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- Give the IUPAC name of the two carbonyl compounds reacted together to synthesize compound A, given below, by a crossed aldol condensation followed by dehydration. || CH3CCH=CH₂2 A18en 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 reactWhat products are formed when the following molecule reacts with catalytic H2SO4, H2O, and heat? Please show the mechanism for the reaction.
- What are the expected major products for the following reaction sequence?Which of the following can undergo an aldol self-condensation and yield multiple (different) self-condensation products? A H₂ H3C g CH3 H B D H₂ se H₂ H3C H3C CH3 HQ1/A) Arrange the following sets of compounds in order of: 1) Increasing acidity H₂C CH₂ H₂C OCH₂CH₂ OCH₂CH3 Ph, изза паззакон показзаки здають 2) Increasing yield in cross Aldol condensation p-methyl benzaldehyde, p-methoxy benzaldehyde, benzaldehyde, p-nitro benzaldehyde 3) Stability of carbanion ion O 11 유 CH3-CN, CH3-C-OCH3. CH3-C-CH3, CH3NOz
- What is the synthesis and mechanism for the following?Which of A to E shows the product that will be obtained from the reaction of (Z)-hex-2-ene with MeCO3H?The first step in the mechanism of reduction of an aldehyde or ketone with either LiAlH4 or NaBH4 is nucleophilic attack. Which of the following is the electrophilic site in this first step?
- The intramolecular Aldol condensation of 2,6-heptancdione with base may produces two possible Bhydroxyl ketones as shown in the following reaction pathway. CH, (1) OH CH, (A) 3-Methyl-2-cyclohexenone .CH, CH, (2) OH - CH3 2,6-Heptanedione (B) Methyl(2-methyl-1-cyclobutenyl)ketone Write detailed mechanisms for both the reactions (1) and (2).Provide the product of the following cross aldol condensation: s H HBr O CF3 H CH₂Cl2Provide the major product of the following crossed aldol condensation reactions. Assume dehydration occurs in each case. H₂C HO =O + H3C H3C CH3 CH3 CH3 NaOH, EtOH heat KOH, EtOH heat NaOH, EtOH heat