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Look at each of the given compounds and determine if they would be a nucleophile only, an electrophile only, both, or neither for an aldol condensation. Compound A: electrophile only Compound B: nucleophile only Compound C: both an electrophile and a nucleophile Compound D: neither Compound E: both an electrophile and a nucleophile Compound F: nucleophile only

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Understanding aldol condensation helps determine whether a compound acts as an electrophile, a nucleophile, both, or neither.
Key ideas:
- The electrophile in an aldol reaction is typically a carbonyl compound (aldehyde or ketone) whose carbonyl carbon can be attacked by a nucleophile.
- The nucleophile in an aldol reaction is usually an enolate or an enolizable species that can form a negatively charged carbon (or a highly nucleophilic center) to attack the electrophile.
- A molecule can act as an electrophile, a nucleophile, both, or neither depending on its structural features (presence of a carbonyl group for electrophilicity and presence of ......Login to view full explanationLog in for full answers
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Similar Questions
Look at each of the given compounds and determine if they would be a nucleophile only, an electrophile only, both, or neither for an aldol condensation. Compound A: electrophile only Compound B: nucleophile only Compound C: both an electrophile and a nucleophile Compound D: neither Compound E: both an electrophile and a nucleophile Compound F: nucleophile only
Put the mechanism steps in order for an aldol condensation. (Not all steps may be used) 1: First Mechanism Process 2: Second Mechanism Process 3: Third Mechanism Process
Which of these is the final product for an aldol condensation if heated?
Which of these is an intermediate structure for an aldol condensation? (select all that apply)
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