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Skeletal formula:
HO-C(=O)-CH2CH(-OH)-C(=O)-OH
Molecular formula:
C4H6O5
Wiki User
∙ 13y ago
Wiki User
∙ 13y agoMalic acid melts at 130 degrees C.
It doesn't really boil, but it will decompose instead at 140 degrees C to produce carbon monoxide, carbon dioxide, maleic acid and maleic anhydride.
Wiki User
∙ 11y agothe ph is ph 6
Wiki User
∙ 13y agoManganic acid would be H2MnO4
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∙ 13y agoHOOC-CH2-COOH
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∙ 12y agoFormula: H2MnO4
Wiki User
∙ 11y agoThis formula is CH2(COOH)2.
Wiki User
∙ 13y agoC4H6O5
Wiki User
∙ 11y agoC3h4o4
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Why Oxalic acid is stonger than malonic acid?
A strong acid has a stabilized conjugate base. Oxalic acid is stronger than malonic acid because its conjugate base has much more resonance structures than malonic acid's conjugate base.
What carboxylic acid would decarboxylate by heating?
A classic example of a carboxylic acid decarboxylation occurs in the malonic ester synthesis. The malonic ester synthesis is a chemical reaction where diethyl malonate or another ester of malonic acid is alkylated at the carbon alpha (directly adjacent) to both carbonyl groups, and then converted to a substituted acetic acid. Malonic acid is another example of an acid that will decarboxylate when heated (not sure at what temperature this happens, though)The structure of malonic acid is HOOC-CH2-COOH.
How many protons can be lost by acetic acid HC2H3O2?
Malonic acid has pKa values of 2.83 (pK1) and 5.69 (pK2). If malonic esters are used then on treatment with a strong base like sodium ethoxide, the methylene (-CH2-) hydrogen can be deprotonated, but I am not sure if that is possible for malonic acid as that will lead to a tri-anion.
Is malonic acid a diprotic acid?
Yes, it is diprotic, HOOC-CH2-COOH
When malonic acid is heated with P2O5 what is formed?
Carbon Suboxide
Why Oxalic acid is stonger than malonic acid?
A strong acid has a stabilized conjugate base. Oxalic acid is stronger than malonic acid because its conjugate base has much more resonance structures than malonic acid's conjugate base.
How do you find the emperical value?
emperical formula- CH2
What carboxylic acid would decarboxylate by heating?
A classic example of a carboxylic acid decarboxylation occurs in the malonic ester synthesis. The malonic ester synthesis is a chemical reaction where diethyl malonate or another ester of malonic acid is alkylated at the carbon alpha (directly adjacent) to both carbonyl groups, and then converted to a substituted acetic acid. Malonic acid is another example of an acid that will decarboxylate when heated (not sure at what temperature this happens, though)The structure of malonic acid is HOOC-CH2-COOH.
What is Malonic acids role with respect to succinate dehydrogenase?
Malonic acid is a competitive inhibitor of succinate dehydrogenase.
How many protons can be lost by acetic acid HC2H3O2?
Malonic acid has pKa values of 2.83 (pK1) and 5.69 (pK2). If malonic esters are used then on treatment with a strong base like sodium ethoxide, the methylene (-CH2-) hydrogen can be deprotonated, but I am not sure if that is possible for malonic acid as that will lead to a tri-anion.
Is malonic acid a diprotic acid?
Yes, it is diprotic, HOOC-CH2-COOH
When malonic acid is heated with P2O5 what is formed?
Carbon Suboxide
What is the purpose of using malonic acid in this experiment?
it is a competitive inhibitor
What is the empirical formula for the compound x3y12?
The emperical formula is XY4
What is the emperical formula of water?
The empirical formula of water is H2O.
What is the emperical formula for Sr and F?
SrF2
A solution of malonic acid h2c3h2o4 was standardized by titration with 0.1000 M Naoh solution if 20.76 ml of the naoh solution were required to neutralize completely 13.15 ml of malonic acid solution?
.0899M
