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The structure of 3-oxopentanoic acid consists of a pentanoic acid molecule with a ketone group (3-oxo group) attached to the third carbon atom of the carbon chain. It is also known as 3-oxovaleric acid.
The salt produced from the reaction between KOH (potassium hydroxide) and pentanoic acid is potassium pentanoate. This salt is formed by the neutralization reaction between the potassium ion from KOH and the pentanoate ion from pentanoic acid.
The molar mass of 1-pentanoic acid (C5H10O2) is approximately 102.13 g/mol.
You can oxidize 1-pentanol using an oxidizing agent such as chromic acid or potassium permanganate to form pentanoic acid. This reaction typically requires heat and can be catalyzed by sulfuric acid. Purification techniques like distillation can help isolate the pentanoic acid product.
The product of the reaction of pentanoic acid with ethanol in the presence of a strong acid is ethyl pentanoate, also known as pentanoic acid ethyl ester. The reaction is an esterification process, where the carboxylic acid (pentanoic acid) reacts with the alcohol (ethanol) to form the ester, releasing water as a byproduct.
The structure of 3-oxopentanoic acid consists of a pentanoic acid molecule with a ketone group (3-oxo group) attached to the third carbon atom of the carbon chain. It is also known as 3-oxovaleric acid.
Pentanoic acid.
The salt produced from the reaction between KOH (potassium hydroxide) and pentanoic acid is potassium pentanoate. This salt is formed by the neutralization reaction between the potassium ion from KOH and the pentanoate ion from pentanoic acid.
The molar mass of 1-pentanoic acid (C5H10O2) is approximately 102.13 g/mol.
1-pentanol
It is lactic acid... I am 100% sure that it is wrong
You can oxidize 1-pentanol using an oxidizing agent such as chromic acid or potassium permanganate to form pentanoic acid. This reaction typically requires heat and can be catalyzed by sulfuric acid. Purification techniques like distillation can help isolate the pentanoic acid product.
The product of the reaction of pentanoic acid with ethanol in the presence of a strong acid is ethyl pentanoate, also known as pentanoic acid ethyl ester. The reaction is an esterification process, where the carboxylic acid (pentanoic acid) reacts with the alcohol (ethanol) to form the ester, releasing water as a byproduct.
When methanol is heated with pentanoic acid, an esterification reaction occurs, forming methyl pentanoate (a type of ester) and water as byproduct. This reaction is catalyzed by an acid suchanni acid.
There are 4 isomers of carboxylic acids for this formula CH3-CH2-CH2-CH2-COOH pentanoic acid, CH3-CH(CH3)-CH2-COOH 3-methyl butanoic acid, CH3-CH2-CH(CH3)-COOH 2-methyl butanoic acid and CH3-C(CH3)2-COOH dimethyl propanoic acid.
Butanoic acid is more water soluble than butane. This is because butanoic acid can form hydrogen bonds with water molecules due to its polar functional group (carboxyl group), whereas butane is a nonpolar molecule and cannot easily interact with water molecules.
Yes, sulfuric acid is a molecule with the formula H2SO4