2-Methyl-4-oxo-pentanoic acid is unlikely to produce 2-Methyl-3-butanone upon strong heating.
Upon heating, the β ketoacid becomes unstable and decarboxylates, leading to the formation of the methyl ketone.
A carboxylic acid is an organic acid that contains a carboxyl group (C(=O)OH) attached to an R-group. The general formula of a carboxylic acid is R−COOH or R−CO2H, with R referring to the alkyl, alkenyl, aryl, or other group.
Carboxylic acids occur widely. Important examples include the amino acids and fatty acids. Deprotonation of a carboxylic acid gives a carboxylate anion.
Full question :
Q. Which reactant is unlikely to produce the indicated product upon strong heating?
- A) 2,2-Dimethylpropanedioic acid 2-methylpropanoic acid
- B) 2-Ethylpropanedioic acid Butanoic acid
- C) 2-Methyl-3-oxo-pentanoic acid 3-Pentanone
- D) 2-Methyl-4-oxo-pentanoic acid 2-Methyl-3-butanone
- E) 4-Methyl-3-oxo-heptanoic acid 3-Methyl-2-hexanone
Hence, option (D) is correct.
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In ionic bonding, an arrow is often drawn on the diagram to show the direction the electrons move to form the ions.
Just find Ag and F on periodic table, find g/mol for each one and add them together
The word elliptical refers to an Oval.
Answer: B
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