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Aldol can react with many substances. Grignard reagents could react with the addition of an alcohol, and this type of reaction was called the Grignard reaction. An addition reaction can occur between the alkyls. Under the effect of diluted base or acid, two molecules of alkyls can interact with each other. The alpha hydrogen in one of the alkyls is added to the oxygen atom of the other alkyls, and the rest is added to the carbon atom of the alkyls to form a beta-hydryl. This reaction is called the aldol condensation reaction. Aldes without alpha hydrogen can undergo an auto-reduction reaction (Conizaro reaction) under basic conditions. In addition, the carbonyls of alkyls and ketones can undergo an addition reaction with H <2>, and the Grignard reagent and the carbonyls in N, N-disubstituted formamides undergo a nuclophile addition to form an intermediate, which is then decomposed to form an alkyls. Fantasy Realm is equally exciting. Everyone is welcome to click and read it!

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The reaction between Fehling's reagent and an aldo will produce a brick-red copper dioxide (Cu2 O). During the reaction, the color of the solution may gradually change from blue to green to yellow to red. If the reaction is fast, the red deposit can be directly observed. <a href="/?from=ask_words" style="color:red" target="_blank">Read more exciting novels for free</a>

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The electropathic reaction was a type of chemical reaction. In the electropathic reaction of an aldo, an electropathic reagent (an electron deficient reagent) attacked the electron rich part of the aldo. Take the electropathic addition reaction between an aldo and an alkene as an example (according to the carbonium intermediate mechanism): the electron cloud density of the pion in the alkene was higher, and it was the part rich in electrons. Due to the strong electron attraction effect of oxygen, the carbonyl-carbon of the carbolic acid had a certain positive electricity and could be used as an electrophile reagent. During the reaction, the carbonyl-carbon of the carbolic acid first approached the electron cloud of the alkene, attracting a pair of electrons to form a carbonium intermediate. During this process, the alkyls acted as electrophiles and attacked the electron rich pi bond of the alkene. After that, other groups (such as the nuclophile) would combine with the carbonium intermediate to complete the reaction. In the nuclophilic addition reaction of an aldo (an aldo can also participate in a nuclophilic reaction, which is opposite to an electrophilic reaction), the carbo carbon of the aldo has a relatively high nuclophilicity. Because of the addition of an electron donating alkyls, the electron density of the carbo carbon is higher than that of the carbo carbon of the aldo. Moreover, the steric hindrance of the ketones is higher than that of the aldo, so the carbo carbon is more likely to undergo a nuclophilic addition reaction than the ketones. This indirectly reflected the characteristics of the carbolic carbon in the reaction and helped to understand the role of the carbolic carbon in the electropathic reaction, because the electronic environment of the carbolic carbon determined its participation in the electropathic reaction and activity. Some organic reactions also involved the electrophilic reaction mechanism of the alkyls. For example, in the Baylis-Hillman reaction, the alkyls were used as electrophiles (the electrophiles in the matrix could be alkyls) to react with the alpha, beta-saturated compounds under the action of a suitable catalyst. This involved the reaction activity of the alkyls as electrophiles and the electron transfer during the reaction. <a href="/?from=ask_words" style="color:red" target="_blank">Read more exciting novels for free</a>