If a student is starting with diethylmalonate then the base they would use to generate the enolate would beNaOMeNaOEtNaOHNone of the above.The synthesis of dibenzalacetone is an example ofDieckmann condensationAldol condensationMichael reactionNone of the above.Starting with a 1,6 - diester and treating it with NaOEt would be an example of Aldol CondensationClaisen CondensationDieckmann CondensationNone of the above. A nucleophile that adds to the beta carbon of an alpha, beta unsaturated aldehyde or ketone would be considered HardSoftAcidicNone of the above.

These are example of nucleophilic addition reaction

Answered: If a student is starting with…

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter14: Elimination

Section: Chapter Questions

Problem 35CTQ

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If a student is starting with diethylmalonate then the base they would use to generate the enolate would be

NaOMe

NaOEt

NaOH

None of the above.

The synthesis of dibenzalacetone is an example of

Dieckmann condensation

Aldol condensation

Michael reaction

None of the above.

Starting with a 1,6 - diester and treating it with NaOEt would be an example of

Aldol Condensation

Claisen Condensation

Dieckmann Condensation

None of the above.

A nucleophile that adds to the beta carbon of an alpha, beta unsaturated aldehyde or ketone would be considered

Hard

Soft

Acidic

None of the above.

Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.

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