Tabulations of chemical elements differing in their organization from the traditional seen periodic system
Benzaldehyde or C6H5CHO would not undergo the aldol condensation because it does not contain an alpha-hydrogen in its structure. Aldol condensation is a type of reaction that happens between an enolate and an aldehyde or ketone leading to a alkene that has a planar structure. The lack of an alpha-hydrogen would not allow for it to undergo such process since it cannot enolize. Benzaldehyde undergoes a nucleophilic reaction known as Claisen-Schmidt condensation. It has somehow same mechanism of the aldol reaction however, the nucleophilic attack on the carbonyl happens even without the alpha-hydrogen but with an enolate that is from a ketone.
Answer:
The stronger conjugate base will be the weaker acid; i.e., the acid with the smaller Ka-value.
Explanation:
Given conjugate base CN⁻ => weak acid => HCN => Ka =4.9 x 10⁻¹⁰
Given conjugate base OCN⁻ => weak acid=> HOCN => Ka = 3.5 x 10⁻⁴
Ka(HCN) << Ka(HOCN) => CN⁻ is a much stronger conjugate base than OCN⁻
Answer:
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Explanation:
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