Indicate if the aldehyde shown reacts with the provided nucleophiles in acid or base conditions. a NaBH4 be Li eli -NH2 P(Ph3) f KCN g OH excess h CH3OH i NaCHCCH3
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
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- Which of the following is the most reactive to a nucleophile? ethyl ethanoate O ethanoyl chloride ethnic anhydride acetophenone O chlorobenzeneRank the following nucleophiles in order from slowest SN2 reaction rate to fastest if DMSO is the solvent. ОН PH SH A B D EWhich of the following could act as a nucleophile? O CH3NH₂ O HCI O BF3 O CH₂Br 4 Previous
- Which of the following compound is least likely to undergo a nucleophilic substitution reaction?what is the mechanism for this reaction and would be the structure of the product?Which of the following nucleophiles would add to an alpha,beta-unsaturated ketone via direct addition? KCN LICH3 KOH NH,CH,CH,CH3 O HOCH₂CH₂CH3
- Can you explain the mechanism for this question HO OH H2SO4 cat. H₂OWhich of the following is not the result of a nucleophilic addition to a ketone or aldehyde?Rank the following carbonyl-containing compounds in order of reactivity towards nucleophilic acyl substitution. Most reactive Least reactive Answer Bank N,N-diphenylethanamide acetyl chloride butyl acetate acetic anhydride
- The following reaction involves two sequential Heck reactions. Draw structural formu- las for each organopalladium intermediate formed in the sequence and show how the final product is formed. Note from the molecular formula given under each structural formula that this conversion corresponds to a loss of H and I from the starting material. Acetonitrile, CH,CN, is the solvent. 1% mol Pd(OAc), 4% mol Ph,P CH,CN C4H171 C4H16Please complete the mechanism of the following reaction.Which statement(s) is(are) true concerning the rate-limiting step involving the benzene ring? CI AICI3 O aromaticity is restored aromaticity is disrupted proton transfer occurs carbocation intermediate forms O the benzene ring functions as the nucleophile the benzene ring functions as the electrophile
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