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Do carboxylic acids get oxisidized

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Anonymous

15y ago
Updated: 8/18/2019

Yes, to peroxy carboxylic acids.

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Wiki User

15y ago

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Is Carboxylic acid does this contain fat?

No, carboxylic acids are simply a class of organic acids. Some carboxylic acids are fatty acids but are not fats nor do they contain them. Amino acids, the building blocks of protein are also carboxylic acids. One of the most common carboxylic acids is acetic acid, commonly sold as vinegar.


Can LiAlH4 reduce carboxylic acids?

Yes, LiAlH4 can reduce carboxylic acids to alcohols.


Does sodium borohydride reduce carboxylic acids?

No, sodium borohydride does not reduce carboxylic acids.


When compared to sulfric acid how strong are carboxylic acids?

Carboxylic acids are weaker acids than sulfuric acid. This is because carboxylic acids have two weak acidic hydrogen atoms compared to sulfuric acid's strong acidic hydrogen atoms. This makes sulfuric acid a stronger acid than carboxylic acids.


Can sodium borohydride reduce carboxylic acids?

No, sodium borohydride cannot reduce carboxylic acids.


Are glycine and carboxylic acid th same?

No, glycine is one of many different carboxylic acids. Carboxylic acids come in a wide variety ranging from formic acid to amino acids (which include glycine) and fatty acids.


What is the difference between acids and carboxylic acids?

Carboxylic acids are a subtype of acids that contain a carboxyl group (–COOH). Acids, on the other hand, are substances that can release hydrogen ions (H+) in a solution. Carboxylic acids typically have a carboxyl group attached to a carbon atom, giving them distinct chemical and physical properties compared to other types of acids.


Is carboxylic acids inorganic?

No, all the carboxylic acids are organic because they contain carbon and hydrogen and have the living origin.


Are carboxylic acids truly acids?

Yes, they are also organic acids.


Can sodium borohydride effectively reduce carboxylic acids?

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Does the Wolff-Kishner reduction method reduce carboxylic acids?

No, the Wolff-Kishner reduction method does not reduce carboxylic acids.


What is the mechanism of the BH3-THF reaction with carboxylic acids?

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