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- c) Aldol – from start to finish NaOEt, ETOHDraw the products formed in the crossed aldol reaction of phenylacetaldehyde (C6H5CH2CHO) with each compound: (a) CH2(COOEt)2; (b) CH2(COCH3)2; (c) CH3COCH2CN.Draw all potential aldol renction produets. you exuude stereachmisty and may that no condensaton reuction asSume occur NaocHzcH3 t aldol reaution
- 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. Illustrate detailed mechanisms for below attempted aldol reaction. CH3 CH ? Na OH ČH3Q1: Product of aldol condensation H 0^6= + NaOH Ethanol A) B) C) D) ör ör od or
- O Answer (d) QUESTION 6 Which one of the following compounds does not undergo an aldol reaction with itself when treated with NaOEt in EtOH? H. (a) (b) (c) CH3 (d) (cH); C H. O Answer (a) O Answer (b) O Answer (c) O Answer (d) QUESTION 7 What is the major organic product after the following two reaction steps ?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 :ÓH :OH ö:18) What two organic starting materials are required to produce cinnamaldehyde (PhCH=CHCHO) via a crossed aldol condensation followed by dehydration? A) PhCH3 and CH3CHO B) PhCHO and CH3CHO C) PhCHO and CH3CH2CHO D) PhCHO and CH3CH₂OH b