Answer:
Extreme heat will cause the substance molecules to move faster and cause a phase change this phase change would occur if left in an extremely hot area causing the molecules to spread apart.
Explanation:
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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Answer: 
Explanation:
According to the law of conservation of mass, mass can neither be created nor be destroyed. Thus the mass of products has to be equal to the mass of reactants. The number of atoms of each element has to be same on reactant and product side. Thus chemical equations are balanced.
The balanced equation will be:
the answer is Te because O is oxygen.
