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The most acidic compound is methyl alcohol?
Methyl alcohol (methanol) is actually not the most acidic compound. Stronger acids, such as hydrochloric acid (HCl) or sulfuric acid (H2SO4), have lower pKa values and are more acidic than methanol. Methanol is a weak acid compared to these stronger acids.
What functional group is present in methyl stearate?
Its functional group is carboxylic acid i.e. COOH. Having chemical formula C17H35COOCH3 Colorless crystals melting at 39°C; soluble in alcohol and ether, insoluble in water; used as an intermediate for stearic acid manufacture.
Why Oxalic acid is stonger than malonic acid?
Oxalic acid is stronger than malonic acid due to the presence of two carboxylic acid functional groups that can readily dissociate to release two protons, making it a stronger acid. Malonic acid has only one carboxylic acid group, so it can release only one proton, making it a weaker acid compared to oxalic acid.
Methyl alcohol and pure acetic acid mixed?
When methyl alcohol and pure acetic acid are mixed, they can react to form methyl acetate. This reaction is an esterification process that results in the formation of an ester along with water as a byproduct. Methyl acetate is a commonly used solvent and is also used in the production of various chemicals.
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.
Is Butyl Alcohol a reactants used to make methyl butyrate?
the reactants are methanol and butyric acid
What alcohol and acid is Isopentyl Isovalerate made of?
Isopentyl isovalerate is an ester synthesized from isopentyl alcohol and isovaleric acid. Isopentyl alcohol, also known as isopentanol or 3-methyl-1-butanol, is a type of alcohol, while isovaleric acid is a type of carboxylic acid.
The most acidic compound is methyl alcohol?
Methyl alcohol (methanol) is actually not the most acidic compound. Stronger acids, such as hydrochloric acid (HCl) or sulfuric acid (H2SO4), have lower pKa values and are more acidic than methanol. Methanol is a weak acid compared to these stronger acids.
Is Methylparaben an alcohol derivitive?
No, it is the methyl ester of p-hydroxybenzoic acid.
What functional group is present in methyl stearate?
Its functional group is carboxylic acid i.e. COOH. Having chemical formula C17H35COOCH3 Colorless crystals melting at 39°C; soluble in alcohol and ether, insoluble in water; used as an intermediate for stearic acid manufacture.
Why Oxalic acid is stonger than malonic acid?
Oxalic acid is stronger than malonic acid due to the presence of two carboxylic acid functional groups that can readily dissociate to release two protons, making it a stronger acid. Malonic acid has only one carboxylic acid group, so it can release only one proton, making it a weaker acid compared to oxalic acid.
Is oleic acid soluble in ethyl alcohol?
Yes
Methyl alcohol and pure acetic acid mixed?
When methyl alcohol and pure acetic acid are mixed, they can react to form methyl acetate. This reaction is an esterification process that results in the formation of an ester along with water as a byproduct. Methyl acetate is a commonly used solvent and is also used in the production of various chemicals.
What is Malonic acids role with respect to succinate dehydrogenase?
Malonic acid is a competitive inhibitor of succinate dehydrogenase.
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.
Is malonic acid a diprotic acid?
Yes, malonic acid is a diprotic acid because it has two ionizable hydrogen atoms that can donate protons in aqueous solution.
Is malonic acid soluble in methanol?
Soluble in cold water, methanol.Partially soluble in acetone.Very slightly soluble in diethyl ether.Solubility in methanol @ 20 deg.: 82.70 g/100 g solventSolubility in diethyl ether@ 20 deg. C: 0.84 g/100 g solventSolubility in ethanol @ 20 deg. C: 45.53 g/100 g solventSolubility in acetone @ 20 deg. C: 17.75 g/100 g solventSolubility in dioxane @ 20 deg. C: 22.70 g/100 g solventSolubility in water @ 20 deg. C: 55. 8 g/100 g solventPractically insolubility in benzene
