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- What is the reactant that would give the following Aldol Condensation product? 01 0 | 0 ||| O IV OV H H تبار نہید لبد بد مبد IV :O: ة :0: :0: :O:18en the folbwng sequence of reac ond what wo structure of compound AT D (CH,,CULI 2) H,0 HN-CH, H,0 Select one 2.Wnchufthfollewine.comectly represert eet the stepm the rechnsnetamad altalcardensation reactDraw the mechanism of the following alkylation reaction that occurs via an enolate intermediate. о сн, о сн, (1) LDA Ph-C-CH-CH, Ph-C-C-CH, (2) Ph — CH, — Вr ČH,-Ph
- ArSO,H Draw curved arrows to show the movement of electrons in the following step of an acid-catalyzed aldol condensation reaction. Arrow-pushing Instructions Hjö: H-Ö- -Ar H. Ar O=h=02 CH3COOCH,CH3 C2H5O'K*/C2H5OH ---> CH3COCH,COOCH,CH3 [+] Hofmann elimination Clemmensen reduction Claisen condensation O Cannizzaro reaction O Aldol condensationArSO;H Draw curved arrows to show the movement of electrons in the following step of an acid-catalyzed aldol condensation reaction. Arrow-pushing Instructions :ÓH :OH ö:
- What are the products of an aldol cyclization for the following compound?The given reaction scheme is an example of which type of reaction? O || R₁-C-OH + R₂-OH Oxidation Fischer esterification Nucleophilic substitution Reduction Rearrangement reaction Acid O || R₁-C-O-R₂ Meeting in "General"Complete the following reaction of hydrolysis using arrows and drawing the intermediate products Catión estabilizado por resonancia Catión oxonio MeO OMe - MeOH R R Acetal Catión oxonio Catión oxonio Meo OH R- R Hemiacetal MeOH Catión estabilizado por resonancia -H® R R Compuesto carbonilico
- Draw the mechanism for the following reaction H2O + он онIdentify a type of reaction that can be used to prepare the compound below without the need for any further reactions. MeO O Conjugate addition O enolate alkylation O Claisen condensation O aldol reaction Submit AnswThe following isomerization reaction, drawn using D-glucose as starting material, occurs with all aldohexoses in the presence of base. Draw a stepwise mechanism that illustrates how each compound is formed. сно сно сно CH2OH C=0 H- OH H- -OH но- H- но H- "OH но H- Но H- но H- H- -H- H20 H- HO- O- H- -O- H- -OH -O- OH ČHOH CH,OH ČH2OH ČH2OH (recovered starting material) D-glucose