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.

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3 years ago

Complete the table below by deciding whether a precipitate forms when aqueous solutions A and B are mixed. If a precipitate will

stiks02 [169]

The reaction between copper II chloride and sodium sulfide as well as lead II nitrate and potassium sulfate both produce precipitates.

The solubility of a substance in water is in accordance with the solubility rules. It is possible that a solid product may be formed when two aqueous solutions are mixed together. That solid product is referred to as a precipitate.

Now, we will consider each reaction individually to decode whether or not a precipitate is possible.

In the first reaction, we have; CuCl2(aq) + Na2S(aq) ---->CuS(s) + 2NaCl(aq). A precipitate (CuS) is formed.
In the second reaction, Pb(NO3)2(aq) + 2KNO3(aq) ----> PbSO4(s) + KNO3(aq), a precipitate PbSO4 is formed
In the third reaction, NH4Br(aq) + NaOH(aq) ----->NH3(g) + NaBr(aq) + H2O(l), a precipitate is not formed here.

Learn more: brainly.com/question/11969651

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