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:
1) 40
2) 2.25 moles
3) 17
4) 120
5) Fe₂O₃
Explanation:
Please see attached picture for full solution.
Answer:
The specific heat of water is 4.18 J/g C.
Explanation:
q
=
m
C
s
Δ
T
Never forget that!
2200
=
m
⋅
4.18
J
g
⋅
°
C
⋅
66
°
C
∴
m
≈
8.0
g
The answer is A. As the first statement is a true statement. Hope this help you
