1. Predict the organic product(s) from the following reactions. Draw the curved arrows for the carbon-carbon bond-forming step (enolate attacking carbonyl) in the box under the starting materials. 1. LDA (1 equiv), -78 °C 2. Ph 3. H3O+ workup curved arrows for enolate attacking carbonyl KOEt (cat) EtOH (solvent) heat H₂N major product(s) (including stereoisomers if relevant) curved arrows for enolate attacking carbonyl major product(s) (including stereoisomers if relevant) + H2O

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1. Predict the organic product(s) from the following reactions. Draw the curved arrows for the carbon-carbon
bond-forming step (enolate attacking carbonyl) in the box under the starting materials.
1. LDA (1 equiv), -78 °C
2.
Ph
3. H3O+ workup
curved arrows for enolate attacking carbonyl
KOEt (cat)
EtOH (solvent)
heat
H₂N
major product(s) (including stereoisomers if relevant)
curved arrows for enolate attacking carbonyl
major product(s) (including stereoisomers if relevant) + H2O
Transcribed Image Text:1. Predict the organic product(s) from the following reactions. Draw the curved arrows for the carbon-carbon bond-forming step (enolate attacking carbonyl) in the box under the starting materials. 1. LDA (1 equiv), -78 °C 2. Ph 3. H3O+ workup curved arrows for enolate attacking carbonyl KOEt (cat) EtOH (solvent) heat H₂N major product(s) (including stereoisomers if relevant) curved arrows for enolate attacking carbonyl major product(s) (including stereoisomers if relevant) + H2O
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