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- N 3 5 Predicate the products of each reaction: Aldehydes + Ketones CH₂-C-OCH, CH;CH + HC=N =O + H₂NCH₂ OH O + H₂O H H₂SO4 HgSO4 2 H₂ Ni NaCN + NaBH₂ H+ Zn (Hg), HCIWhich of the following is a weak nucleophile? OH- H2O CH3O-Q5. What product is formed when cyclohexanone is reacted with each of the following reagents? MgBr KCN H30 H30 NABH, H30*
- Rank the reactivity of the compounds below toward nucleophilic acyl substitution by writing the compounds' letters in the proper blanks in the box below. `NH CI Br CH3 CH3 A В C E rank compounds for acyl substitution reactivity most least reactive reactive2) When conjugated aldehydes or ketones are attacked by a nucleophile, often more than one product forms. Please show resonance structures to explain which positions in the following conjugated ketone can react with NaBH4. Which product(s) can form? + H н-вн Na H CH3OHQ5. What product is formed when cyclohexanone is reacted with each of the following reagents? MgBr KCN H30* H30 NABH4 H;O*
- Which of the following is the most stable carbanion? Select one: H NH₂ H O H H :Z:I NH₂ NH₂ NH₂O In this step alkyne anion is alting and it is attacking cecting acting as 4 electrophile a Pla وعك Ho as a nucleophile on the genen molecule, which is Br pom 산 2-Bromo propane (26105 576 honros он 2ive the major product(s) of the following reaction. CH,OH, H* NH,
- Among the choices shown, which reagents would lead to 3-pentanone from bromoethane? Al 1 Li Cul 2) C13CH2OTS | BI1 NECNn DMSO 2) CH3CH2M;Br 3)H2O C)CH13CH2-CO CI D CH3CH2-CO OCH2CI13Which of the following reactions could you use to synthesize ethyl acetate: All of these NaO Oi Oi HO CH₂Cl₂ OH Et₂N CH₂Cl₂ Oli HCI EIOH OH EN CH₂Cl₂1. Draw the products for the following substitution reactions: benzylbromide LDA, THE benzylbromide NaOCH3 MEOH benzylbromide LDA, THE benzylbromide NaOCH3 MEOH