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3-Pentanone does not give a positive iodoform test because it lacks the necessary structure. The iodoform test specifically requires the presence of a methyl ketone (a ketone with a methyl group adjacent to the carbonyl), which 3-pentanone does not have; its structure is CH3(CH2)3COCH3. Instead, it features a propyl group adjacent to the carbonyl, preventing the formation of iodoform (CHI3) upon reaction with iodine and a base.
The molecular mass of 2-pentanone (C5H10O) is 86.13 g/mol.
1-Propanol and 3-pentanone can be distinguished using the oxidation test with potassium dichromate (K2Cr2O7). 1-Propanol, a primary alcohol, will oxidize to form propanoic acid, resulting in a color change from orange to green. In contrast, 3-pentanone, a ketone, is resistant to oxidation under these conditions and will not produce a color change. This difference in reactivity allows for the identification of the two compounds.
2-pentanone is a ketone with a carbonyl group attached to a five-carbon chain, while 2-pentanol is an alcohol with the -OH group attached to the same five-carbon chain. 2-pentanone has a carbonyl group, giving it a characteristic ketone odor. 2-pentanol is an alcohol, making it more polar and having different physical properties compared to 2-pentanone.
The formula is C5H9BrO.
3-Pentanone does not give a positive iodoform test because it lacks the necessary structure. The iodoform test specifically requires the presence of a methyl ketone (a ketone with a methyl group adjacent to the carbonyl), which 3-pentanone does not have; its structure is CH3(CH2)3COCH3. Instead, it features a propyl group adjacent to the carbonyl, preventing the formation of iodoform (CHI3) upon reaction with iodine and a base.
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Ch3ch2coch2ch3
They are metamers but not position isomers
CH3-CH(=O)-CH(CH3)-CH2-CH3
No, 2-pentanone would not give a positive reaction to the Iodoform test. The Iodoform test is specific for methyl ketones (ketones with a methyl group adjacent to the carbonyl), and 2-pentanone does not have this structure. Instead, it has a butyl group adjacent to the carbonyl, which does not lead to the formation of iodoform.
mthyl propyl keton
Do an iodoform test. Use an aqueous solution of iodine and potassium iodide added to basic solutions of 2-pentanone and 3-pentanone.The iodoform reaction is a classical test for methyl ketones. A light-yellow precipitate of iodoform forms immediately with the methyl ketone of 2-pentanone.To confirm:1H NMR3-pentanone will show only 2 signals: a triplet at ~1.33 and a quartet at ~2.352-pentanone will show 4 signals: a triplet at ~0.90, a sextet at ~1.55, a singlet at ~2.05 and a triplet at ~2.40
2-pentanone IS a chemical. One place it's found is in tobacco.
The molecular mass of 2-pentanone (C5H10O) is 86.13 g/mol.
1-Propanol and 3-pentanone can be distinguished using the oxidation test with potassium dichromate (K2Cr2O7). 1-Propanol, a primary alcohol, will oxidize to form propanoic acid, resulting in a color change from orange to green. In contrast, 3-pentanone, a ketone, is resistant to oxidation under these conditions and will not produce a color change. This difference in reactivity allows for the identification of the two compounds.
2-pentanone is a ketone with a carbonyl group attached to a five-carbon chain, while 2-pentanol is an alcohol with the -OH group attached to the same five-carbon chain. 2-pentanone has a carbonyl group, giving it a characteristic ketone odor. 2-pentanol is an alcohol, making it more polar and having different physical properties compared to 2-pentanone.