product? The molecular weights are provided in table Aldol Addition and Condensation Alm. You will perform two reactions, one of which is an aldol addition and one provides the aldol condensation product. Both procedures will be performed ALDOL ADDITION conditions ALDOL CONDENSATION MSDS - ME Reactants Table Reactant(s) 2-acetylpyridine 4-nitrobenzaldehyde methanol Sodium carbonate water MW Density BPMP D 11.12 12.04 USD ROISS 0.180 MW BP MP...
Question- The second step is a name reaction. a) What is its name: b) Is it OK that we left the reaction in our drawer over the week? What would have happened if we didn’t have a good seal on the stopper? Draw a possible reaction scheme. Background The field of medicinal chemistry combines the specialties of synthetic organic chemistry and biology, and biochemistry. Compounds are generated and biological activity is screened using target specific assays. . These assays are...
In this Diels-Alder reaction, what is the limiting reagent for this reaction? Please show work In this experiment, a Diels-Alder reaction will be performed to generate 4-cyclohexene- 1,2-dicarboxylic anhydride. The reaction occurs when 1,3-butadiene is combined with maleic anhydride and heated as shown below. Once the product has been isolated, the IR spectrum, melting point, and experimental yield can be determined. 5.- I111NI O Due to the inherent difficulties with the handling of gaseous 1,3-butadiene, it will be generated in...
are there any synthetic transformations produced in this lab Step 1. Preparation and Recrystallization of a Diastereomeric Salt - Synthesis of (R,R)-1,2-Diammoniumcyclohexane mono-(+)-tartrate: In a 150 ml beaker, L-(+)-Tartaric acid (7.5 g, 0.05 mol) is dissolved in 25 mL of distilled water. The solution is stirred as 11.4 g (12.2 mL, 0.10 mol) of 1,2-diaminocyclohexane is added carefully in one portion. (The addition of the diamine is exothermic.) A slurry is formed initially but complete dissolution is observed once addition...
Make a purpose statement synthesis equation table of contents and theoretical yield for the synthesis of veratraldehyde oxime ( example given) NITRILE 1. SYNTHESIS oF VERATRALDEHYDE oxiME Review From previous lab procedures: suction filtration, recrystallization From organic chemistry text: sections 18.15, 18.16 Introduction oximes are usually prepared as derivatives of aldehydes and ketones, and they are used as a means of characterizing them and them. However, be reduced to amines or dehydrated to yield nitriles. Thus, they are also useful...
please write a balanced eqaution for this reaction We were unable to transcribe this imageLab 8: Preparation of an a B-Unsaturated Ketone via Michael and Aldol Condensation Reactions of an a, B-Unsaturated Ketone via Michael and Aldol Condensation Reactions Finally, the aldol intermediate is dehydrated to form the final product, 6-ethoxycarbonyl-3,5-diphenyl-2-cyclohexenone. The a Bunsaturated ketone that is formed is very stable because of the conjugation of the double bond with both the carbonyl group and a phenyl group. CH2Et-O CH...
1.) What side reactions occur during the following steps. 2.) How can the IR spectrum be used to show that there is not starting material left and the products are ketones? 3.) Describe the major differences and similarities between the IR spectra of benzoin and benzil. Compare your IR spectrum with those of benzoin and benzil. Copper-Catalyzed Oxidation of Benzoin 1. Add a stir bar and 1.5 mL of glacial acetic acid, 0.250 g of NH4NO3 and 0.500 g of...
Hi! Can you please answer questions a and b for my organic lab report :) The pictures below the questions is my lab procedure. Thank you 6. Analysis Questions: a) This lab utilized a new technique called reflux, and the use of a condenser tube while heating the reaction. What is the purpose of the condenser? Why not just heat the reaction in a closed vessel instead? b) A student misread the instructions and first refluxed the sodium methoxide in...