give the reaction to convert malic acid to maleic acid
Answers
Introduction:
Malic acid is an alpha hydroxy acid that may be found in a variety of fruits and wines. It's found in foods, cosmetics, and even medication. Malic acid is a sour and acidic substance.
Maleic acid is an organic white crystalline solid chemical with two carboxyl functional groups (-COOH) molecules.
Explanation:
Maleic acid, also known as cis-butenedioic acid, is a dicarboxylic acid, or molecule containing two carboxyl groups. It has the chemical formula HO2CCH=CHCO2H. Butenedioic acid has two isomers: cis-isomer maleic acid and trans-isomer fumaric acid. Maleic acid has limited uses in comparison to its parent, maleic anhydride, and is mostly employed as a precursor to fumaric acid.
C4H4O is the chemical formula.
Fumaric acid, succinic acid, and crotonic acid are related carboxylic acids.
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Answer:
Concept:
Malic acid is an alpha hydroxy acid found in certain fruits and wines. It's used in foods and cosmetics, and sometimes as medicine.
Maleic acid is an organic compound and the cis-isomer form of the butenedioic acid.
Find:
give the reaction to convert malic acid to maleic acid
Given:
give the reaction to convert malic acid to maleic acid
Explanation:
Malic acid is an alpha hydroxy acid found in certain fruits and wines. It's used in foods and cosmetics, and sometimes as medicine.
Malic acid is sour and acidic. This helps to clear away dead skin cells when applied to the skin. Its sourness also helps to make more saliva in people with dry mouth. Malic acid is also involved in the Krebs cycle. This is a process the body uses to make energy. People commonly use malic acid for dry mouth. It is also used for acne, fibromyalgia, fatigue, wrinkled skin, and many other conditions, but there is no good scientific evidence to support these uses.
Malic acid is an alpha hydroxy acid. Don't confuse it with other alpha hydroxy acids (AHAS).
Maleic acid is an organic compound and the cis-isomer form of the butenedioic acid. Hence, maleic acid is a dicarboxylic acid which means that the maleic acid structure consists of two carboxyl groups. The maleic acid molecular formula is HOOCCH=CHCOOH, which clearly shows the presence of the double bond of carbon as depicted by the name butenedioic acid. This can also be seen in maleic acid IUPAC name or nomenclature which identifies maleic acid as (2Z) But-2-enedioic acid. The heat of combustion of maleic acid is -1335 kJ/mol and is higher than the fumaric acid.
Also, maleic acid and fumaric acid have different solubility properties as well. Maleic acid is more soluble in water than the trans counterpart fumaric acid.
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