b) Ethylgrignard o get butan-3-ol and then treat it with chlorine in the presence of light to give 1 chloro compound and then aquous KOH to give the product reqd
Acetaldehyde can be converted to butane-1,3-diol in a two-step process. First, acetaldehyde is reduced to 1,3-propanediol using a reducing agent like sodium borohydride. Then, 1,3-propanediol can be dehydrated to form butane-1,3-diol using an acid catalyst, such as sulfuric acid.
Acetaldehyde can be obtained by reduction of acetic acid CH3COOH+2[H]--------------CH3CHO+H2O
A larger percentage of persons of Asian decent, have a dominant gene mutation which interferes with the role of an enzyme called acetaldehyde dehydrogenase. The role of this enzyme is to convert acetaldehyde, a metabolite of ethanol (alcohol), into acetic acid. Persons with this mutation therefore experience higher levels of acetaldehyde in their systems when they consume alcohol.
The cyclic polymerization of acetaldehyde results in several products. These include paraldehyde, metaldehyde, and polyacetaldehyde which are all polymers of acetaldehyde.
What is the best route for synthesis of pyridine-4-acetaldehyde?
Acetaldehyde
Yes.
No...
Vinyl chloride is CH2=CHCl, and acetaldehyde is CH3CHO and both are not tautomers. The isomer of acetaldehyde is CH2=CHOH, but is generally unstable and converts back to acetaldehyde.
Are you sure it is acetatdehyde not acetaldehyde.
Acetaldehyde was discovered in 1774. It was a Swedish chemist and pharmacist named Carl Wilhelm Scheele who first discovered the chemical compound.
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When alcohol is oxidized it becomes acetaldehyde, which is toxic. The acetaldehyde quickly become acetate, and then finally carbon dioxide and water.