Chemistry, asked by harsithasrinivasan, 8 months ago

write cross adol condensation products of benzaldehyde and ethanal​

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Answered by anjali962
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The reactivity of benzaldehyde and ethanal towards nucleophilic addition reactions : Bezaldehyde is less reactive than ethanal .Explanation:Nucleophilic addition

The reactivity of benzaldehyde and ethanal towards nucleophilic addition reactions : Bezaldehyde is less reactive than ethanal .Explanation:Nucleophilic additionThe  nucleophilic addition reaction is an addition reaction in which a chemical compound having double or triple bond,  reacts with electron-rich reactant, termed a nucleophile and as a result single bond in place of double is formed .

The reactivity of benzaldehyde and ethanal towards nucleophilic addition reactions : Bezaldehyde is less reactive than ethanal .Explanation:Nucleophilic additionThe  nucleophilic addition reaction is an addition reaction in which a chemical compound having double or triple bond,  reacts with electron-rich reactant, termed a nucleophile and as a result single bond in place of double is formed .Comparison of reactivity of Benzaldehyde and ethanal towards nucleophilic addition reaction .

The reactivity of benzaldehyde and ethanal towards nucleophilic addition reactions : Bezaldehyde is less reactive than ethanal .Explanation:Nucleophilic additionThe  nucleophilic addition reaction is an addition reaction in which a chemical compound having double or triple bond,  reacts with electron-rich reactant, termed a nucleophile and as a result single bond in place of double is formed .Comparison of reactivity of Benzaldehyde and ethanal towards nucleophilic addition reaction .The carbon atom of the carbonyl group of benzaldehyde is less electrophilic than carbon atom of the carbonyl group present in ethanal. The polarity of the carbonyl group is reduced in benzaldehyde due to resonance hence less reactive than ethanal.

The reactivity of benzaldehyde and ethanal towards nucleophilic addition reactions : Bezaldehyde is less reactive than ethanal .Explanation:Nucleophilic additionThe  nucleophilic addition reaction is an addition reaction in which a chemical compound having double or triple bond,  reacts with electron-rich reactant, termed a nucleophile and as a result single bond in place of double is formed .Comparison of reactivity of Benzaldehyde and ethanal towards nucleophilic addition reaction .The carbon atom of the carbonyl group of benzaldehyde is less electrophilic than carbon atom of the carbonyl group present in ethanal. The polarity of the carbonyl group is reduced in benzaldehyde due to resonance hence less reactive than ethanal.Cross aldol condensation

The reactivity of benzaldehyde and ethanal towards nucleophilic addition reactions : Bezaldehyde is less reactive than ethanal .Explanation:Nucleophilic additionThe  nucleophilic addition reaction is an addition reaction in which a chemical compound having double or triple bond,  reacts with electron-rich reactant, termed a nucleophile and as a result single bond in place of double is formed .Comparison of reactivity of Benzaldehyde and ethanal towards nucleophilic addition reaction .The carbon atom of the carbonyl group of benzaldehyde is less electrophilic than carbon atom of the carbonyl group present in ethanal. The polarity of the carbonyl group is reduced in benzaldehyde due to resonance hence less reactive than ethanal.Cross aldol condensationIt is a reaction in which two different molecules are condensed together .

The reactivity of benzaldehyde and ethanal towards nucleophilic addition reactions : Bezaldehyde is less reactive than ethanal .Explanation:Nucleophilic additionThe  nucleophilic addition reaction is an addition reaction in which a chemical compound having double or triple bond,  reacts with electron-rich reactant, termed a nucleophile and as a result single bond in place of double is formed .Comparison of reactivity of Benzaldehyde and ethanal towards nucleophilic addition reaction .The carbon atom of the carbonyl group of benzaldehyde is less electrophilic than carbon atom of the carbonyl group present in ethanal. The polarity of the carbonyl group is reduced in benzaldehyde due to resonance hence less reactive than ethanal.Cross aldol condensationIt is a reaction in which two different molecules are condensed together .Ethanal and Benzaldehyde  react in presence of concentrated KOH to form Para alkokxy benzyl alcohol .

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